Submitted Successfully!
To reward your contribution, here is a gift for you: A free trial for our video production service.
Thank you for your contribution! You can also upload a video entry or images related to this topic.
Version Summary Created by Modification Content Size Created at Operation
1 RBM10 as another p53 activator that can suppress tumor cell growth and proliferation by inducing p53 and its pathway. + 3083 word(s) 3083 2020-09-25 08:58:48 |
2 20201009 format correction -225 word(s) 2858 2020-10-09 03:22:21 |

Video Upload Options

We provide professional Video Production Services to translate complex research into visually appealing presentations. Would you like to try it?

Confirm

Are you sure to Delete?
Cite
If you have any further questions, please contact Encyclopedia Editorial Office.
Jung, J.H.; Lee, H.; Zeng, S.X.; Lu, H. RBM10−a New Regulator of p53. Encyclopedia. Available online: https://encyclopedia.pub/entry/2381 (accessed on 12 December 2024).
Jung JH, Lee H, Zeng SX, Lu H. RBM10−a New Regulator of p53. Encyclopedia. Available at: https://encyclopedia.pub/entry/2381. Accessed December 12, 2024.
Jung, Ji Hoon, Hyemin Lee, Shelya X Zeng, Hua Lu. "RBM10−a New Regulator of p53" Encyclopedia, https://encyclopedia.pub/entry/2381 (accessed December 12, 2024).
Jung, J.H., Lee, H., Zeng, S.X., & Lu, H. (2020, October 07). RBM10−a New Regulator of p53. In Encyclopedia. https://encyclopedia.pub/entry/2381
Jung, Ji Hoon, et al. "RBM10−a New Regulator of p53." Encyclopedia. Web. 07 October, 2020.
RBM10−a New Regulator of p53
Edit

The tumor suppressor p53 acts as a transcription factor that regulates the expression of a number of genes responsible for DNA repair, cell cycle arrest, metabolism, cell migration, angiogenesis, ferroptosis, senescence, and apoptosis. It is the most commonly silenced or mutated gene in cancer, as approximately 50% of all types of human cancers harbor TP53 mutations. Activation of p53 is detrimental to normal cells, thus it is tightly regulated via multiple mechanisms. One of the recently identified regulators of p53 is RNA-binding motif protein 10 (RBM10). RBM10 is an RNA-binding protein frequently deleted or mutated in cancer cells. Its loss of function results in various deformities, such as cleft palate and malformation of the heart, and diseases such as lung adenocarcinoma. In addition, RBM10 mutations are frequently observed in lung adenocarcinomas, colorectal carcinomas, and pancreatic ductal adenocarcinomas. RBM10 plays a regulatory role in alternative splicing. Several recent studies not only linked this splicing regulation of RBM10 to cancer development, but also bridged RBM10′s anticancer function to the p53 pathway.

