Bcl-2 Family Evolutionary Conservation: Comparison
View Latest Version
Please note this is a comparison between Version 1 by Marc Kvansakul and Version 3 by Marc Kvansakul.

Intrinsic apoptosis, the response to intracellular cell death stimuli, is regulated by the interplay of the B-cell lymphoma 2 (Bcl-2) family and their membrane interactions. Bcl-2 proteins mediate a number of processes including development, homeostasis, autophagy, and innate and adaptive immune responses and their dysregulation underpins a host of diseases including cancer. The Bcl-2 family is characterized by the presence of conserved sequence motifs called Bcl-2 homology (BH) motifs, as well as a transmembrane region, which form the interaction sites and intracellular location mechanism, respectively. Bcl-2 proteins have been recognized in the earliest metazoans including Porifera (sponges), Placozoans, and Cnidarians (e.g., Hydra). A number of viruses have gained Bcl-2 homologs and subvert innate immunity and cellular apoptosis for their replication, but they frequently have very different sequences to their host Bcl-2 analogs. Though most mechanisms of apoptosis initiation converge on activation of caspases that destroy the cell from within, the numerous gene insertions, deletions, and duplications during evolution have led to a divergence in mechanisms of intrinsic apoptosis. Currently, the action of the Bcl-2 family is best understood in vertebrates and nematodes but new insights are emerging from evolutionarily earlier organisms.

  • apoptosis
  • Bcl-2
  • evolution
  • mechanism
  • structure analysis

1. Introduction

Apoptosis or programmed death of cells has played a significant role in metazoan evolution and prioritizes the organism over individual cells [1][2][1,2]. One form of apoptosis, intrinsic or mitochondrial regulated apoptosis, is initiated by a range of intra- and extracellular stimuli to regulate developmental and homeostatic processes [3]. The genes most closely associated with intrinsic apoptosis are the B-cell lymphoma 2 (Bcl-2) family and have been identified in the basal clades of metazoans, including Porifera (sponges), Cnidaria (anemones, corals, jellyfish), and Placozoa [4][5][4]. In mammals, these genes regulate the integrity of mitochondria where they either initiate the release of apoptogenic factors or prevent this process from occurring (Figure 1). The threshold for cell fate is mediated by antagonism between prosurvival and proapoptotic members of the Bcl-2 family [6][5] and this fundamental interaction is conserved from sponges [7][6] to man [8][7]. Evolutionary gene losses have led to simplification of this process in some organisms, such as insects and nematodes (Figure 1b). Viruses have also acquired Bcl-2 genes to facilitate replication and counter infected cells’ ability to orchestrate intrinsic apoptosis as part of antiviral defense mechanisms [9][8]. The molecular basis of the interaction between prosurvival and proapoptotic proteins relies on their conserved sequences and structures [8][7].
Biomolecules 10 00128 g001 550
Figure 1. Mechanisms of Bcl-2 regulated apoptosis. Simplified apoptosis schemes showing the role of Bcl-2 proteins in apoptosis initiation differ between mammals (a) and nematodes (b). The Bcl-2 family members are indicated for M. musculus. Nematodes have a simplified activation of apoptosis where the BH3-only protein EGL–1 binds the sole prosurvival protein in the C. elegans genome CED-9. This event releases the caspase activating protein CED–4 to initiate the caspase cascade. In mammalian apoptosis, the BH3-only group of proteins antagonize the prosurvival Bcl-2 proteins releasing Bax, Bak, or Bok to oligomerize and form pores in mitochondria causing mitochondrial outer membrane permeabilization (MOMP). Cytochrome c release from the mitochondrion triggers the mammalian equivalent of CED-4, APAF-1, to oligomerize and initiate the activation of downstream caspases.
Bcl-2 proteins (Table 1) are identified by the presence of up to four conserved linear sequence motifs or domains comprising about 20 residues and known as Bcl-2 Homology (BH) motifs (Figure 2) [8][10][7,9].
Biomolecules 10 00128 g002 550
Figure 2. Sequence-structure analysis of Bcl-2 family members from sponges to man. (a) Structure-based sequence alignment of metazoan and viral Bcl-2 family members. Structurally equivalent residues are aligned. In (a), sequence–structure alignment shows prosurvival and proapoptotic Bcl-2 proteins share key sequence features. Sequences aligned: H. sapiens Bcl-xL; G. cydonium BHP2; C. elegans CED-9; Mus musculus Bax; Myxoma virus M11L; Vaccinia virus N1L. Sequence–structure alignment was performed using Dali [11][85] and the secondary structure is indicated by the colored bars. The extent of the Bcl-2 homology (BH) motifs and transmembrane region (TM) is indicated by bars above the sequence and the helices below the sequences. (b) Table of sequence identities and similarities for the sequences in (a) given as percentage sequence identity/sequence similarity in each entry. Notably, the viral Bcl-2 proteins have little recognizable shared sequence identity with mammalian Bcl-2 proteins. (c) Profiles of BH and TM regions from Bax sequences representing bilaterians (Lepisosteus oculatis, Strongylocentrotus purpuratus, Ciona intestinalis), cnidarians (H. vulgaris, Acropora digitifera), placozoa (T. adhaerens), and porifera (A. queenslandica). The height of each stack represents the conservation and the residue frequencies are represented by their height as determined by the program Skylign [12][86]. These indicate that the BH4 motif is a relatively weak and poorly conserved motif when compared to the BH1–BH3 motifs. Uniprot sequence and PDB IDs, hsBcl-xL: Q07817, 1R2D; gcBHP2: Q967D2, 5TWA; ceCED-9: P41958, 1OHU; mmBax: Q07813, 5W62; Myxoma virus M11L: Q77PA8, 2JBX; Vaccinia virus N1L: P21054, 2I39.
Table 1. Summary of Bcl-2-related proteins and their activities.
Name(s) Species Functions References
Bcl-2 H. sapiens Prosurvival [13][14][10,11]
Bcl-w H. sapiens Prosurvival [15][16][17][12,13,14]
Bcl-xL H. sapiens Prosurvival [18][19][15,16]
Mcl-1 H. sapiens Prosurvival [20][21][17,18]
Bfl-1/A1 H. sapiens Prosurvival [22][23][19,20]
Bcl-b H. sapiens Prosurvival [24][25][21,22]
Boo/Diva M. musculus Prosurvival [24][26][21,23]
NRZ D. rerio Prosurvival [27][28][24,25]
Bak H. sapiens Proapoptotic [29][30][26,27]
Bax H. sapiens Proapoptotic [31][32][28,29]
Bok H. sapiens Proapoptotic [33][30]
Bad H. sapiens Proapoptotic [34][31]
Bid H. sapiens Proapoptotic [35][32]
Bik H. sapiens Proapoptotic [36][33]
Bim H. sapiens Proapoptotic [37][34]
Bmf H. sapiens Proapoptotic [38][35]
Hrk H. sapiens Proapoptotic [39][36]
Noxa H. sapiens Proapoptotic [40][37]
Puma H. sapiens Proapoptotic [41][38]
Beclin H. sapiens Proautophagic [42][39]
Bcl-wav D. rerio Proapoptotic [43][44][40,41]
Buffy D. melanogaster Proapoptotic [45][42]
DeBcl D. melanogaster Prosurvival [46][43]
BHRF1 Epstein–Barr virus Prosurvival [47][48][44,45]
KsBcl-2 Kaposi Sarcoma herpesvirus Prosurvival [49][46]
E1B19K Human adenovirus Prosurvival [50][47]
M11 mγ68 herpesvirus Prosurvival [51][52][48,49]
A179L African swine fever virus Prosurvival [53][54][50,51]
F1L Vaccina virus, variola virus Prosurvival [55][56][52,53]
DPV022 Deer poxvirus Prosurvival [57][58][54,55]
M11L Myxomavirus Prosurvival [59][60][56,57]
FPV039 Fowl poxvirus Prosurvival [61][62][58,59]
CNP058 Canary poxvirus Prosurvival [63][64][60,61]
SPPV14 Sheep poxvirus Prosurvival [65][62][661]
 TANV16L Tanapoxvirus Prosurvival [672]
ORFV125 Orf virus Prosurvival [68][69][63]
GIV66 Grouper iridovirus Prosurvival [70][71][64,65]
N1 Vaccinia virus Prosurvival, NF-κb [72][73][66,67]
A46 Vaccinia virus NF-κb [74][75][68,69]
A49 Vaccinia virus NF-κb [76][77][70,71]
A52 Vaccinia virus NF-κb [78][72]
B14 Vaccinia virus NF-κb [78][72[79],73]
K7 Vaccinia virus NF-κb, IFN signaling [80][74[81],75]
LB-Bcl-2 L. baicalensis Prosurvival [82][76]
LB-Bak-2 L. baicalensis Proapoptotic [7][82][6,76]
BHP1 G. cydonium Prosurvival [83][77]
BHP2 G. cydonium Prosurvival [7][83][6,77]
trBcl-2L1 T. adherens Prosurvival [843]
trBcl-2L2 T. adherens Prosurvival [843]
trBcl-2L3/trBax T. adherens Proapoptotic [843]
trBcl-2L4/trBak T. adherens Proapoptotic [843]
Hy-Bcl-2-4 H. vulgaris Proapoptotic [854]
Hy-BH3-only-2 H. vulgaris Proapoptotic [854]
Hy-Bak1 H. vulgaris Proapoptotic [854]
Hy-Bax H. vulgaris Proapoptotic [854]
EGL-1 C. elegans Proapoptotic [86][87][79,80]
CED-9 C. elegans Prosurvival [88][89][81,82]
vMIA Cytomegalovirus Prosurvival [90][91][83,84]
The Bcl-2 proteins fold to form a distinct helical bundle structure where the core of the α–helical bundle is composed of a central hydrophobic helix (helix α5) that forms a scaffold for packing up to eight α-helices (Figure 2 and Figure 3). In a feature maintained from sponges to man [10][9], the Bcl-2 fold brings the BH regions into close proximity to assemble the canonical BH3-binding groove where an antagonist BH3 motif binds (Figure 3b,c). Whilst this “in-groove” interaction mechanism appears to be the primary mode of interaction for Bcl-2-mediated control of apoptosis, alternative modes have been proposed including a site spanning helices α1 and α6 [92][87] and the BH4 motif [93][88]. Furthermore, nonapoptotic roles including modulation of NF-κB signaling are also not mediated via an in-groove mechanism [94][89]. BH motifs are recognizable from the earliest metazoan Bcl-2 proteins but may be absent in viral proteins. The sequence signatures of each of the four BH motifs (BH1–BH4) differ (Figure 2c) and are found in the order from the N-terminus: BH4, BH3, BH1, BH2 (Figure 2a) and for prosurvival proteins are normally located on the same exon while the gene structure for the proapoptotic proteins is more complex. The presence of a BH3 motif is a key feature of the proapoptotic proteins and required for their proapoptotic activity [10][95][9,90], whereas some of the prosurvival proteins do not feature the BH3 motif. In addition to the presence of the BH motifs, many Bcl-2 proteins bear a C-terminal transmembrane (TM) region that is located on a separate exon. The TM region targets these proteins to intracellular membranes including the nuclear envelope, mitochondrial inner and outer membranes, Golgi apparatus, lysosomes, ER, and peroxisomes [96][91]. However, it is Bcl-2 family action at the mitochondrial outer membrane (MOM) that is the most central mechanistic feature for intrinsic apoptosis. Both the gene structure and synteny of Bcl-2 proteins are well conserved across phyla [97][92].
Biomolecules 10 00128 g003 550
Figure 3. Evolutionary structure conservation in the Bcl-2 family and their complexes. Ribbon representation of the 3D structures of prosurvival and proapoptotic Bcl-2 family members and their complexes are shown. The helical bundle Bcl-2 structure occurred early in evolution and changed little over evolutionary time scales. (a) H. sapiens Bcl-xL (PDB 1R2D) with BH1–BH4 motifs colored in orange, green, cyan, and red as shown in the sequence–structure alignment of Figure 2a. (b) H. sapiens Bcl–xL (PDB 1R2D) shown as grey surface with canonical ligand-binding groove shaded in magenta, (c) BHP2 from the sponge G. cydonium Bcl-2, BHP2 (PDB 5TWA) magenta, LB–Bak sky blue. The canonical ionic interaction between the conserved Arg from prosurvival Bcl-2 and conserved Asp from the BH3 motif of prodeath Bcl-2 as well as the four conserved hydrophobic residues from the Bak BH3 motif are shown as sticks. (d) M. musculus Bax (PDB 5W62) yellow, (e) H. sapiens Bcl-b:Bim complex (PDB 4B4S), (f) C. elegans CED-9: EGL-1 complex, CED-9 (navy) with EGL–1 (sand) in the binding groove (PDB 1TY4). (g) Myxoma virus Bcl-2 M11L (PDB 2JBX) cyan, (h) Vaccinia virus N1L (PDB 2I39) salmon. Monomeric N1 is shown in the same orientation as in (a), and the functionally relevant dimer is shown rotated by 90o around the vertical axis. In (a), the extent of the BH motifs is indicated as ribbon colored as in Figure 2a and the helices α1–α8 are also indicated. The structures were aligned on human Bcl-xL and the orientation for all structures is the same as that in (a). The N and C termini are indicated.
Our current understanding of intrinsic apoptosis is mainly derived from investigations of mouse, human, nematode (Caenorhabditis elegans), and fly (Drosophila melanogaster) apoptosis. These studies have shown the Bcl-2 family consists of two phylogenetically distinct groups of proteins: those that share the Bcl-2 fold [95][98][90,93] that are either prosurvival or proapoptotic and the proapoptotic intrinsically disordered ‘BH3-only’ proteins, that bear only the BH3 motif [10][9]. The BH3-only proteins are upregulated in response to diverse apoptotic stimuli [99][94] and their principal role is to antagonize the prosurvival proteins [10][9], but apoptosis also occurs in their absence [100][95]. Notwithstanding the conservation in the Bcl-2 family, there are substantial differences in Bcl-2-regulated apoptosis mechanisms. In mammals, there are nine multimotif Bcl-2 paralogs (six prosurvival Bcl-2, Bcl-xL, Bcl-w, Mcl-1, A1, Bcl-B, and three proapoptotic Bax, Bak, and Bok) and eight BH3-only proteins (Bim, Bad, Bmf, Bid, Bik, Noxa, Puma, Hrk) (Table 1) that regulate intrinsic apoptosis through a network of specific binding interactions that control the integrity of the MOM [8][7] (Figure 1). A key step is Bax, Bak, or Bok oligomerization at the mitochondrial membrane that results in formation of membrane pores releasing cytochrome c to activate the caspase cascade. In contrast to mammals, MOM permeabilization (MOMP) and cytochrome c do not play a role in initiation of apoptosis in ecdysozoans C. elegans (Figure 1) or D. melanogaster [8][45][101][7,42,96] (Figure 1). Combined, these results indicate the interactions of the Bcl-2 proteins have been maintained over the course of evolution.
The role of prosurvival Bcl-2 proteins is not limited to regulation of apoptosis; other functions have been proposed in processes as divergent as autophagy, calcium homeostasis regulation, and metabolism [102][103][104][97,98,99]. The most well-understood process at a molecular level of these nonapoptotic roles is that of autophagy. Both Bcl-2 and Bcl-xL are able to bind the autophagy regulator Beclin-1 via a mechanism closely mimicking the canonical in-groove interaction with BH3-only proteins [52][105][106][49,100,101]. Beclin-1 has significant differences from the BH3-only proteins. In addition to being much longer (450 residues) than a typical BH3-only protein (54–198 residues for human BH3-only proteins), Beclin-1 has its BH3-like motif located in an unstructured N-terminal region [107][102] with the BH3 motif spread over the junction of two exons. In addition to its unstructured N-terminal region Beclin-1 bears a coiled coil domain and a folded evolutionary conserved domain [108][103]. The spread of the BH3 motif over two exons differentiates Beclin-1 from the BH3-only proteins where apart from Bid the BH3 occurs in the second-to-last exon. The molecular basis of Bcl-2 proteins in nonapoptotic functions remains to be delineated.
Dysfunctional apoptosis is one of the hallmarks of disease like cancer [109][104] and metazoans have coevolved with this disease [110][105]. While neoplasms in many vertebrates are well known [110][105], they have also been discovered in the early metazoans H. vulgaris [111][106], coral Acropora palmata [112][107], and molluscs [113][108], and in the case of hydra, occur as a result of dysregulation of apoptosis [111][106]. While some cancers are unique to a species, others occur across multiple species [114][109] and resistance to apoptosis is likely to be a central feature. There is strong interest in developing a molecular understanding in Bcl-2 function, interactions, and structures [8][7] but currently there is only a limited number of studies on early metazoan Bcl-2-regulated apoptosis [7][115][6,110]. However, these initial studies strongly suggest conservation of structures and mechanisms across metazoan history. Exactly how intrinsic apoptosis is manifested at a molecular level varies according to the organism, but all mechanisms rely on loss of prosurvival activity to initiate apoptosis. Consequently, there has been a drive to explore the interactions of this family and elucidate the network of functions they regulate.