RBM10 p53 apoptosis MDM2 cancer

1. Introduction 

p53 is one of the best-known tumor suppressors. It is the most popularly researched protein in the field of biomedical sciences, as a continuingly increasing number of research and review articles have been published about p53, in all disciplines of biomedical research, biochemistry, genetics, cellular and molecular biology, pharmacology, clinical research, immunology, and cancer research, since its discovery in 1979 [1][2]. p53 is able to protect normal cells from tumorigenesis in response to a wide range of stimuli, such as ribosomal dysfunction, oxidative stress, DNA damage, lack of nutrients, hypoxia, and oncogenic activation [3][4][5][6]. Once activated, p53 induces apoptosis, ferroptosis, senescence, and cell cycle arrest; and inhibits tumor angiogenesis, cancer cell migration, and metastasis [6][7]. Apoptosis is achieved in part through transcriptional activation of apoptotic genes, which is dependent on offending stressors [8]. Mitochondrial-dependent apoptosis ensures following upregulation of mitochondrial proteins, such as Bax, PUMA, and NOXA [9][10][11]. Furthermore, the autophagy regulator DRAM1 may play a role in p53-dependent apoptosis [12]. Independent of its transcriptional activity, p53 can also function outside of the nucleus, to directly inhibit the activity of anti-apoptotic proteins Bcl-2 and Bcl-xL in the mitochondria [13]. p21, also called WAF1, is an important component of the p53 pathway. Once DNA is damaged, the transcription of p21 is stimulated by p53, resulting in the G1 cell cycle arrest [14][15]. p21 also attenuates EMT (epithelial-mesenchymal transition), a biological process that allows epithelial cells, with loss of cell polarity and cell–cell adhesion via various molecular and biochemical mechanisms, to migrate to distant tissues as mesenchymal cells, by inhibiting the functions of RAS and c-Myc [16]. The importance of p53′s anti-cancer functions in preventing tumor progression is exceedingly highlighted by the high frequency of its functional aberration in human cancers that either harbor mutations in its gene (over 50%) or highly express its oncogenic inhibitor molecules, such as MDM2 or MDMX. Often, mutated p53s, such as hot spot mutants, gain a new oncogenic function [17][18][19][20]. Hence, this p53 pathway is subjected to multi-level regulations.One of the recently identified p53 regulators is RNA-binding motif protein 10 (RBM10; also called S1-1). RBM10 is a member of the RNA binding motif gene family and was first discovered as DXS8237E [21][22] and located on p11.3 of the X chromosome. It has been shown to be involved in pre-mRNA (messenger RNAs) splicing and posttranscriptional regulation [23]. RBM10, a protein with 930 amino acids, contains two RNA recognition motifs (RRM), two zinc fingers, and one G patch motif [24]. RBM10 partially exists in nuclear speckles, and in perichromatin fibrils as the S1-1 granules [25][26], which is correlated with its activity in regulation of gene transcription, mRNA alternative splicing, and stabilization of various genes, including apoptosis related genes [27][28][29][30]. RBM10 has been shown to be a key player in the TARP (Talipes equinovarus, Atrial septal defect, Robin sequence, and Persistent left superior vena cava) syndrome, as its mutations are highly associated with this syndrome [23][31]. This syndrome is a rare condition that affects males (due to one copy X chromosome) and causes several birth defects, such as club foot deformity, congenital heart defects, a smaller jaw, and a retracted or displaced tongue, as reflected in its definition, or name, above. Biochemically, RBM10 has been shown to act as an alternative splicing factor of several pre-mRNAs, such as VEGF [32], Dlg4 [33], FAS, Bcl-x [25], SMN2 [34], and NUMB [35]. RBM10 also possesses splicing-independent functions. For instance, it was shown to mediate an anti-hypertrophy action by associating with Star-PAP (TUT1). This association led to temporary stabilization of angiotensin II type 1 (AT1) receptor mRNA, but reduction of its transcription, consequently inhibiting proliferation, and increasing apoptosis, of vascular smooth muscle cells (VSMC) [36]. RBM10 can also regulate filamin A (FLNa)-binding RhoGTPase-activating protein (FilGAP) activity after translocating from the nucleus into the cellular peripheries by Fyn in response to Src tyrosine kinase signaling [37]. RBM10 has been shown to be involved in potential regulation of transcription of a number of genes [38], though the mechanisms and the importance of these regulations remain to be investigated.

2.  The MDM2-MDMX-p53 Loop

Due to the cytotoxicity of highly active p53, this tumor suppressor needs to be tightly controlled in normal cells. Indeed, unstressed and non-transformed normal cells contain low levels of less potent wild type p53, due to its short half-life [39][40]. This is because a p53 responsive gene encodes a Ring-Finger E3 ubiquitin ligase called MDM2 [41]. Biochemically, MDM2 utilizes at least two mechanisms to inactivate p53. On the one hand, MDM2 binds to the N-terminal domain of p53 and mediates p53 ubiquitination and consequent degradation by the 26 S proteasome [42][43][44]. MDM2 binding to the NH2 terminal transactivation domain of p53 blocks its transcriptional activity via its own N-terminal domain with a hydrophobic pocket. Accordingly, the mutations in the MDM2 binding site of p53 are resistant to proteasomal degradation mediated by MDM2. Similarly, MDM2 mutations that lack p53 binding fail to degrade p53 [45]. MDMX (also called MDM4), an analog of MDM2 [46], further enhances the MDM2 activity to polyubiquitinate p53 by forming a complex with MDM2, through their respective RING domains [44][47][48][49]. Intriguingly, MDMX itself is a substrate of the MDM2 E3 ligase, thus acting as a competitive substrate for polyubiquitination against p53 [47][50][51]. On the other hand, MDM2 and MDMX can also cooperatively and independently suppress p53′s transcriptional activity by binding to the N-terminal transcriptional domain of p53 via their own N-termini [52]. The mutual dependence of MDM2 and MDMX for their p53-inactivating functions, as well as their essential roles in controlling p53 level and activity in vivo, has been demonstrated in several mouse genetic studies [53][54][55][56][57][58]. Therefore, because both MDM2 and MDMX are p53 responsive transcriptional targets, they play essential roles in controlling p53 level and activity in a negative feedback fashion during embryogenesis and organogenesis. In order to activate p53, it is necessary to overcome this negative feedback regulation. Indeed, it has been shown that diverse stress stimuli, including activation of oncogenes, DNA damage by agents or nutrient deprivation, lead to the drastic increase of p53 levels and activity by inhibiting MDM2 or MDMX activity. In general, this is executed through either increasing expression, and posttranslational modifications, of MDM2 or MDMX, or posttranslational modifications of p53 itself, such as phosphorylation, acetylation, and so on. Consequently, active p53 exerts its cellular functions, as highlighted above, primarily by regulating the expression of its target genes [59].