2. Virus-Encoded Bcl-2 Homologs

The importance of the Bcl-2 family in homeostatic regulation has been exploited by viruses with many viral genomes containing a Bcl-2 protein, and in some instances, multiple Bcl-2 proteins [9][8]. Sequence, structural, and functional homologs of Bcl-2 are found in Herpesviridae as well as Nucleocytoplasmic Large DNA Viruses (NCLDVs) such as Asfarviridae and Iridoviridae [9][8]. Many of these virus-encoded Bcl-2 family members display substantial differences with regards to their sequence (Figure 2a,b) and interaction profiles to their mammalian proapoptotic Bcl-2 family counterparts as well as their overall structure, owing to the more rapid pace at which these proteins have evolved as part of a host–pathogen interface [9][116][8,111]. The first viral Bcl-2 homologs were identified in adenovirus [117][112] and the γ-herpesvirus Epstein–Barr virus (EBV) [47][44]. Adenoviral E1B19K was shown to be a potent inhibitor of apoptosis and could be interchanged with Bcl-2 during cellular transformation [117][112]. Whilst the vast majority of virus-encoded apoptosis regulatory Bcl-2 proteins act by utilizing the canonical ligand-binding groove to sequester proapoptotic Bcl-2 family members, it has become apparent that this is not the sole mechanism utilized. In addition to binding proapoptotic proteins, viruses may target host prosurvival Bcl-2 proteins through the BH3-binding groove in a manner similar to but not identical to a BH3 motif, and Hepatitis B virus X protein was shown to engage the groove of Bcl-xL allowing viral replication to proceed [118][113].

2.1. Bcl-2 Homologs Encoded by Herpesviridae

Numerous Herpesviridae encode Bcl-2-like proteins such as BHRF1 from EBV, one of the earliest identified viral Bcl-2 homologs. BHRF1 adopts the classical Bcl-2 fold and utilizes the canonical ligand-binding groove to engage proapoptotic BH3 motif ligands [48][119][45,114]. BHRF1 was shown to prolong survival of cells [47][120][44,115], which is linked to its ability to engage proapoptotic Bcl-2 members Bim [121][116] and Bak [119][114]. An unusual herpesviral Bcl-2 homolog is found in murine γ–herpesvirus 68, M11 [122][117]. M11 is a potent inhibitor of TNFα and Fas-induced apoptosis, and was shown to bind multiple proapoptotic Bcl-2 proteins including Bim, Bak, and Bax [106][101]. However, M11 also binds the autophagy regulator Beclin-1, which bears a BH3-like motif, with nanomolar affinity (KD = 40 nM), which is bound via the canonical ligand-binding groove [106][101]. Indeed, functional studies suggest that autophagy may be the primary cell death pathway targeted by M11 [52][49]. Although the majority of herpesvirus-encoded Bcl-2 proteins target intrinsic apoptosis, γ68-encoded M11 clearly shows that other cell death pathways such as autophagy can also be viable targets. Indeed, M11 is not an exception, and adenoviral E1B19K was shown to be an autophagy inhibitor via engagement of Beclin-1 [123][118], as was the asfarvirus African swine fever virus (ASFV) A179L (see below).

2.2. Poxvirus Bcl-2 Homologs

The Poxviridae  are a large superfamily of viruses amongst the NCLDVs comprising numerous families that are characterized by their relatively large genomes (130–360 kb) that frequently encode functional and structural homologs of Bcl-2 [124]. Most notable for human disease among the pox viruses are Variola virus, the causative agent of smallpox, and Vaccinia virus, which provides the basis for smallpox vaccine. Vaccinia virus (VACV) is the prototypical member of the Orthopoxviridae and encodes for prosurvival F1L. VACV F1L is a potent inhibitor of intrinsic apoptosis, but displays no detectable sequence identity with mammalian Bcl-2 [125][126][119,120]. Nevertheless, structural studies revealed that VACV F1L adopts a Bcl-2 fold, albeit with a previously not observed domain-swapped topology that rendered VACV F1L a constitutive dimer [56][127][53,121]. This unusual topology is paired with a remarkably restricted ligand-binding profile, with VACV F1L only engaging Bim, Bak, and Bax. Interestingly, similar domain swapping was subsequently also observed during Bax and Bak oligomerization [128][122], suggesting that the structural plasticity observed amongst the virus-encoded Bcl-2 proteins is also pivotal for the function of metazoan family members. In the context of a live viral infection, F1L inhibits Bim to prevent premature host cell apoptosis [127][121] and replaces Mcl-1 activity [129][123]. An extended unstructured N-terminal section prior to the Bcl-2 fold [130][124] may be involved in apoptosis regulation but results are conflicting [130][131][132][124,125,126]. Despite being closely related to VACV F1L, the Variola virus (VAR) F1L homolog does not bind Bim; instead it binds Bid, Bak, and Bax [133][127], and only counters Bax-mediated apoptosis. The domain-swapped Bcl-2 topology is not restricted to the Orthopoxviridae, with deerpoxvirus-encoded DPV022 [58][57][55] and orfvirus OFV125 [69] also adopting this unusual fold [54]. Amongst the Leoporipoxviridae, myxomavirus encodes for antiapoptotic M11L (Figure 3d), a potent inhibitor of intrinsic apoptosis [134][128]. Despite lacking detectable sequence identity to cellular Bcl-2 or Bcl-xL, M11L adopts a Bcl-2 fold [60][135][57,129] (Figure 2a,b and Figure 3g,h) and sequesters Bax and Bak to prevent apoptosis [60][57], unlike VACV F1L which operates via Bim neutralization [127][121]. Other poxvirus-encoded vBcl-2 members include fowlpox FPV039 [61][62][58,59] and canarypox virus (CNPV058) [64][61], sheep poxvirus [62][65][1], tanapoxvirus [2] and orf virus ORFV125 [68][69][63]. Outside the herpes and Poxviridae, ASFV encodes A179L [136][130], a Bcl-2 homolog that uses the canonical ligand-binding groove to engage all major host proapoptotic Bcl-2 members [54][51] as well as Beclin-1 [137][131], thus acting as a dual apoptosis/autophagy inhibitor [53][138][50,132]. Amongst the Iridoviridae, grouper iridovirus (GIV) harbors prosurvival GIV66 [71][65] that only binds Bim [70][64], and forms a novel noncovalent dimeric Bcl-2 architecture which leads to an occluded ligand-binding groove [70][64] and dimer dissociation upon Bim binding.
While numerous Poxviridae encode Bcl-2 homologs that inhibit apoptosis, it has become apparent that another subset of poxviral Bcl-2 proteins exists that also modulate other functions. This group includes VACV N1 which, like M11L, has little shared sequence identity with mammalian Bcl-2 proteins (Figure 2b) but is a structural homolog (Figure 3g). N1 is a dual inhibitor of intrinsic apoptosis that adopts a dimeric Bcl-2 fold (Figure 3h) [73][139][67,133] where an additional interaction site enables modulation of NF-κB signaling that is regulated independently of the canonical Bcl-2 groove [94][89]. Other VACV-encoded NF-κB modulatory Bcl-2 proteins include A46 [74][140][68,134], A49 [76][70], A52, B14 [78][72], and K7 [81][75]. Despite targeting NF-κB signaling, substantial structural and mechanistic differences are evident across this group of Bcl-2 proteins. Although A52 and B14 utilize helices α1 and α6 to form a similar interface [78][72] as N1, the angle of orientation between the constituent monomers varies between the three proteins.
Intriguingly, while apoptosis inhibitory Bcl-2 members are found in Herpes, Pox, Asfar, and Iridoviridae, more specialist functions are not widely found. Although several herpesviruses as well as ASFV harbor Bcl-2 homologs with autophagy inhibitory activity, no poxvirus has been shown to inhibit autophagy via a Bcl-2 homolog. Conversely, the NF-κB inhibitory activity found in poxvirus-encoded Bcl-2 homologs is not found outside the Poxviridae. Whether or not these differences are attributable to the unique and fundamentally different life cycles and primary sites of infection remains to be established. These findings differentiate the viral Bcl-2 proteins from those in metazoans but indicate the diversity of interactions possible with the Bcl-2 fold.

3. The Nonmammalian Bcl-2 Family

Of the four nonbilaterian basal clades of metazoans, Porifera, Placozoa, Cnidaria, and Ctenophora, multiple orthologous and paralogous Bcl-2 family members have been discovered in the genomes of organisms from Porifera, Placozoa and Cnidaria, but have not yet been identified in ctenophores and are absent altogether in some ecdysozoans [65][141]. In contrast to higher organisms and viruses, experimental evidence for the function of the Bcl-2 family in basal metazoans is relatively sparse. Recent sequence, structural, and biochemical evidence gained from poriferan [7][6], placozoan [843], and cnidarian [110][1154][85] Bcl-2 family members are elucidating the mechanisms of apoptosis in basal metazoans. Furthermore, these results strongly suggest the molecular basis of intrinsic apoptosis determined by the structures, interactions, and intracellular localization of Bcl-2 proteins was foundational in metazoan evolution.
Sponges are currently considered the sister group to metazoans [142][143][135,136] and multiple Bcl-2 family proteins have been discovered in members of this phylum; for example, the genome of Amphimedon queenslandica contains seven potential Bcl-2 proteins [144][137], though little is known of their function. The demosponge Lubormirskia baicalensis harbors putative prosurvival and proapoptotic Bcl-2 proteins LB-Bcl-2 and LB-Bak-2 [82][76], and two Bcl-2 proteins, BHP1 and BHP2, have been identified in the sponge Geodium cydonium [83][77]. Structural and biochemical studies on BHP2 showed that a BH3 peptide derived from the BH3 region of L. baicalensis Bak-2 bound in the groove of BHP2 and many of the molecular features elucidated in mammalian Bcl-2 interactions were maintained [7][6]. Though the topology of BHP2 closely resembles those of other Bcl-2 proteins (Figure 2 and Figure 3), a structure–phylogenetic analysis showed there were relatively subtle differences suggesting BHP2 has unique binding features when compared to mammalian and viral Bcl-2 proteins [7][6]. These findings not only indicate the structure conservation but the evolutionary conservation of the intermolecular interactions of the BH3 motif:Bcl-2-in-groove interaction between prosurvival and proapoptotic Bcl-2 proteins from sponges to man.
The placozoan Trichoplax adhaerens has four putative Bcl-2 fold proteins in its genome [145][138] including two putative proapoptotic proteins, Bax (trBcl-2L3 or trBax) and Bak (trBcl-2L4 or trBak), and two prosurvival proteins, trBcl-2L1 and trBcl-2L2 [843]. TrBax is inhibited by human Bcl-2, suggesting the BH3-in-groove interaction is conserved. The putative role of trBak in T. adhaerens is somewhat different from that in humans, where it antagonizes the prosurvival activity of trBcl-2L1 and trBcl-2L2 rather than inducing cytochrome c loss from mitochondria, and thus it has been hypothesized that trBak effectively adopts the role of a BH3-only protein in mammals; however, further investigation is required to establish this proposal as no detailed interaction studies were undertaken. As for the case of G. cydonium, the underlying conservation of the Bcl-2:Bax interaction was demonstrated by the inhibition of trBax by human prosurvival proteins.
The BH3-only proteins play a key role in mammalian apoptosis where they antagonize the action of prosurvival proteins (Figure 1), but their presence has not been detected in the genomes of Porifera or Placozoa. However, candidates for BH3-only proteins have been detected in the cnidarian H. vulgaris [146][147][139,140] in addition to Bcl-2 fold sharing prosurvival proapoptotic Bcl-2 proteins. Potential BH3-only proteins have been identified in H. vulgaris using a yeast two-hybrid screen [115][110]. The relatively short sequence of the BH3-only motif with essentially only a highly conserved Leu and absolutely conserved Asp four residues downstream has made it difficult to identify bona fide BH3-only sequences by sequence alone, making it necessary for biochemical verification [9,141][104][148][85]. In addition to the four proposed BH3-only proteins in  H. vulgaris, there are nine putative Bcl-2 family members including two Bak-like and seven Bcl-2 like sequences [110][1154][85]. Structural and biochemical analysis revealed that Hy-Bcl-2-4 acts as a prosurvival Bcl-2 protein, and together with the proapoptotic Hy-BH3-only-2, Hy-Bak1 and Hy-Bax forms a core intrinsic apoptosis machinery that mirrors those in mammalian systems [854][65]. Although further studies are required to establish the exact functional relationships for these proteins, the findings of Lasi et al. [115][110] point to a complex signaling network for the Bcl-2 proteins even in the earliest of metazoans.
The genetic [101][96] and molecular and structural [86][149][79,142] foundations of Bcl-2-regulated apoptosis were established in the ecdysozoan C. elegans (Figure 1, Figure 2a and Figure 3f). Since these discoveries, the basis of prosurvival, proapoptotic, and BH3-only protein interaction has been verified in other organisms. The genomes of the lophotrochozoans Schmidtea mediterranea, S. japonicum, and S. mansoni bear multiple Bcl-2-like proteins including BH3-only components [150][151][143,144]. Investigation of apoptosis in platyhelminths (S. mediterranea and Dugesia dorotocephala) identified Bak and Bcl-2 orthologs and experimental data mitochondrial cytochrome c release is associated with MOMP and caspase activation [151][144]. Binding between the Bcl-2 proteins and BH3-only proteins in S. japonicum was established using immunoprecipitation experiments [150][143]. Mutational, structural, and biochemical studies defined the binding mode as similar to other Bcl-2:BH3 interactions and cytochrome c release on treatment with a BH3 motif peptide [150][143]. Combined, these studies on lophotrochozoans indicate that, in contrast to ecdysozoans, a tripartite mechanism exists with prosurvival, proapoptotic, and BH3-only proteins triggering MOMP and cytochrome c release to initiate intrinsic apoptosis in these organisms. The conclusion from these studies is that intrinsic apoptosis signaling in the protostomes has been modified by gene loss in some organisms but the underlying tripartite mechanism leading to MOMP is preserved in others and the MOM interaction remains central.
Experiments on the cytosolic extracts from the echinoderms Strongylocentrotus purpuratus (purple sea urchin) and Dendraster excentricus (sand dollar) indicate caspase activation could be induced with cytochrome c, suggesting mitochondrial-regulated apoptosis occurs in the deuterostomes in a similar way to that in the protostomes [151][144]. However, others have suggested that apoptosis activation in echinoderms may not involve cytochrome c release from mitochondria as cytochrome c is not apparently necessary for Apaf-1-activated apoptosis in the starfish Asterina pectinifera [152][145]. In the nonmammalian vertebrates, the molecular basis of apoptosis is probably best defined in zebrafish, Danio rerio, where all three groups of the tripartite Bcl-2 family have been identified [153][146]. D. rerio has an extensive network of Bcl-2 proteins, but as yet there are relatively few details on the mechanism of action even in this well-studied model organism [154][147]. Genome duplication events in teleost fish [155][148] have given rise to many Bcl-2 paralogs in D. rerio [102][97], but the molecular basis of apoptosis is likely similar to that in mammals [28][25]. Structural studies on D. rerio NRZ show the structure and mode of BH3 interaction is near identical to other organisms [28][25]. These studies establish Bcl-2 signaling in deuterostomes share many aspects with those from the protostomes and establish the basis for intrinsic apoptosis in the bilaterians.