3.  Regulation of the p53-MDM2-MDMX Loop

Over the past decades, a number of proteins have been identified to regulate this MDM2-MDMX-p53 feedback loop upon stresses. For example, in response to DNA damage caused by chemotherapeutic agents, p53 is post-translationally modified, including phosphorylation by various kinases, such as ATM, ATR, DNA-PK, Chk1, Chk, CDK7/Cyc H, and CKII-FACT [60]. DNA damage signals have also been shown to activate p53 by inducing its acetylation, which is mediated by several histone acetyl-transferases (HATs), including p300, CBP, PCAF, TIP60 and so on [61][62][63][64][65][66][67]. Acetylation of p53 not only enhances its transcriptional activity, but also blocks its ubiquitination mediated by MDM2 as both p300/CBP and MDM2 often target a similar set of lysine residues of p53, and thus these two types of posttranslational modifications (PTM) are mutually exclusive [65][68][69][70]. Also, in response to oncogenic challenges, p53 becomes stabilized through the antagonism of the p53–Mdm2 interaction by p14ARF (p19ARF for mouse), whose transcription can be induced via oncogenic signals, such as activation of E2F1 and c-Myc [71][72][73]. In addition, PTMs of MDM2 and MDMX have been shown to play roles in regulation of this MDM2-MDMX-p53 loop. On the one hand, in response to HER-2/neu-PI3K signaling, ATK became active to phosphorylate MDM2 at several serines and render the phosphorylated MDM2 imported to the nucleus, consequently inactivating p53 [74][75][76][77][78]. On the other hand, in response to DNA damage signals, ATM phosphorylates MDM2 at serine 395, suppressing MDM2 activity toward p53 and consequently activating the latter [79]. Thus, this MDM2-p53 pathway is highly regulated via a variety of signaling pathways, as further discussed below and reviewed by others recently [80][81][82][83]. Furthermore, ATM/ATR-Chk2/Chk1 kinase cascades can lead to MDMX phosphorylation at S342, S367, and S402 in response to DNA damage. This phosphorylation, particularly at S342 and S367, results in the binding of MDMX to 14-3-3, and this binding leads to inactivation of MDMX, consequently activating p53 [84][85][86][87]. This pathway was elegantly validated by a genetic study showing that mutations at S341 (equivalent to human S342), S367, and S402 of mouse MDMX (MDMX-3SA) impair the p53 response to DNA damage signals caused by gamma irradiation in mice [88].

4.  Tumor Suppressive Functions of RBM10 in Cancer Cells

RBM10 is a member of the large RNA binding protein family that regulates all aspects of RNA metabolism [38]. Especially, RBM10 has been shown to act as a regulator of alternative splicing [34][89]. A recent study showed that miR-335 modulates Numb alternative splicing via targeting RBM10 in endometrial cancer [90]. In this family, RBM10 shares a highly similar RNA-binding motif and a 30–50% amino acid sequence identity, with two other members, RBM5 and RBM6 [35]. The RBM10 gene was first cloned from human bone marrow in 1995, and later from rat liver in 1996. Its 3.5 kb OFR stems from 24 exons. This X chromosome-linked RBM10 gene encodes a 930 amino acid protein with two RNA recognition motifs (RRM1 and RRM2), two zinc fingers, and one G patch motif [24] (Figure 1). It is widely expressed in a number of types of cells and regulates gene transcription, mRNA alternative splicing, and stabilization of various genes, including the apoptosis related gene [27][28][29]. Its expression and mutations are highly associated with TARP syndrome that causes high lethality to children [23]. It is also associated with spinal muscular atrophy (SMA) [34].

Cells 09 02107 g002 550

Figure 1. Schematic for functional domains of RNA-binding motif protein 10 (RBM10). Numbers indicate the positions of amino acids.

Interestingly, all of the three RBM proteins have been shown to play a potential role in preventing tumorigenesis. For example, RBM5 and RBM6 are frequently deleted in lung cancer and heavy smokers. First of all, RBM5 is downregulated in about 75% of lung cancers as well as prostate and breast cancers [35][91]. Interestingly, overexpression of RBM5 was also reported to play dual functions in breast cancer [35]. Specifically, RBM5 has been shown to regulate alternative splicing of apoptosis related genes, Fas receptor and c-FLIP, resulting in control of programmed cell death [25][27][91]. Recent studies showed that RBM5 is regulated by long noncoding RNAs (lncRNAs) or miRNAs in cancer cells. For instance, the long noncoding RNA AFAP1-AS1 accelerated the proliferation and metastasis of prostate cancer cells by inhibiting RBM5 expression [92]. Additionally, another lncRNA, AB073614, promoted the proliferation and inhibited apoptosis of cervical cancer cells by repressing RBM5 [93]. RBM6 was first identified in small cell lung carcinoma. This gene has been shown to be deleted or disrupted in lung cancers [94]. Furthermore, RBM6 was reported to inhibit invasion and induce apoptosis, consequently suppressing the cancer cell growth and progression in laryngocarcinoma [95]. Together, these lines of evidence suggest that both RBM5 and RBM6 might play a tumor suppressive role in different types of cancers.More recently, RBM10 was reported to inhibit lung cancer cells cell viability and cell cycle progression [96]. This is well in line with the fact that RBM10 mutations are observed in a number of human cancers, such as lung adenocarcinoma [97][98], pancreatic [99][100], colorectal [101], and thyroid [102] cancers. Accordingly, RBM10 is revealed as a cancer-associated gene and listed in the Catalog of Somatic Mutations in Cancer (COSMIC) database [103]. Mechanistically, RBM10 can induce tumor necrosis factor alpha (TNF-α) and apoptosis [104]. Moreover, it has been recently shown to suppress cancer cell proliferation through its function in alternative splicing of oncogenic mRNAs, such as NUMB [90] and VEGFA [32], or by inhibiting RAP1/AKT/CREB signaling [105]. Furthermore, our recent study showed that over expression of RBM10 reduces cancer cell migration and the EMT related gene Vimentin as well [106]. In addition, our latest study linked the anti-cancer role of RBM10 to its regulation of the MDM2-p53 pathway, as further described below. RBM10 can induce apoptosis of cancer cells by activating p53. Altogether, these studies highly suggest that RBM10, similar to RBM5 and RBM6, possesses a tumor suppressive function via different mechanisms.

5. RBM10 is an Activator of p53

As mentioned above, one of the mechanisms underlying the tumor suppressive role of RBM10 is through regulation of the p53-MDM2 feedback loop. Prior to RBM10, several members of the RBM family have been shown to play a role in the p53 pathway [107][108]. For instance, RBM38 was first shown to act as a tumor suppressor by blocking the p53-MDM2 loop in hepatocellular carcinoma [108]. Upregulation of RBM38 induced p53 expression, and decreased MDM2 expression, in human liver cancer cells. However, this regulation was specific to wt p53, as upregulation of RBM38 did not affect the expression of mutant p53 [108]. Another member of this family, RBM24, which shares high similarity with RBM38 in the RRM region, was found to regulate p21 mRNA expression in response to p53 activation, as p53 binds and activates the promoter of the RBM24 gene [107]. By contrast, RBM25, a potential tumor suppressor, was recently found to bind directly to circAMOTL1L, a circular RNA, and induces its biogenesis as a downstream player of p53 in regulation of EMT, as it is a p53 target gene as well, and its disfunction contributes to prostate cancer progression [109]. Similar to these RBM proteins, RBM10 was recently shown by our group to act as tumor suppression. Its tumor suppression role is well supported by bioinformatics data, as the lower expression of RBM10 is correlated with lower survival rate of colorectal cancer patients [6]. It exerts its anti-cancer function through activation of p53. We showed that overexpression of RBM10 induces p53-dependent apoptosis of various cancer cells. Furthermore, we found that the overexpression of RBM10 can reduce MDM2-mediated ubiquitination and degradation of p53. This inhibition must be executed via the direct interaction between RBM10 and MDM2, as both exogenous, and endogenous, RBM10 and MDM2 can be pulled down via co-immunoprecipitation [106]. This was further confirmed by our domain mapping experiments, showing that the RRM1-Zinc Finger (ZnF) and RRM2 region of RBM10 is crucial for MDM2-binding (Figure 1). This region has also been shown to play an important role in the alternative splicing by RNA motifs in introns or exons of its target RNAs [110]. This domain is also crucial for p53 activation, as deletion of the N-terminal RRM1-ZnF domain leads to partial activation of p53 compared to the full-length RBM10 [106]. Supporting this notion, the ability of mutant RBM10 to bind to MDM2 is reduced as measured by co-IP-IB analysis in cancer cells. Surprisingly, this mutant RBM10 was still able to bind to p53. However, RBM10 does not appear to bind to MDMX. These results suggest that the N-terminal domain of RBM10 is required for MDM2 binding and consequent p53 induction. Therefore, our study unveils RBM10 as another regulator of the MDM2-p53 loop and a tumor suppressor that can inhibit cell proliferation and growth in part by blocking this loop and consequently activating p53 (Figure 2).

Cells 09 02107 g003 550

Figure 2. Schematic for RBM10 regulation of the p53-MDM2 loop. Arrow = activation; Bar = inhibition.

6. Conclusions and Questions

In conclusion, our recent study, as described above, revealed RBM10 as another p53 activator that can suppress tumor cell growth and proliferation by inducing p53 and its pathway. This anti-cancer function of RBM10 is implemented in part by blocking MDM2-mediated ubiquitination and degradation of p53 [106], though it has also been shown to suppress tumorigenesis by selectively modifying alternative splicing [32]. However, there are still some remaining questions. For instance, it still remains unknown how RBM10 is activated to work on the MDM2-p53 loop, and by what signal. Would disfunction of the alternative splicing machinery lead to p53 activation by utilizing RBM10? In addition, it remains to be investigated if the regulation of the loop by RBM10 has anything to do with its function in alternative splicing [25][89]. Moreover, since RBM10 is an RNA binding protein, would it be possible for this protein to regulate the turnover or stability of p53 RNAs? Finally, does RBM10 play a role in regulation of the splicing processes for p53 or MDM2 RNAs? Solving these enticing puzzles would lead to a better understanding of molecular insights into this pathway, and offer useful information for future development of cancer therapy by targeting the RBM10-MDM2-p53 pathway.