4. The Role of Mitochondrial Membrane Interactions

The defining event of intrinsic apoptosis in mammals is release of cytochrome c from the mitochondrial intermembrane space through supramolecular pores formed by Bax, Bak, or Bok oligomerization on the MOM [156][149] (Figure 1). Crucial to this action is the presence of a TM anchor and most members of the Bcl-2 family bear tail anchors, including BH3-only proteins, [157][150] necessary both for their localization at the MOM [6][5] and apoptotic activity [158][151]. TM anchor deletion mutants of Bax and Bak lose their apoptotic abilities [159][152], suggesting the MOM as an activator of Bax/Bak [160][153]. Similarly, deletion of the TM region of prosurvival Bcl-xL decreases its prosurvival activity [158][151]. The most striking feature of the TM regions is their poor sequence conservation [161][154]. Figure 2c illustrates the relatively weak conservation of the TM region compared to the BH motifs in Bax sequences. In mammalian apoptosis, cofactors such as the β-barrel Voltage Dependent Anion Channel-2 (VDAC2) may be important in Bax/Bak membrane recruitment [162][155], but this has not yet been demonstrated in basal metazoan apoptosis. While most investigations have focused on apoptosis in the mouse or humans, MOM association has also been observed for Bcl-2 proteins from placozoans, hydra, and viral proteins, indicating the fundamental nature of this activity to Bcl-2 action.
The structures of the proapoptotic proteins Bax, [32][29] Bak, [30][27] and Bok [163][164][156,157] have an essentially identical core that suggests a common mode of action; however, their subcellular localization and dynamics differ significantly [96][91]. The crystal structure of mouse Bax shows that the TM region is helical and packed in the equivalent site as occupied by EGL-1-binding CED-9 (Figure 3d,f). Prior to apoptotic stimuli, Bax is largely cytosolic [165][158], with a fraction being shuttled to the mitochondrion surface [166][159], but subsequent to apoptotic stimuli, Bax accumulates at the MOM [167][168][160,161] via a process that is dependent on its TM residues [169][162]. In contrast to Bax, Bak is constitutively membrane-bound and Bok is only fractionally colocalized with mitochondria [170][163]. The prosurvival protein Bcl-xL translocates Bax from the MOM to the cytosol, and this process is dependent on the BH3-binding groove [166][159] and TM region of Bcl-xL [171][164]. Thus, the proapoptotic proteins have complex membrane interactions and dynamics and emerging data supports a similar view in basal metazoans.
Experimental details on the localization and dynamics of Bcl-2 proteins are now emerging for the placozoan T. adhaerens, and a similar picture of complex dynamic behavior to mammalian Bcl-2 family proteins is emerging [3]. T. adhaerens Bcl-2 proteins are differentially partitioned between mitochondria, ER, and the cytosol, and the TM region is necessary for its membrane localization [3]. TrBcl2L1 is tightly associated with the MOM, while trBcl-2L2 (trMcl-1) and trBcl-2L4 (trBak) are cytosolic and only loosely associated with intracellular membranes [3] in a manner that mirrors the mammalian Bcl-2 proteins. Mammalian prosurvival proteins like the proapoptotic proteins are differentially partitioned between cytosol and membranes. For example, Bcl-2 is membrane integrated and Bcl-xL partitioned between cytosol and membranes. Like its mammalian counterpart, Trichoplax Bax (Bcl-2L3) translocates to the mitochondria and induces cytochrome c release [3]. However, one caveat of these discoveries is that they have been performed in heterologous systems using expression of Trichoplax proteins in mammalian cells and have yet to be confirmed in homologous systems. The studies on T. adhaerens Bcl-2 proteins and their membrane interactions point to the fundamental nature of membrane interactions in their mechanism of action.
Although not all viral Bcl-2 proteins bear an obvious TM region, many do [172][165], and membrane interactions are necessary for their prosurvival activity. This trend closely mirrors what has been observed for mammalian proteins like Bcl-xL. Similarly for the viral Bcl-2 protein F1L, association with mitochondria is necessary for its prosurvival behavior [55][52], and M11L localizes at the mitochondria [134][128] and colocalizes with Bak at the MOM [173][166]. ASFV A179L localizes to mitochondria and ER [138][132]. Although C-terminal anchoring of Bcl-2 proteins is often maintained, there are exceptions; for example, vMIA targets the MOM through its N-terminal region [174][167]. It appears likely that the interaction of Bcl-2 proteins with membranes is fundamental to Bcl-2 function and has been conserved from the earliest metazoans and maintained in viral Bcl-2 proteins.
While MOM localization of Bcl-2 proteins may be conserved, MOMP is not necessarily maintained as a mechanism of activating apoptosis. Ecdysozoans have undergone extensive gene loss [175][168] and have fewer Bcl-2 genes and mechanistic differences from mammalian apoptosis (Figure 1) [176][169]. For example, the sole Bcl-2 protein CED-9 in the nematode C. elegans is TM-anchored to mitochondria like its mammalian counterpart Bcl-2 and although they have closely related structures (Figure 2 and Figure 3) and bind BH3-only proteins in their respective binding grooves, their role in apoptosis mechanisms is not identical [8][7]. CED-9 binds and antagonizes the apical caspase CED-4 and once released from its inhibition by the translationally upregulated BH3-only protein EGL-1 binding CED-9, CED-4 activates the caspase CED-3 [8][101][7,96]. In comparison, Bcl-2 is also localized to the MOM amongst other intracellular membranes [96][91] and binds BH3-only proteins but it does not bind Apaf-1, the mammalian caspase-activating protein corresponding to CED-4. Distinct from the nematode, the role of Bcl-2 proteins in the fly D. melanogaster is less well understood [177][170]. BH3-only proteins have not been found in the genome of D. melanogaster but two Bcl-2 proteins, Debcl and Buffy, have been recognized and it has been shown they interact [45][42] and both localize to the MOM with Buffy additionally found at the ER [178][171]. Thus, although the sequences, structure, and membrane binding may all be conserved elements in the Bcl-2 family, there are key differences in how they are manifested in the activation of caspases.

5. Conclusions

It is not clear how the Bcl-2 family arose; one hypothesis is that it occurred through horizontal gene transfer from a symbiont [179][172], but multiple Bcl-2 genes occurred early in metazoan evolution. Even in the sponges, a phylum considered to be the sister group of all metazoans [142][135], multiple Bcl-2 fold proteins have been identified in genomes, such as that of A. queenslandica [144][137] where seven such proteins were recognized. In contrast to the early appearance of Bcl-2 fold proteins, BH3-only proteins have not yet been identified in Porifera or Placozoa. Ctenophores and some ecdysozoans [65][141] appear to have lost the genes required for Bcl-2-regulated apoptosis altogether (Figure 4a). Emerging results from biophysical and biochemical measurements performed on the nonmammalian Bcl-2 family including those from sponges [7][6], placozoans [843]  and cnidarians [854]  indicate that the basic architecture of intrinsic apoptosis is maintained for these basal metazoans. Structural studies have shown that the molecular details of interactions have been conserved from sponges to man [7][6] and viruses have assimilated Bcl-2 proteins [116][111]. A key difference between sponges, placozoans, and cnidarians is an apparent absence of BH3-only proteins in sponges and placozoans. The essential role of the BH3-only proteins, at least in mammals, is to neutralize the prosurvival proteins to allow the MOM to activate the proapoptotic Bcl-2 proteins [160][153]. Based on these results, a hypothesis for a simple model for intrinsic apoptosis in the absence of BH3-ony proteins could be envisaged as the prosurvival proteins keeping the proapoptotic proteins in check. Alternately, as recently proposed, the Bak-like protein may partially fulfill the role of BH3-only proteins [843]  (Figure 4b). The investigation of the more evolutionary distant members of the Bcl-2 family has exposed the substantial complexity in Bcl-2-mediated signaling at the foundation of metazoan evolution and underscores the pivotal role these proteins play in biology. Functional and mechanistic studies to date have only just begun to unravel the role Bcl-2 has played during the early stages of metazoan life, and future studies are likely to discover new twists to Bcl-2 signaling.
Biomolecules 10 00128 g004 550
Figure 4. Bcl-2-like proteins in basal metazoan clades and potential apoptosis model. (a) Metazoan phylogenetic relationships and the presence or absence of Bcl-2 proteins. The presence or absence of Bcl-2 family members is indicated. (b) A simple model for intrinsic apoptosis in Porifera and Placozoa where BH3-only proteins have not been identified. Experiments have yet to delineate the roles of MOMP and adaptor protein initiation of caspases in their entirety.