References

  1. Nguyen, D.; Liao, W.; Zeng, S.X.; Lu, H. Reviving the guardian of the genome: Small molecule activators of p53. Pharmacol. Ther. 2017, 178, 92–108.
  2. Lu, H. Legends of p53: Untold four-decade stories. J. Mol. Cell Biol. 2019, 11, 521–522.
  3. Meek, D.W. Regulation of the p53 response and its relationship to cancer. Biochem. J. 2015, 469, 325–346.
  4. Zhang, Y.; Lu, H. Signaling to p53: Ribosomal proteins find their way. Cancer Cell 2009, 16, 369–377.
  5. Kastenhuber, E.R.; Lowe, S.W. Putting p53 in Context. Cell 2017, 170, 1062–1078.
  6. Jung, J.H.; Lee, H.; Kim, J.H.; Sim, D.Y.; Ahn, H.; Kim, B.; Chang, S.; Kim, S.H. p53-Dependent Apoptotic Effect of Puromycin via Binding of Ribosomal Protein L5 and L11 to MDM2 and its Combination Effect with RITA or Doxorubicin. Cancers 2019, 11, 582.
  7. Vousden, K.H.; Lane, D.P. p53 in health and disease. Nat. Rev. Mol. Cell Biol. 2007, 8, 275–283.
  8. Vousden, K.H.; Prives, C. Blinded by the Light: The Growing Complexity of p53. Cell 2009, 137, 413–431.
  9. Chipuk, J.E.; Kuwana, T.; Bouchier-Hayes, L.; Droin, N.M.; Newmeyer, D.D.; Schuler, M.; Green, D.R. Direct activation of Bax by p53 mediates mitochondrial membrane permeabilization and apoptosis. Science 2004, 303, 1010–1014.
  10. Kiryu-Seo, S.; Hirayama, T.; Kato, R.; Kiyama, H. Noxa is a critical mediator of p53-dependent motor neuron death after nerve injury in adult mouse. J. Neurosci. 2005, 25, 1442–1447.
  11. Leu, J.I.; Dumont, P.; Hafey, M.; Murphy, M.E.; George, D.L. Mitochondrial p53 activates Bak and causes disruption of a Bak-Mcl1 complex. Nat. Cell Biol. 2004, 6, 443–450.
  12. Crighton, D.; Wilkinson, S.; O’Prey, J.; Syed, N.; Smith, P.; Harrison, P.R.; Gasco, M.; Garrone, O.; Crook, T.; Ryan, K.M. DRAM, a p53-induced modulator of autophagy, is critical for apoptosis. Cell 2006, 126, 121–134.
  13. Green, D.R.; Kroemer, G. Cytoplasmic functions of the tumour suppressor p53. Nature 2009, 458, 1127–1130.
  14. el-Deiry, W.S.; Tokino, T.; Velculescu, V.E.; Levy, D.B.; Parsons, R.; Trent, J.M.; Lin, D.; Mercer, W.E.; Kinzler, K.W.; Vogelstein, B. WAF1, a potential mediator of p53 tumor suppression. Cell 1993, 75, 817–825.
  15. Waldman, T.; Kinzler, K.W.; Vogelstein, B. p21 is necessary for the p53-mediated G1 arrest in human cancer cells. Cancer Res. 1995, 55, 5187–5190.
  16. Liu, M.; Casimiro, M.C.; Wang, C.; Shirley, L.A.; Jiao, X.; Katiyar, S.; Ju, X.; Li, Z.; Yu, Z.; Zhou, J.; et al. p21CIP1 attenuates Ras- and c-Myc-dependent breast tumor epithelial mesenchymal transition and cancer stem cell-like gene expression in vivo. Proc. Natl. Acad. Sci. U S A 2009, 106, 19035–19039.
  17. Wu, G.; Wang, F.; Li, K.; Li, S.; Zhao, C.; Fan, C.; Wang, J. Significance of TP53 mutation in bladder cancer disease progression and drug selection. PeerJ 2019, 7, e8261.
  18. Ham, S.W.; Jeon, H.Y.; Jin, X.; Kim, E.J.; Kim, J.K.; Shin, Y.J.; Lee, Y.; Kim, S.H.; Lee, S.Y.; Seo, S.; et al. TP53 gain-of-function mutation promotes inflammation in glioblastoma. Cell Death Differ. 2019, 26, 409–425.
  19. Ganci, F.; Pulito, C.; Valsoni, S.; Sacconi, A.; Turco, C.; Vahabi, M.; Manciocco, V.; Mazza, E.M.C.; Meens, J.; Karamboulas, C.; et al. PI3K Inhibitors Curtail MYC-dependent Mutant p53 Gain-of-function in Head and Neck Squamous Cell Carcinoma. Clin. Cancer Res. 2020, 26, ‏2956–2971.