References

  1. Koonin, E.V.; Aravind, L. Origin and evolution of eukaryotic apoptosis: The bacterial connection. Cell Death Differ. 2002, 9, 394–404.Chathura D. Suraweera; Denis R. Burton; Mark G. Hinds; Marc Kvansakul; Crystal structures of the sheeppox virus encoded inhibitor of apoptosis SPPV14 bound to the proapoptotic BH3 peptides Hrk and Bax. FEBS Letters 2020, 594, 2016-2026, 10.1002/1873-3468.13807.
  2. Huettenbrenner, S.; Maier, S.; Leisser, C.; Polgar, D.; Strasser, S.; Grusch, M.; Krupitza, G. The evolution of cell death programs as prerequisites of multicellularity. Mutat. Res. 2003, 543, 235–249.Chathura D. Suraweera; Mohd Ishtiaq Anasir; Srishti Chugh; Airah Javorsky; Rachael E. Impey; Mohammad Hasan Zadeh; Tatiana P. Soares da Costa; Mark G. Hinds; Marc Kvansakul; Structural insight into tanapoxvirus‐mediated inhibition of apoptosis. The FEBS Journal 2020, 287, 3733-3750, 10.1111/febs.15365.
  3. Singh, R.; Letai, A.; Sarosiek, K. Regulation of apoptosis in health and disease: The balancing act of BCL-2 family proteins. Nat. Rev. Mol. Cell Biol. 2019, 20, 175–193.Nikolay Popgeorgiev; Jaison D Sa; Lea Jabbour; Suresh Banjara; Trang Thi Minh Nguyen; Aida Akhavan-E-Sabet; Rudy Gadet; Nikola Ralchev; Stéphen Manon; Mark G. Hinds; et al.Hans-Jürgen OsigusBernd SchierwaterPatrick O. HumbertRuth RimokhGermain GilletMarc Kvansakul Ancient and conserved functional interplay between Bcl-2 family proteins in the mitochondrial pathway of apoptosis. Science Advances 2020, 6, eabc4149, 10.1126/sciadv.abc4149.
  4. Strasser, A.; Vaux, D.L. Viewing BCL2 and cell death control from an evolutionary perspective. Cell Death Differ. 2018, 25, 13–20.Suresh Banjara; Jaison D Sa; Mark G. Hinds; Marc Kvansakul; The structural basis of Bcl-2 mediated cell death regulation in hydra. Biochemical Journal 2020, 477, 3287-3297, 10.1042/bcj20200556.
  5. Suresh Banjara; Chathura Suraweera; Mark Hinds; Marc Kvansakul; The Bcl-2 Family: Ancient Origins, Conserved Structures, and Divergent Mechanisms. Neil D. Young; Tiffany J. Harris; Marco Evangelista; Sharon Tran; Merridee A. Wouters; Tatiana P. Soares Da Costa; Nadia J. Kershaw; Robin B. Gasser; Brian J. Smith; Erinna F. Lee; et al.W. Douglas Fairlie Diversity in the intrinsic apoptosis pathway of nematodes. Communications Biomlolecules gy 2020, 10, 128, 10.3390/biom10010128., 3, 1-12, 10.1038/s42003-020-01208-5.
  6. Shamas-Din, A.; Kale, J.; Leber, B.; Andrews, D.W. Mechanisms of action of bcl-2 family proteins. Cold Spring Harb. Perspect. Biol. 2013, 5.
  7. Caria, S.; Hinds, M.G.; Kvansakul, M. Structural insight into an evolutionarily ancient programmed cell death regulator—The crystal structure of marine sponge BHP2 bound to LB-Bak-2. Cell Death Dis. 2017, 8, e2543.
  8. Kvansakul, M.; Hinds, M.G. The Bcl-2 family: Structures, interactions and targets for drug discovery. Apoptosis 2015, 20, 136–150.
  9. Kvansakul, M.; Caria, S.; Hinds, M.G. The Bcl-2 Family in Host-Virus Interactions. Viruses 2017, 9, 290.
  10. Kvansakul, M.; Hinds, M.G. The structural biology of BH3-only proteins. Methods Enzymol. 2014, 544, 49–74.
  11. Holm, L.; Laakso, L.M. Dali server update. Nucleic Acids Res. 2016, 44, W351–W355.
  12. Wheeler, T.J.; Clements, J.; Finn, R.D. Skylign: A tool for creating informative, interactive logos representing sequence alignments and profile hidden Markov models. BMC Bioinform. 2014, 15, 7.
  13. Petros, A.M.; Medek, A.; Nettesheim, D.G.; Kim, D.H.; Yoon, H.S.; Swift, K.; Matayoshi, E.D.; Oltersdorf, T.; Fesik, S.W. Solution structure of the antiapoptotic protein bcl-2. Proc. Natl. Acad. Sci. USA 2001, 98, 3012–3017.
  14. Vaux, D.L.; Cory, S.; Adams, J.M. Bcl-2 gene promotes haemopoietic cell survival and cooperates with c-myc to immortalize pre-B cells. Nature 1988, 335, 440–442.
  15. Denisov, A.Y.; Madiraju, M.S.; Chen, G.; Khadir, A.; Beauparlant, P.; Attardo, G.; Shore, G.C.; Gehring, K. Solution structure of human BCL-w: Modulation of ligand binding by the C-terminal helix. J. Biol. Chem. 2003, 278, 21124–21128.
  16. Gibson, L.; Holmgreen, S.P.; Huang, D.C.; Bernard, O.; Copeland, N.G.; Jenkins, N.A.; Sutherland, G.R.; Baker, E.; Adams, J.M.; Cory, S. bcl-w, a novel member of the bcl-2 family, promotes cell survival. Oncogene 1996, 13, 665–675.
  17. Hinds, M.G.; Lackmann, M.; Skea, G.L.; Harrison, P.J.; Huang, D.C.; Day, C.L. The structure of Bcl-w reveals a role for the C-terminal residues in modulating biological activity. EMBO J. 2003, 22, 1497–1507.
  18. Boise, L.H.; Gonzalez-Garcia, M.; Postema, C.E.; Ding, L.; Lindsten, T.; Turka, L.A.; Mao, X.; Nunez, G.; Thompson, C.B. bcl-x, a bcl-2-related gene that functions as a dominant regulator of apoptotic cell death. Cell 1993, 74, 597–608.
  19. Muchmore, S.W.; Sattler, M.; Liang, H.; Meadows, R.P.; Harlan, J.E.; Yoon, H.S.; Nettesheim, D.; Chang, B.S.; Thompson, C.B.; Wong, S.L.; et al. X-ray and NMR structure of human Bcl-xL, an inhibitor of programmed cell death. Nature 1996, 381, 335–341.
  20. Rinkenberger, J.L.; Horning, S.; Klocke, B.; Roth, K.; Korsmeyer, S.J. Mcl-1 deficiency results in peri-implantation embryonic lethality. Genes Dev. 2000, 14, 23–27.
  21. Day, C.L.; Chen, L.; Richardson, S.J.; Harrison, P.J.; Huang, D.C.; Hinds, M.G. Solution structure of prosurvival Mcl-1 and characterization of its binding by proapoptotic BH3-only ligands. J. Biol. Chem. 2005, 280, 4738–4744.
  22. Smits, C.; Czabotar, P.E.; Hinds, M.G.; Day, C.L. Structural plasticity underpins promiscuous binding of the prosurvival protein A1. Structure 2008, 16, 818–829.
  23. Karsan, A.; Yee, E.; Kaushansky, K.; Harlan, J.M. Cloning of human Bcl-2 homologue: Inflammatory cytokines induce human A1 in cultured endothelial cells. Blood 1996, 87, 3089–3096.
  24. Ke, N.; Godzik, A.; Reed, J.C. Bcl-B, a novel Bcl-2 family member that differentially binds and regulates Bax and Bak. J. Biol. Chem. 2001, 276, 12481–12484.
  25. Rautureau, G.J.; Yabal, M.; Yang, H.; Huang, D.C.; Kvansakul, M.; Hinds, M.G. The restricted binding repertoire of Bcl-B leaves Bim as the universal BH3-only prosurvival Bcl-2 protein antagonist. Cell Death Dis. 2012, 3, e443.
  26. Rautureau, G.J.; Day, C.L.; Hinds, M.G. The structure of Boo/Diva reveals a divergent Bcl-2 protein. Proteins 2010, 78, 2181–2186.
  27. Arnaud, E.; Ferri, K.F.; Thibaut, J.; Haftek-Terreau, Z.; Aouacheria, A.; Le Guellec, D.; Lorca, T.; Gillet, G. The zebrafish bcl-2 homologue Nrz controls development during somitogenesis and gastrulation via apoptosis-dependent and -independent mechanisms. Cell Death Differ. 2006, 13, 1128–1137.
  28. Suraweera, C.D.; Caria, S.; Jarva, M.; Hinds, M.G.; Kvansakul, M. A structural investigation of NRZ mediated apoptosis regulation in zebrafish. Cell Death Dis. 2018, 9, 967.
  29. Chittenden, T.; Flemington, C.; Houghton, A.B.; Ebb, R.G.; Gallo, G.J.; Elangovan, B.; Chinnadurai, G.; Lutz, R.J. A conserved domain in Bak, distinct from BH1 and BH2, mediates cell death and protein binding functions. EMBO J. 1995, 14, 5589–5596.
  30. Moldoveanu, T.; Liu, Q.; Tocilj, A.; Watson, M.; Shore, G.; Gehring, K. The X-ray structure of a BAK homodimer reveals an inhibitory zinc binding site. Mol. Cell 2006, 24, 677–688.
  31. Oltvai, Z.N.; Milliman, C.L.; Korsmeyer, S.J. Bcl-2 heterodimerizes in vivo with a conserved homolog, Bax, that accelerates programmed cell death. Cell 1993, 74, 609–619.
  32. Suzuki, M.; Youle, R.J.; Tjandra, N. Structure of Bax: Coregulation of dimer formation and intracellular localization. Cell 2000, 103, 645–654.
  33. Hsu, S.Y.; Kaipia, A.; McGee, E.; Lomeli, M.; Hsueh, A.J. Bok is a pro-apoptotic Bcl-2 protein with restricted expression in reproductive tissues and heterodimerizes with selective anti-apoptotic Bcl-2 family members. Proc. Natl. Acad. Sci. USA 1997, 94, 12401–12406.
  34. Yang, E.; Zha, J.; Jockel, J.; Boise, L.H.; Thompson, C.B.; Korsmeyer, S.J. Bad, a heterodimeric partner for Bcl-XL and Bcl-2, displaces Bax and promotes cell death. Cell 1995, 80, 285–291.
  35. Wang, K.; Yin, X.M.; Chao, D.T.; Milliman, C.L.; Korsmeyer, S.J. BID: A novel BH3 domain-only death agonist. Genes Dev. 1996, 10, 2859–2869.
  36. Han, J.; Sabbatini, P.; White, E. Induction of apoptosis by human Nbk/Bik, a BH3-containing protein that interacts with E1B 19K. Mol. Cell Biol. 1996, 16, 5857–5864.
  37. O’Connor, L.; Strasser, A.; O’Reilly, L.A.; Hausmann, G.; Adams, J.M.; Cory, S.; Huang, D.C. Bim: A novel member of the Bcl-2 family that promotes apoptosis. EMBO J. 1998, 17, 384–395.
  38. Puthalakath, H.; Villunger, A.; O’Reilly, L.A.; Beaumont, J.G.; Coultas, L.; Cheney, R.E.; Huang, D.C.; Strasser, A. Bmf: A proapoptotic BH3-only protein regulated by interaction with the myosin V actin motor complex, activated by anoikis. Science 2001, 293, 1829–1832.
  39. Inohara, N.; Ding, L.; Chen, S.; Nunez, G. harakiri, a novel regulator of cell death, encodes a protein that activates apoptosis and interacts selectively with survival-promoting proteins Bcl-2 and Bcl-X(L). EMBO J. 1997, 16, 1686–1694.
  40. Hijikata, M.; Kato, N.; Sato, T.; Kagami, Y.; Shimotohno, K. Molecular cloning and characterization of a cDNA for a novel phorbol-12-myristate-13-acetate-responsive gene that is highly expressed in an adult T-cell leukemia cell line. J. Virol. 1990, 64, 4632–4639.
  41. Nakano, K.; Vousden, K.H. PUMA, a novel proapoptotic gene, is induced by p53. Mol. Cell 2001, 7, 683–694.
  42. Liang, X.H.; Kleeman, L.K.; Jiang, H.H.; Gordon, G.; Goldman, J.E.; Berry, G.; Herman, B.; Levine, B. Protection against fatal Sindbis virus encephalitis by beclin, a novel Bcl-2-interacting protein. J. Virol. 1998, 72, 8586–8596.
  43. Prudent, J.; Gillet, G.; Popgeorgiev, N. Nrz but not zBcl-xL antagonizes Bcl-wav pro-apoptotic activity in zebrafish. Commun. Integr. Biol. 2014, 7, e28008.