  20. Liao, P.; Zeng, S.X.; Zhou, X.; Chen, T.; Zhou, F.; Cao, B.; Jung, J.H.; Del Sal, G.; Luo, S.; Lu, H. Mutant p53 Gains Its Function via c-Myc Activation upon CDK4 Phosphorylation at Serine 249 and Consequent PIN1 Binding. Mol. Cell. 2017, 68, 1134–1146.
  21. Coleman, M.P.; Ambrose, H.J.; Carrel, L.; Nemeth, A.H.; Willard, H.F.; Davies, K.E. A novel gene, DXS8237E, lies within 20 kb upstream of UBE1 in Xp11.23 and has a different X inactivation status. Genomics 1996, 31, 135–138.
  22. Timmer, T.; Terpstra, P.; van den Berg, A.; Veldhuis, P.M.; Ter Elst, A.; van der Veen, A.Y.; Kok, K.; Naylor, S.L.; Buys, C.H. An evolutionary rearrangement of the Xp11.3-11.23 region in 3p21.3, a region frequently deleted in a variety of cancers. Genomics 1999, 60, 238–240.
  23. Gripp, K.W.; Hopkins, E.; Johnston, J.J.; Krause, C.; Dobyns, W.B.; Biesecker, L.G. Long-term survival in TARP syndrome and confirmation of RBM10 as the disease-causing gene. Am. J. Med. Genet. A 2011, 155A, 2516–2520.
  24. Wang, Y.; Gogol-Doring, A.; Hu, H.; Frohler, S.; Ma, Y.; Jens, M.; Maaskola, J.; Murakawa, Y.; Quedenau, C.; Landthaler, M.; et al. Integrative analysis revealed the molecular mechanism underlying RBM10-mediated splicing regulation. EMBO Mol. Med. 2013, 5, 1431–1442.
  25. Inoue, A.; Yamamoto, N.; Kimura, M.; Nishio, K.; Yamane, H.; Nakajima, K. RBM10 regulates alternative splicing. FEBS Lett. 2014, 588, 942–947.
  26. Inoue, A.; Tsugawa, K.; Tokunaga, K.; Takahashi, K.P.; Uni, S.; Kimura, M.; Nishio, K.; Yamamoto, N.; Honda, K.; Watanabe, T.; et al. S1-1 nuclear domains: Characterization and dynamics as a function of transcriptional activity. Biol. Cell 2008, 100, 523–535.
  27. Bonnal, S.; Martinez, C.; Forch, P.; Bachi, A.; Wilm, M.; Valcarcel, J. RBM5/Luca-15/H37 regulates Fas alternative splice site pairing after exon definition. Mol. Cell 2008, 32, 81–95.
  28. Loiselle, J.J.; Roy, J.G.; Sutherland, L.C. RBM10 promotes transformation-associated processes in small cell lung cancer and is directly regulated by RBM5. PLoS ONE 2017, 12, e0180258.
  29. Sun, Y.; Bao, Y.; Han, W.; Song, F.; Shen, X.; Zhao, J.; Zuo, J.; Saffen, D.; Chen, W.; Wang, Z.; et al. Autoregulation of RBM10 and cross-regulation of RBM10/RBM5 via alternative splicing-coupled nonsense-mediated decay. Nucleic Acids Res. 2017, 45, 8524–8540.
  30. Mohan, N.; Kumar, V.; Kandala, D.T.; Kartha, C.C.; Laishram, R.S. A Splicing-Independent Function of RBM10 Controls Specific 3’ UTR Processing to Regulate Cardiac Hypertrophy. Cell Rep. 2018, 24, 3539–3553.
  31. Johnston, J.J.; Teer, J.K.; Cherukuri, P.F.; Hansen, N.F.; Loftus, S.K.; Center, N.I.H.I.S.; Chong, K.; Mullikin, J.C.; Biesecker, L.G. Massively parallel sequencing of exons on the X chromosome identifies RBM10 as the gene that causes a syndromic form of cleft palate. Am. J. Hum. Genet. 2010, 86, 743–748.
  32. Dou, X.Q.; Chen, X.J.; Wen, M.X.; Zhang, S.Z.; Zhou, Q.; Zhang, S.Q. Alternative splicing of VEGFA is regulated by RBM10 in endometrial cancer. Kaohsiung J. Med. Sci. 2020, 36, 13–19.
  33. Zheng, S.; Damoiseaux, R.; Chen, L.; Black, D.L. A broadly applicable high-throughput screening strategy identifies new regulators of Dlg4 (Psd-95) alternative splicing. Genome Res. 2013, 23, 998–1007.
  34. Sutherland, L.C.; Thibault, P.; Durand, M.; Lapointe, E.; Knee, J.M.; Beauvais, A.; Kalatskaya, I.; Hunt, S.C.; Loiselle, J.J.; Roy, J.G.; et al. Splicing arrays reveal novel RBM10 targets, including SMN2 pre-mRNA. BMC Mol. Biol. 2017, 18, 19.
  35. Bechara, E.G.; Sebestyen, E.; Bernardis, I.; Eyras, E.; Valcarcel, J. RBM5, 6, and 10 differentially regulate NUMB alternative splicing to control cancer cell proliferation. Mol. Cell 2013, 52, 720–733.
  36. Mueller, C.F.; Berger, A.; Zimmer, S.; Tiyerili, V.; Nickenig, G. The heterogenous nuclear riboprotein S1-1 regulates AT1 receptor gene expression via transcriptional and posttranscriptional mechanisms. Arch. Biochem. Biophys. 2009, 488, 76–82.
  37. Yamada, H.; Tsutsumi, K.; Nakazawa, Y.; Shibagaki, Y.; Hattori, S.; Ohta, Y. Src Family Tyrosine Kinase Signaling Regulates FilGAP through Association with RBM10. PLoS ONE 2016, 11, e0146593.
  38. Loiselle, J.J.; Sutherland, L.C. RBM10: Harmful or helpful-many factors to consider. J. Cell Biochem. 2018, 119, 3809–3818.
  39. Aubrey, B.J.; Kelly, G.L.; Janic, A.; Herold, M.J.; Strasser, A. How does p53 induce apoptosis and how does this relate to p53-mediated tumour suppression? Cell Death Differ. 2018, 25, 104–113.
  40. Rogel, A.; Popliker, M.; Webb, C.G.; Oren, M. p53 cellular tumor antigen: Analysis of mRNA levels in normal adult tissues, embryos, and tumors. Mol. Cell Biol. 1985, 5, 2851–2855.
  41. Manfredi, J.J. The Mdm2-p53 relationship evolves: Mdm2 swings both ways as an oncogene and a tumor suppressor. Genes Dev. 2010, 24, 1580–1589.
  42. Haupt, Y.; Maya, R.; Kazaz, A.; Oren, M. Mdm2 promotes the rapid degradation of p53. Nature 1997, 387, 296–299.
  43. Honda, R.; Tanaka, H.; Yasuda, H. Oncoprotein MDM2 is a ubiquitin ligase E3 for tumor suppressor p53. FEBS Lett. 1997, 420, 25–27.
  44. Fang, S.; Jensen, J.P.; Ludwig, R.L.; Vousden, K.H.; Weissman, A.M. Mdm2 is a RING finger-dependent ubiquitin protein ligase for itself and p53. J. Biol. Chem. 2000, 275, 8945–8951.
  45. Moll, U.M.; Petrenko, O. The MDM2-p53 interaction. Mol. Cancer Res. 2003, 1, 1001–1008.
  46. Bottger, V.; Bottger, A.; Garcia-Echeverria, C.; Ramos, Y.F.; van der Eb, A.J.; Jochemsen, A.G.; Lane, D.P. Comparative study of the p53-mdm2 and p53-MDMX interfaces. Oncogene 1999, 18, 189–199.
  47. Stad, R.; Little, N.A.; Xirodimas, D.P.; Frenk, R.; van der Eb, A.J.; Lane, D.P.; Saville, M.K.; Jochemsen, A.G. Mdmx stabilizes p53 and Mdm2 via two distinct mechanisms. EMBO Rep. 2001, 2, 1029–1034.
  48. Poyurovsky, M.V.; Priest, C.; Kentsis, A.; Borden, K.L.; Pan, Z.Q.; Pavletich, N.; Prives, C. The Mdm2 RING domain C-terminus is required for supramolecular assembly and ubiquitin ligase activity. EMBO J. 2007, 26, 90–101.
  49. Wang, X.; Wang, J.; Jiang, X. MdmX protein is essential for Mdm2 protein-mediated p53 polyubiquitination. J. Biol. Chem. 2011, 286, 23725–23734.
  50. Sharp, D.A.; Kratowicz, S.A.; Sank, M.J.; George, D.L. Stabilization of the MDM2 oncoprotein by interaction with the structurally related MDMX protein. J. Biol. Chem. 1999, 274, 38189–38196.
  51. Jackson, M.W.; Berberich, S.J. MdmX protects p53 from Mdm2-mediated degradation. Mol. Cell Biol. 2000, 20, 1001–1007.
  52. Wade, M.; Li, Y.C.; Wahl, G.M. MDM2, MDMX and p53 in oncogenesis and cancer therapy. Nat. Rev. Cancer 2013, 13, 83–96.
  53. Zhang, Y.; Zeng, S.X.; Hao, Q.; Lu, H. Monitoring p53 by MDM2 and MDMX is required for endocrine pancreas development and function in a spatio-temporal manner. Dev. Biol. 2017, 423, 34–45.