  44. Prudent, J.; Popgeorgiev, N.; Bonneau, B.; Thibaut, J.; Gadet, R.; Lopez, J.; Gonzalo, P.; Rimokh, R.; Manon, S.; Houart, C.; et al. Bcl-wav and the mitochondrial calcium uniporter drive gastrula morphogenesis in zebrafish. Nat. Commun. 2013, 4, 2330.
  45. Quinn, L.; Coombe, M.; Mills, K.; Daish, T.; Colussi, P.; Kumar, S.; Richardson, H. Buffy, a Drosophila Bcl-2 protein, has anti-apoptotic and cell cycle inhibitory functions. EMBO J. 2003, 22, 3568–3579.
  46. Colussi, P.A.; Quinn, L.M.; Huang, D.C.; Coombe, M.; Read, S.H.; Richardson, H.; Kumar, S. Debcl, a proapoptotic Bcl-2 homologue, is a component of the Drosophila melanogaster cell death machinery. J. Cell Biol. 2000, 148, 703–714.
  47. Henderson, S.; Huen, D.; Rowe, M.; Dawson, C.; Johnson, G.; Rickinson, A. Epstein-Barr virus-coded BHRF1 protein, a viral homologue of Bcl-2, protects human B cells from programmed cell death. Proc. Natl. Acad. Sci. USA 1993, 90, 8479–8483.
  48. Huang, Q.; Petros, A.M.; Virgin, H.W.; Fesik, S.W.; Olejniczak, E.T. Solution structure of the BHRF1 protein from Epstein-Barr virus, a homolog of human Bcl-2. J. Mol. Biol. 2003, 332, 1123–1130.
  49. Sarid, R.; Sato, T.; Bohenzky, R.A.; Russo, J.J.; Chang, Y. Kaposi’s sarcoma-associated herpesvirus encodes a functional Bcl-2 homologue. Nat. Med. 1997, 3, 293–298.
  50. White, E.; Sabbatini, P.; Debbas, M.; Wold, W.S.; Kusher, D.I.; Gooding, L.R. The 19-kilodalton adenovirus E1B transforming protein inhibits programmed cell death and prevents cytolysis by tumor necrosis factor alpha. Mol. Cell Biol. 1992, 12, 2570–2580.
  51. Wang, G.H.; Garvey, T.L.; Cohen, J.I. The murine gammaherpesvirus-68 M11 protein inhibits Fas- and TNF-induced apoptosis. J. Gen. Virol. 1999, 80 Pt 10, 2737–2740.
  52. Sinha, S.; Colbert, C.L.; Becker, N.; Wei, Y.; Levine, B. Molecular basis of the regulation of Beclin 1-dependent autophagy by the gamma-herpesvirus 68 Bcl-2 homolog M11. Autophagy 2008, 4, 989–997.
  53. Brun, A.; Rivas, C.; Esteban, M.; Escribano, J.M.; Alonso, C. African swine fever virus gene A179L, a viral homologue of Bcl-2, protects cells from programmed cell death. Virology 1996, 225, 227–230.
  54. Banjara, S.; Caria, S.; Dixon, L.K.; Hinds, M.G.; Kvansakul, M. Structural Insight into African Swine Fever Virus A179L-Mediated Inhibition of Apoptosis. J. Virol. 2017, 91, e02228-16.
  55. Stewart, T.L.; Wasilenko, S.T.; Barry, M. Vaccinia virus F1L protein is a tail-anchored protein that functions at the mitochondria to inhibit apoptosis. J. Virol. 2005, 79, 1084–1098.
  56. Kvansakul, M.; Yang, H.; Fairlie, W.D.; Czabotar, P.E.; Fischer, S.F.; Perugini, M.A.; Huang, D.C.; Colman, P.M. Vaccinia virus anti-apoptotic F1L is a novel Bcl-2-like domain-swapped dimer that binds a highly selective subset of BH3-containing death ligands. Cell Death Differ. 2008, 15, 1564–1571.
  57. Burton, D.R.; Caria, S.; Marshall, B.; Barry, M.; Kvansakul, M. Structural basis of Deerpox virus-mediated inhibition of apoptosis. Acta Crystallogr. D Biol. Crystallogr. 2015, 71, 1593–1603.
  58. Banadyga, L.; Lam, S.C.; Okamoto, T.; Kvansakul, M.; Huang, D.C.; Barry, M. Deerpox virus encodes an inhibitor of apoptosis that regulates Bak and Bax. J. Virol. 2011, 85, 1922–1934.
  59. Opgenorth, A.; Graham, K.; Nation, N.; Strayer, D.; McFadden, G. Deletion analysis of two tandemly arranged virulence genes in myxoma virus, M11L and myxoma growth factor. J. Virol. 1992, 66, 4720–4731.
  60. Kvansakul, M.; van Delft, M.F.; Lee, E.F.; Gulbis, J.M.; Fairlie, W.D.; Huang, D.C.; Colman, P.M. A structural viral mimic of prosurvival Bcl-2: A pivotal role for sequestering proapoptotic Bax and Bak. Mol. Cell 2007, 25, 933–942.
  61. Banadyga, L.; Gerig, J.; Stewart, T.; Barry, M. Fowlpox virus encodes a Bcl-2 homologue that protects cells from apoptotic death through interaction with the proapoptotic protein Bak. J. Virol. 2007, 81, 11032–11045.
  62. Anasir, M.I.; Caria, S.; Skinner, M.A.; Kvansakul, M. Structural basis of apoptosis inhibition by the fowlpox virus protein FPV039. J. Biol. Chem. 2017, 292, 9010–9021.
  63. Tulman, E.R.; Afonso, C.L.; Lu, Z.; Zsak, L.; Kutish, G.F.; Rock, D.L. The genome of canarypox virus. J. Virol. 2004, 78, 353–366.
  64. Anasir, M.I.; Baxter, A.A.; Poon, I.K.H.; Hulett, M.D.; Kvansakul, M. Structural and Functional Insight into Canarypox Virus CNP058 Mediated Regulation of Apoptosis. Viruses 2017, 9, 305.
  65. Okamoto, T.; Campbell, S.; Mehta, N.; Thibault, J.; Colman, P.M.; Barry, M.; Huang, D.C.; Kvansakul, M. Sheeppox Virus SPPV14 Encodes a Bcl-2-like Cell Death Inhibitor that Counters a Distinct Set of Mammalian Pro-apoptotic Proteins. J. Virol. 2012, 15, 11501–11511.
  66. Chathura D. Suraweera; Denis R. Burton; Mark G. Hinds; Marc Kvansakul; Crystal structures of the sheeppox virus encoded inhibitor of apoptosis SPPV14 bound to the proapoptotic BH3 peptides Hrk and Bax. FEBS Letters 2020, 594, 2016-2026, 10.1002/1873-3468.13807.
  67. Chathura D. Suraweera; Mohd Ishtiaq Anasir; Srishti Chugh; Airah Javorsky; Rachael E. Impey; Mohammad Hasan Zadeh; Tatiana P. Soares da Costa; Mark G. Hinds; Marc Kvansakul; Structural insight into tanapoxvirus‐mediated inhibition of apoptosis. The FEBS Journal 2020, 287, 3733-3750, 10.1111/febs.15365.
  68. Westphal, D.; Ledgerwood, E.C.; Tyndall, J.D.; Hibma, M.H.; Ueda, N.; Fleming, S.B.; Mercer, A.A. The orf virus inhibitor of apoptosis functions in a Bcl-2-like manner, binding and neutralizing a set of BH3-only proteins and active Bax. Apoptosis 2009, 14, 1317–1330.
  69. Chathura D. Suraweera; Mark G. Hinds; Marc Kvansakul; Crystal structures of ORFV125 provide insight into orf virus-mediated inhibition of apoptosis. Biochemical Journal 2020, 477, 4527-4541, 10.1042/bcj20200776.
  70. Banjara, S.; Mao, J.; Ryan, T.M.; Caria, S.; Kvansakul, M. Grouper iridovirus GIV66 is a Bcl-2 protein that inhibits apoptosis by exclusively sequestering Bim. J. Biol. Chem. 2018, 293, 5464–5477.
  71. Lin, P.W.; Huang, Y.J.; John, J.A.; Chang, Y.N.; Yuan, C.H.; Chen, W.Y.; Yeh, C.H.; Shen, S.T.; Lin, F.P.; Tsui, W.H.; et al. Iridovirus Bcl-2 protein inhibits apoptosis in the early stage of viral infection. Apoptosis 2008, 13, 165–176.
  72. Bartlett, N.; Symons, J.A.; Tscharke, D.C.; Smith, G.L. The vaccinia virus N1L protein is an intracellular homodimer that promotes virulence. J. Gen. Virol. 2002, 83, 1965–1976.
  73. Cooray, S.; Bahar, M.W.; Abrescia, N.G.; McVey, C.E.; Bartlett, N.W.; Chen, R.A.; Stuart, D.I.; Grimes, J.M.; Smith, G.L. Functional and structural studies of the vaccinia virus virulence factor N1 reveal a Bcl-2-like anti-apoptotic protein. J. Gen. Virol. 2007, 88, 1656–1666.
  74. Fedosyuk, S.; Grishkovskaya, I.; de Almeida Ribeiro, E., Jr.; Skern, T. Characterization and structure of the vaccinia virus NF-kappaB antagonist A46. J. Biol.Chem. 2014, 289, 3749–3762.
  75. Gonzalez, J.M.; Esteban, M. A poxvirus Bcl-2-like gene family involved in regulation of host immune response: Sequence similarity and evolutionary history. Virol. J. 2010, 7, 59.
  76. Neidel, S.; Maluquer de Motes, C.; Mansur, D.S.; Strnadova, P.; Smith, G.L.; Graham, S.C. Vaccinia virus protein A49 is an unexpected member of the B-cell Lymphoma (Bcl)-2 protein family. J. Biol. Chem. 2015, 290, 5991–6002.
  77. Mansur, D.S.; Maluquer de Motes, C.; Unterholzner, L.; Sumner, R.P.; Ferguson, B.J.; Ren, H.; Strnadova, P.; Bowie, A.G.; Smith, G.L. Poxvirus targeting of E3 ligase beta-TrCP by molecular mimicry: A mechanism to inhibit NF-kappaB activation and promote immune evasion and virulence. PLoS Pathog. 2013, 9, e1003183.
  78. Graham, S.C.; Bahar, M.W.; Cooray, S.; Chen, R.A.; Whalen, D.M.; Abrescia, N.G.; Alderton, D.; Owens, R.J.; Stuart, D.I.; Smith, G.L.; et al. Vaccinia virus proteins A52 and B14 Share a Bcl-2-like fold but have evolved to inhibit NF-kappaB rather than apoptosis. PLoS Pathog. 2008, 4, e1000128.
  79. Chen, R.A.; Jacobs, N.; Smith, G.L. Vaccinia virus strain Western Reserve protein B14 is an intracellular virulence factor. J. Gen. Virol. 2006, 87, 1451–1458.
  80. Schroder, M.; Baran, M.; Bowie, A.G. Viral targeting of DEAD box protein 3 reveals its role in TBK1/IKKepsilon-mediated IRF activation. EMBO J. 2008, 27, 2147–2157.
  81. Kalverda, A.P.; Thompson, G.S.; Vogel, A.; Schroder, M.; Bowie, A.G.; Khan, A.R.; Homans, S.W. Poxvirus K7 protein adopts a Bcl-2 fold: Biochemical mapping of its interactions with human DEAD box RNA helicase DDX3. J. Mol. Biol. 2009, 385, 843–853.
  82. Wiens, M.; Belikov, S.I.; Kaluzhnaya, O.V.; Schroder, H.C.; Hamer, B.; Perovic-Ottstadt, S.; Borejko, A.; Luthringer, B.; Muller, I.M.; Muller, W.E. Axial (apical-basal) expression of pro-apoptotic and pro-survival genes in the lake baikal demosponge Lubomirskia baicalensis. DNA Cell Biol. 2006, 25, 152–164.
  83. Wiens, M.; Diehl-Seifert, B.; Muller, W.E. Sponge Bcl-2 homologous protein (BHP2-GC) confers distinct stress resistance to human HEK-293 cells. Cell Death Differ. 2001, 8, 887–898.
  84. Nikolay Popgeorgiev; Jaison D Sa; Lea Jabbour; Suresh Banjara; Trang Thi Minh Nguyen; Aida Akhavan-E-Sabet; Rudy Gadet; Nikola Ralchev; Stéphen Manon; Mark G. Hinds; et al.Hans-Jürgen OsigusBernd SchierwaterPatrick O. HumbertRuth RimokhGermain GilletMarc Kvansakul Ancient and conserved functional interplay between Bcl-2 family proteins in the mitochondrial pathway of apoptosis. Science Advances 2020, 6, eabc4149, 10.1126/sciadv.abc4149.
  85. Suresh Banjara; Jaison D Sa; Mark G. Hinds; Marc Kvansakul; The structural basis of Bcl-2 mediated cell death regulation in hydra. Biochemical Journal 2020, 477, 3287-3297, 10.1042/bcj20200556.
  86. Yan, N.; Gu, L.; Kokel, D.; Chai, J.; Li, W.; Han, A.; Chen, L.; Xue, D.; Shi, Y. Structural, biochemical, and functional analyses of CED-9 recognition by the proapoptotic proteins EGL-1 and CED-4. Mol. Cell 2004, 15, 999–1006.
  87. Conradt, B.; Horvitz, H.R. The C. elegans protein EGL-1 is required for programmed cell death and interacts with the Bcl-2-like protein CED-9. Cell 1998, 93, 519–529.
  88. Hengartner, M.O.; Horvitz, H.R. C. elegans cell survival gene ced-9 encodes a functional homolog of the mammalian proto-oncogene bcl-2. Cell 1994, 76, 665–676.
  89. Woo, J.S.; Jung, J.S.; Ha, N.C.; Shin, J.; Kim, K.H.; Lee, W.; Oh, B.H. Unique structural features of a BCL-2 family protein CED-9 and biophysical characterization of CED-9/EGL-1 interactions. Cell Death Differ. 2003, 10, 1310–1319.
  90. Goldmacher, V.S.; Bartle, L.M.; Skaletskaya, A.; Dionne, C.A.; Kedersha, N.L.; Vater, C.A.; Han, J.W.; Lutz, R.J.; Watanabe, S.; Cahir McFarland, E.D.; et al. A cytomegalovirus-encoded mitochondria-localized inhibitor of apoptosis structurally unrelated to Bcl-2. Proc. Natl. Acad. Sci. USA 1999, 96, 12536–12541.
  91. Ma, J.; Edlich, F.; Bermejo, G.A.; Norris, K.L.; Youle, R.J.; Tjandra, N. Structural mechanism of Bax inhibition by cytomegalovirus protein vMIA. Proc. Natl. Acad. Sci. USA 2012, 109, 20901–20906.
  92. Gavathiotis, E.; Suzuki, M.; Davis, M.L.; Pitter, K.; Bird, G.H.; Katz, S.G.; Tu, H.C.; Kim, H.; Cheng, E.H.; Tjandra, N.; et al. BAX activation is initiated at a novel interaction site. Nature 2008, 455, 1076–1081.
  93. Lalle, P.; Aouacheria, A.; Dumont-Miscopein, A.; Jambon, M.; Venet, S.; Bobichon, H.; Colas, P.; Deleage, G.; Geourjon, C.; Gillet, G. Evidence for crucial electrostatic interactions between Bcl-2 homology domains BH3 and BH4 in the anti-apoptotic Nr-13 protein. Biochem. J. 2002, 368, 213–221.
  94. De Motes, C.M.; Cooray, S.; Ren, H.; Almeida, G.M.F.; McGourty, K.; Bahar, M.W.; Stuart, D.I.; Grimes, J.M.; Graham, S.C.; Smith, G.L. Inhibition of Apoptosis and NF-kB Activation by Vaccinia Protein N1 Occur via Distinct Binding Surfaces and Make Different Contributions to Virulence. PLoS Pathog. 2011, 7, e1002430.
  95. Huang, D.C.; Strasser, A. BH3-Only proteins-essential initiators of apoptotic cell death. Cell 2000, 103, 839–842.
  96. Popgeorgiev, N.; Jabbour, L.; Gillet, G. Subcellular Localization and Dynamics of the Bcl-2 Family of Proteins. Front. Cell Dev. Biol. 2018, 6, 13.
  97. Aouacheria, A.; Brunet, F.; Gouy, M. Phylogenomics of life-or-death switches in multicellular animals: Bcl-2, BH3-Only, and BNip families of apoptotic regulators. Mol. Biol. Evol. 2005, 22, 2395–2416.
  98. Day, C.L.; Smits, C.; Fan, F.C.; Lee, E.F.; Fairlie, W.D.; Hinds, M.G. Structure of the BH3 domains from the p53-inducible BH3-only proteins Noxa and Puma in complex with Mcl-1. J. Mol. Biol. 2008, 380, 958–971.
  99. Bouillet, P.; Strasser, A. BH3-only protein—Sevolutionarily conserved proapoptotic Bcl-2 family members essential for initiating programmed cell death. J. Cell Sci. 2002, 115, 1567–1574.
  100. Huang, K.; O’Neill, K.L.; Li, J.; Zhou, W.; Han, N.; Pang, X.; Wu, W.; Struble, L.; Borgstahl, G.; Liu, Z.; et al. BH3-only proteins target BCL-xL/MCL-1, not BAX/BAK, to initiate apoptosis. Cell Res. 2019.
  101. Metzstein, M.M.; Stanfield, G.M.; Horvitz, H.R. Genetics of programmed cell death in C. elegans: Past, present and future. Trends Genet. 1998, 14, 410–416.
  102. Prudent, J.; Popgeorgiev, N.; Bonneau, B.; Gillet, G. Bcl-2 proteins, cell migration and embryonic development: Lessons from zebrafish. Cell Death Dis. 2015, 6, e1910.
  103. Hardwick, J.M.; Chen, Y.B.; Jonas, E.A. Multipolar functions of BCL-2 proteins link energetics to apoptosis. Trends Cell Biol. 2012, 22, 318–328.
  104. Aouacheria, A.; Baghdiguian, S.; Lamb, H.M.; Huska, J.D.; Pineda, F.J.; Hardwick, J.M. Connecting mitochondrial dynamics and life-or-death events via Bcl-2 family proteins. Neurochem. Int. 2017, 109, 141–161.
  105. Oberstein, A.; Jeffrey, P.D.; Shi, Y. Crystal structure of the Bcl-XL-Beclin 1 peptide complex: Beclin 1 is a novel BH3-only protein. J. Biol. Chem. 2007, 282, 13123–13132.
  106. Ku, B.; Woo, J.S.; Liang, C.; Lee, K.H.; Hong, H.S.; E, X.; Kim, K.S.; Jung, J.U.; Oh, B.H. Structural and biochemical bases for the inhibition of autophagy and apoptosis by viral BCL-2 of murine gamma-herpesvirus 68. PLoS Pathog. 2008, 4, e25.
  107. Lee, E.F.; Perugini, M.A.; Pettikiriarachchi, A.; Evangelista, M.; Keizer, D.W.; Yao, S.; Fairlie, W.D. The BECN1 N-terminal domain is intrinsically disordered. Autophagy 2016, 12, 460–471.
  108. Huang, W.; Choi, W.; Hu, W.; Mi, N.; Guo, Q.; Ma, M.; Liu, M.; Tian, Y.; Lu, P.; Wang, F.L.; et al. Crystal structure and biochemical analyses reveal Beclin 1 as a novel membrane binding protein. Cell Res. 2012, 22, 473–489.
  109. Hanahan, D.; Weinberg, R.A. Hallmarks of cancer: The next generation. Cell 2011, 144, 646–674.
  110. Aktipis, C.A.; Boddy, A.M.; Jansen, G.; Hibner, U.; Hochberg, M.E.; Maley, C.C.; Wilkinson, G.S. Cancer across the tree of life: Cooperation and cheating in multicellularity. Philos. Trans. R. Soc. Lond. B Biol. Sci. 2015, 370.
  111. Domazet-Loso, T.; Klimovich, A.; Anokhin, B.; Anton-Erxleben, F.; Hamm, M.J.; Lange, C.; Bosch, T.C. Naturally occurring tumours in the basal metazoan Hydra. Nat. Commun. 2014, 5, 4222.
  112. Peters, E.C.; Halas, J.C.; McCarty, H.B. Calicoblastic neoplasms in Acropora palmata, with a review of reports on anomalies of growth and form in corals. J. Natl. Cancer Inst. 1986, 76, 895–912.
  113. Hesselman, D.M.; Blake, N.J.; Peters, E.C. Gonadal neoplasms in hard shell clams Mercenaria spp., from the Indian River, Florida: Occurrence, prevalence, and histopathology. J. Invertebr. Pathol. 1988, 52, 436–446.
  114. Albuquerque, T.A.F.; Drummond do Val, L.; Doherty, A.; de Magalhaes, J.P. From humans to hydra: Patterns of cancer across the tree of life. Biol. Rev. Camb. Philos. Soc. 2018, 93, 1715–1734.
  115. Lasi, M.; Pauly, B.; Schmidt, N.; Cikala, M.; Stiening, B.; Kasbauer, T.; Zenner, G.; Popp, T.; Wagner, A.; Knapp, R.T.; et al. The molecular cell death machinery in the simple cnidarian Hydra includes an expanded caspase family and pro- and anti-apoptotic Bcl-2 proteins. Cell Res. 2010, 20, 812–825.
  116. Kvansakul, M.; Hinds, M.G. Structural biology of the Bcl-2 family and its mimicry by viral proteins. Cell Death Dis. 2013, 4, e909.
  117. Chiou, S.K.; Tseng, C.C.; Rao, L.; White, E. Functional complementation of the adenovirus E1B 19-kilodalton protein with Bcl-2 in the inhibition of apoptosis in infected cells. J. Virol. 1994, 68, 6553–6566.
  118. Zhang, T.Y.; Chen, H.Y.; Cao, J.L.; Xiong, H.L.; Mo, X.B.; Li, T.L.; Kang, X.Z.; Zhao, J.H.; Yin, B.; Zhao, X.; et al. Structural and functional analyses of hepatitis B virus X protein BH3-like domain and Bcl-xL interaction. Nat. Commun. 2019, 10, 3192.
  119. Kvansakul, M.; Wei, A.H.; Fletcher, J.I.; Willis, S.N.; Chen, L.; Roberts, A.W.; Huang, D.C.; Colman, P.M. Structural basis for apoptosis inhibition by Epstein-Barr virus BHRF1. PLoS Pathog. 2010, 6, e1001236.
  120. Fitzsimmons, L.; Cartlidge, R.; Chang, C.; Sejic, N.; Galbraith, L.C.A.; Suraweera, C.D.; Croom-Carter, D.; Dewson, G.; Tierney, R.J.; Bell, A.I.; et al. EBV BCL-2 homologue BHRF1 drives chemoresistance and lymphomagenesis by inhibiting multiple cellular pro-apoptotic proteins. Cell Death Differ. 2019.
  121. Desbien, A.L.; Kappler, J.W.; Marrack, P. The Epstein-Barr virus Bcl-2 homolog, BHRF1, blocks apoptosis by binding to a limited amount of Bim. Proc. Natl. Acad. Sci. USA 2009, 106, 5663–5668.
  122. Virgin, H.W.T.; Latreille, P.; Wamsley, P.; Hallsworth, K.; Weck, K.E.; Dal Canto, A.J.; Speck, S.H. Complete sequence and genomic analysis of murine gammaherpesvirus 68. J. Virol. 1997, 71, 5894–5904.
  123. Piya, S.; White, E.J.; Klein, S.R.; Jiang, H.; McDonnell, T.J.; Gomez-Manzano, C.; Fueyo, J. The E1B19K oncoprotein complexes with Beclin 1 to regulate autophagy in adenovirus-infected cells. PLoS ONE 2011, 6, e29467.
  124. Chathura D. Suraweera; Mark G. Hinds; Marc Kvansakul; Poxviral Strategies to Overcome Host Cell Apoptosis. Pathogens 2020, 10, 6, 10.3390/pathogens10010006.
  125. Wasilenko, S.T.; Stewart, T.L.; Meyers, A.F.; Barry, M. Vaccinia virus encodes a previously uncharacterized mitochondrial-associated inhibitor of apoptosis. Proc. Natl. Acad. Sci. USA 2003, 100, 14345–14350.
  126. Fischer, S.F.; Ludwig, H.; Holzapfel, J.; Kvansakul, M.; Chen, L.; Huang, D.C.; Sutter, G.; Knese, M.; Hacker, G. Modified vaccinia virus Ankara protein F1L is a novel BH3-domain-binding protein and acts together with the early viral protein E3L to block virus-associated apoptosis. Cell Death Differ. 2006, 13, 109–118.
  127. Campbell, S.; Thibault, J.; Mehta, N.; Colman, P.M.; Barry, M.; Kvansakul, M. Structural insight into BH3 domain binding of vaccinia virus antiapoptotic F1L. J. Virol. 2014, 88, 8667–8677.
  128. Czabotar, P.E.; Westphal, D.; Dewson, G.; Ma, S.; Hockings, C.; Fairlie, W.D.; Lee, E.F.; Yao, S.; Robin, A.Y.; Smith, B.J.; et al. Bax crystal structures reveal how BH3 domains activate Bax and nucleate its oligomerization to induce apoptosis. Cell 2013, 152, 519–531.
  129. Campbell, S.; Hazes, B.; Kvansakul, M.; Colman, P.; Barry, M. Vaccinia virus F1L interacts with Bak using highly divergent Bcl-2 homology domains and replaces the function of Mcl-1. J. Biol. Chem. 2010, 285, 4695–4708.
  130. Caria, S.; Marshall, B.; Burton, R.L.; Campbell, S.; Pantaki-Eimany, D.; Hawkins, C.J.; Barry, M.; Kvansakul, M. The N Terminus of the Vaccinia Virus Protein F1L Is an Intrinsically Unstructured Region That Is Not Involved in Apoptosis Regulation. J. Biol. Chem. 2016, 291, 14600–14608.
  131. Yu, E.; Zhai, D.; Jin, C.; Gerlic, M.; Reed, J.C.; Liddington, R. Structural determinants of caspase-9 inhibition by the vaccinia virus protein, F1L. J. Biol. Chem. 2011, 286, 30748–30758.
  132. Zhai, D.; Yu, E.; Jin, C.; Welsh, K.; Shiau, C.W.; Chen, L.; Salvesen, G.S.; Liddington, R.; Reed, J.C. Vaccinia virus protein F1L is a caspase-9 inhibitor. J. Biol. Chem. 2010, 285, 5569–5580.
  133. Marshall, B.; Puthalakath, H.; Caria, S.; Chugh, S.; Doerflinger, M.; Colman, P.M.; Kvansakul, M. Variola virus F1L is a Bcl-2-like protein that unlike its vaccinia virus counterpart inhibits apoptosis independent of Bim. Cell Death Dis. 2015, 6, e1680.
  134. Everett, H.; Barry, M.; Lee, S.F.; Sun, X.; Graham, K.; Stone, J.; Bleackley, R.C.; McFadden, G. M11L: A novel mitochondria-localized protein of myxoma virus that blocks apoptosis of infected leukocytes. J. Exp. Med. 2000, 191, 1487–1498.
  135. Douglas, A.E.; Corbett, K.D.; Berger, J.M.; McFadden, G.; Handel, T.M. Structure of M11L: A myxoma virus structural homolog of the apoptosis inhibitor, Bcl-2. Protein Sci. 2007, 16, 695–703.
  136. Neilan, J.G.; Lu, Z.; Afonso, C.L.; Kutish, G.F.; Sussman, M.D.; Rock, D.L. An African swine fever virus gene with similarity to the proto-oncogene bcl-2 and the Epstein-Barr virus gene BHRF1. J. Virol. 1993, 67, 4391–4394.
  137. Banjara, S.; Shimmon, G.L.; Dixon, L.K.; Netherton, C.L.; Hinds, M.G.; Kvansakul, M. Crystal Structure of African Swine Fever Virus A179L with the Autophagy Regulator Beclin. Viruses 2019, 11, 789.
  138. Hernaez, B.; Cabezas, M.; Munoz-Moreno, R.; Galindo, I.; Cuesta-Geijo, M.A.; Alonso, C. A179L, a new viral Bcl2 homolog targeting Beclin 1 autophagy related protein. Curr. Mol. Med. 2013, 13, 305–316.
  139. Aoyagi, M.; Zhai, D.; Jin, C.; Aleshin, A.E.; Stec, B.; Reed, J.C.; Liddington, R.C. Vaccinia virus N1L protein resembles a B cell lymphoma-2 (Bcl-2) family protein. Protein Sci. 2007, 16, 118–124.
  140. Kim, Y.; Lee, H.; Heo, L.; Seok, C.; Choe, J. Structure of vaccinia virus A46, an inhibitor of TLR4 signaling pathway, shows the conformation of VIPER motif. Protein Sci. 2014, 23, 906–914.
  141. Neil D. Young; Tiffany J. Harris; Marco Evangelista; Sharon Tran; Merridee A. Wouters; Tatiana P. Soares Da Costa; Nadia J. Kershaw; Robin B. Gasser; Brian J. Smith; Erinna F. Lee; et al.W. Douglas Fairlie Diversity in the intrinsic apoptosis pathway of nematodes. Communications Biology 2020, 3, 1-12, 10.1038/s42003-020-01208-5.
  142. Simion, P.; Philippe, H.; Baurain, D.; Jager, M.; Richter, D.J.; Di Franco, A.; Roure, B.; Satoh, N.; Queinnec, E.; Ereskovsky, A.; et al. A Large and Consistent Phylogenomic Dataset Supports Sponges as the Sister Group to All Other Animals. Curr. Biol. 2017, 27, 958–967.
  143. Feuda, R.; Dohrmann, M.; Pett, W.; Philippe, H.; Rota-Stabelli, O.; Lartillot, N.; Worheide, G.; Pisani, D. Improved Modeling of Compositional Heterogeneity Supports Sponges as Sister to All Other Animals. Curr. Biol. 2017, 27, 3864–3870.
  144. Srivastava, M.; Simakov, O.; Chapman, J.; Fahey, B.; Gauthier, M.E.; Mitros, T.; Richards, G.S.; Conaco, C.; Dacre, M.; Hellsten, U.; et al. The Amphimedon queenslandica genome and the evolution of animal complexity. Nature 2010, 466, 720–726.
  145. Srivastava, M.; Begovic, E.; Chapman, J.; Putnam, N.H.; Hellsten, U.; Kawashima, T.; Kuo, A.; Mitros, T.; Salamov, A.; Carpenter, M.L.; et al. The Trichoplax genome and the nature of placozoans. Nature 2008, 454, 955–960.
  146. Lasi, M.; David, C.N.; Bottger, A. Apoptosis in pre-Bilaterians: Hydra as a model. Apoptosis 2010, 15, 269–278.
  147. Chapman, J.A.; Kirkness, E.F.; Simakov, O.; Hampson, S.E.; Mitros, T.; Weinmaier, T.; Rattei, T.; Balasubramanian, P.G.; Borman, J.; Busam, D.; et al. The dynamic genome of Hydra. Nature 2010, 464, 592–596.
  148. Aouacheria, A.; Combet, C.; Tompa, P.; Hardwick, J.M. Redefining the BH3 Death Domain as a ‘Short Linear Motif’. Trends Biochem. Sci. 2015, 40, 736–748.
  149. Yan, N.; Chai, J.; Lee, E.S.; Gu, L.; Liu, Q.; He, J.; Wu, J.W.; Kokel, D.; Li, H.; Hao, Q.; et al. Structure of the CED-4-CED-9 complex provides insights into programmed cell death in Caenorhabditis elegans. Nature 2005, 437, 831–837.
  150. Lee, E.F.; Clarke, O.B.; Evangelista, M.; Feng, Z.; Speed, T.P.; Tchoubrieva, E.B.; Strasser, A.; Kalinna, B.H.; Colman, P.M.; Fairlie, W.D. Discovery and molecular characterization of a Bcl-2-regulated cell death pathway in schistosomes. Proc. Natl. Acad. Sci. USA 2011, 108, 6999–7003.
  151. Bender, C.E.; Fitzgerald, P.; Tait, S.W.; Llambi, F.; McStay, G.P.; Tupper, D.O.; Pellettieri, J.; Sanchez Alvarado, A.; Salvesen, G.S.; Green, D.R. Mitochondrial pathway of apoptosis is ancestral in metazoans. Proc. Natl. Acad. Sci. USA 2012, 109, 4904–4909.
  152. Tamura, R.; Takada, M.; Sakaue, M.; Yoshida, A.; Ohi, S.; Hirano, K.; Hayakawa, T.; Hirohashi, N.; Yura, K.; Chiba, K. Starfish Apaf-1 activates effector caspase-3/9 upon apoptosis of aged eggs. Sci. Rep. 2018, 8, 1611.
  153. Eimon, P.M.; Ashkenazi, A. The zebrafish as a model organism for the study of apoptosis. Apoptosis 2010, 15, 331–349.
  154. Kratz, E.; Eimon, P.M.; Mukhyala, K.; Stern, H.; Zha, J.; Strasser, A.; Hart, R.; Ashkenazi, A. Functional characterization of the Bcl-2 gene family in the zebrafish. Cell Death Differ. 2006, 13, 1631–1640.
  155. Glasauer, S.M.; Neuhauss, S.C. Whole-genome duplication in teleost fishes and its evolutionary consequences. Mol. Genet. Genom. 2014, 289, 1045–1060.
  156. Kuwana, T.; Mackey, M.R.; Perkins, G.; Ellisman, M.H.; Latterich, M.; Schneiter, R.; Green, D.R.; Newmeyer, D.D. Bid, Bax, and lipids cooperate to form supramolecular openings in the outer mitochondrial membrane. Cell 2002, 111, 331–342.
  157. Wilfling, F.; Weber, A.; Potthoff, S.; Vogtle, F.N.; Meisinger, C.; Paschen, S.A.; Hacker, G. BH3-only proteins are tail-anchored in the outer mitochondrial membrane and can initiate the activation of Bax. Cell Death Differ. 2012, 19, 1328–1336.
  158. Wilson-Annan, J.; O’Reilly, L.A.; Crawford, S.A.; Hausmann, G.; Beaumont, J.G.; Parma, L.P.; Chen, L.; Lackmann, M.; Lithgow, T.; Hinds, M.G.; et al. Proapoptotic BH3-only proteins trigger membrane integration of prosurvival Bcl-w and neutralize its activity. J. Cell Biol. 2003, 162, 877–887.
  159. Wattenberg, B.W.; Clark, D.; Brock, S. An artificial mitochondrial tail signal/anchor sequence confirms a requirement for moderate hydrophobicity for targeting. Biosci. Rep. 2007, 27, 385–401.
  160. O’Neill, K.L.; Huang, K.; Zhang, J.; Chen, Y.; Luo, X. Inactivation of prosurvival Bcl-2 proteins activates Bax/Bak through the outer mitochondrial membrane. Genes Dev. 2016, 30, 973–988.
  161. Gomez-Fernandez, J.C. Functions of the C-terminal domains of apoptosis-related proteins of the Bcl-2 family. Chem Phys. Lipids 2014, 183, 77–90.
  162. Chin, H.S.; Li, M.X.; Tan, I.K.L.; Ninnis, R.L.; Reljic, B.; Scicluna, K.; Dagley, L.F.; Sandow, J.J.; Kelly, G.L.; Samson, A.L.; et al. VDAC2 enables BAX to mediate apoptosis and limit tumor development. Nat. Commun. 2018, 9, 4976.
  163. Ke, F.F.S.; Vanyai, H.K.; Cowan, A.D.; Delbridge, A.R.D.; Whitehead, L.; Grabow, S.; Czabotar, P.E.; Voss, A.K.; Strasser, A. Embryogenesis and Adult Life in the Absence of Intrinsic Apoptosis Effectors BAX, BAK, and BOK. Cell 2018, 173, 1217–1230.
  164. Zheng, J.H.; Grace, C.R.; Guibao, C.D.; McNamara, D.E.; Llambi, F.; Wang, Y.M.; Chen, T.; Moldoveanu, T. Intrinsic Instability of BOK Enables Membrane Permeabilization in Apoptosis. Cell Rep. 2018, 23, 2083–2094.
  165. Hsu, Y.T.; Youle, R.J. Bax in murine thymus is a soluble monomeric protein that displays differential detergent-induced conformations. J. Biol. Chem. 1998, 273, 10777–10783.
  166. Edlich, F.; Banerjee, S.; Suzuki, M.; Cleland, M.M.; Arnoult, D.; Wang, C.; Neutzner, A.; Tjandra, N.; Youle, R.J. Bcl-x(L) retrotranslocates Bax from the mitochondria into the cytosol. Cell 2011, 145, 104–116.
  167. Wolter, K.G.; Hsu, Y.T.; Smith, C.L.; Nechushtan, A.; Xi, X.G.; Youle, R.J. Movement of Bax from the cytosol to mitochondria during apoptosis. J. Cell Biol. 1997, 139, 1281–1292.
  168. Hsu, Y.T.; Wolter, K.G.; Youle, R.J. Cytosol-to-membrane redistribution of Bax and Bcl-X(L) during apoptosis. Proc. Natl. Acad. Sci. USA 1997, 94, 3668–3672.
  169. Nechushtan, A.; Smith, C.L.; Hsu, Y.T.; Youle, R.J. Conformation of the Bax C-terminus regulates subcellular location and cell death. EMBO J. 1999, 18, 2330–2341.
  170. Echeverry, N.; Bachmann, D.; Ke, F.; Strasser, A.; Simon, H.U.; Kaufmann, T. Intracellular localization of the BCL-2 family member BOK and functional implications. Cell Death Differ. 2013, 20, 785–799.
  171. Todt, F.; Cakir, Z.; Reichenbach, F.; Youle, R.J.; Edlich, F. The C-terminal helix of Bcl-x(L) mediates Bax retrotranslocation from the mitochondria. Cell Death Differ. 2013, 20, 333–342.
  172. Cuconati, A.; White, E. Viral homologs of BCL-2: Role of apoptosis in the regulation of virus infection. Genes Dev. 2002, 16, 2465–2478.
  173. Wang, G.; Barrett, J.W.; Nazarian, S.H.; Everett, H.; Gao, X.; Bleackley, C.; Colwill, K.; Moran, M.F.; McFadden, G. Myxoma virus M11L prevents apoptosis through constitutive interaction with Bak. J. Virol. 2004, 78, 7097–7111.
  174. Poncet, D.; Larochette, N.; Pauleau, A.L.; Boya, P.; Jalil, A.A.; Cartron, P.F.; Vallette, F.; Schnebelen, C.; Bartle, L.M.; Skaletskaya, A.; et al. An anti-apoptotic viral protein that recruits Bax to mitochondria. J. Biol. Chem. 2004, 279, 22605–22614.
  175. Kortschak, R.D.; Samuel, G.; Saint, R.; Miller, D.J. EST analysis of the cnidarian Acropora millepora reveals extensive gene loss and rapid sequence divergence in the model invertebrates. Curr. Biol. 2003, 13, 2190–2195.
  176. Fuchs, Y.; Steller, H. Programmed cell death in animal development and disease. Cell 2011, 147, 742–758.
  177. Clavier, A.; Rincheval-Arnold, A.; Colin, J.; Mignotte, B.; Guenal, I. Apoptosis in Drosophila: Which role for mitochondria? Apoptosis 2016, 21, 239–251.
  178. Doumanis, J.; Dorstyn, L.; Kumar, S. Molecular determinants of the subcellular localization of the Drosophila Bcl-2 homologues DEBCL and BUFFY. Cell Death Differ. 2007, 14, 907–915.
  179. Kroemer, G. Mitochondrial implication in apoptosis. Towards an endosymbiont hypothesis of apoptosis evolution. Cell Death Differ. 1997, 4, 443–456.
More
© Text is available under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/)
ScholarVision Creations
Feedback