  54. Shadfan, M.; Lopez-Pajares, V.; Yuan, Z.M. MDM2 and MDMX: Alone and together in regulation of p53. Transl Cancer Res. 2012, 1, 88–89.
  55. Tackmann, N.R.; Zhang, Y. Mouse modelling of the MDM2/MDMX-p53 signalling axis. J. Mol. Cell Biol. 2017, 9, 34–44.
  56. Huang, L.; Yan, Z.; Liao, X.; Li, Y.; Yang, J.; Wang, Z.G.; Zuo, Y.; Kawai, H.; Shadfan, M.; Ganapathy, S.; et al. The p53 inhibitors MDM2/MDMX complex is required for control of p53 activity in vivo. Proc. Natl. Acad. Sci. U S A 2011, 108, 12001–12006.
  57. Linke, K.; Mace, P.D.; Smith, C.A.; Vaux, D.L.; Silke, J.; Day, C.L. Structure of the MDM2/MDMX RING domain heterodimer reveals dimerization is required for their ubiquitylation in trans. Cell Death Differ. 2008, 15, 841–848.
  58. Iyappan, S.; Wollscheid, H.P.; Rojas-Fernandez, A.; Marquardt, A.; Tang, H.C.; Singh, R.K.; Scheffner, M. Turning the RING domain protein MdmX into an active ubiquitin-protein ligase. J. Biol. Chem. 2010, 285, 33065–33072.
  59. Yee, K.S.; Vousden, K.H. Complicating the complexity of p53. Carcinogenesis 2005, 26, 1317–1322.
  60. Appella, E.; Anderson, C.W. Post-translational modifications and activation of p53 by genotoxic stresses. Eur. J. Biochem. 2001, 268, 2764–2772.
  61. Liu, Y.; Tavana, O.; Gu, W. p53 modifications: Exquisite decorations of the powerful guardian. J. Mol. Cell Biol. 2019, 11, 564–577.
  62. Brooks, C.L.; Gu, W. The impact of acetylation and deacetylation on the p53 pathway. Protein Cell 2011, 2, 456–462.
  63. Gu, W.; Luo, J.; Brooks, C.L.; Nikolaev, A.Y.; Li, M. Dynamics of the p53 acetylation pathway. Novartis Found. Symp 2004, 259, 197–205.
  64. Gu, W.; Roeder, R.G. Activation of p53 sequence-specific DNA binding by acetylation of the p53 C-terminal domain. Cell 1997, 90, 595–606.
  65. Li, M.; Luo, J.; Brooks, C.L.; Gu, W. Acetylation of p53 inhibits its ubiquitination by Mdm2. J. Biol Chem. 2002, 277, 50607–50611.
  66. Gu, W.; Shi, X.L.; Roeder, R.G. Synergistic activation of transcription by CBP and p53. Nature 1997, 387, 819–823.
  67. Dai, C.; Shi, D.; Gu, W. Negative regulation of the acetyltransferase TIP60-p53 interplay by UHRF1 (ubiquitin-like with PHD and RING finger domains 1). J. Biol. Chem. 2013, 288, 19581–19592.
  68. Kobet, E.; Zeng, X.; Zhu, Y.; Keller, D.; Lu, H. MDM2 inhibits p300-mediated p53 acetylation and activation by forming a ternary complex with the two proteins. Proc Natl. Acad. Sci U S A 2000, 97, 12547–12552.
  69. Li, M.; Chen, D.; Shiloh, A.; Luo, J.; Nikolaev, A.Y.; Qin, J.; Gu, W. Deubiquitination of p53 by HAUSP is an important pathway for p53 stabilization. Nature 2002, 416, 648–653.
  70. Ito, A.; Lai, C.H.; Zhao, X.; Saito, S.; Hamilton, M.H.; Appella, E.; Yao, T.P. p300/CBP-mediated p53 acetylation is commonly induced by p53-activating agents and inhibited by MDM2. EMBO J. 2001, 20, 1331–1340.
  71. Feng, X.H.; Liang, Y.Y.; Liang, M.; Zhai, W.; Lin, X. Direct Interaction of c-Myc with Smad2 and Smad3 to Inhibit TGF-beta-Mediated Induction of the CDK Inhibitor p15(Ink4B). Mol. Cell. 2016, 63, 1089.
  72. Sherr, C.J.; McCormick, F. The RB and p53 pathways in cancer. Cancer Cell 2002, 2, 103–112.
  73. Zhang, Y.; Xiong, Y.; Yarbrough, W.G. ARF promotes MDM2 degradation and stabilizes p53: ARF-INK4a locus deletion impairs both the Rb and p53 tumor suppression pathways. Cell 1998, 92, 725–734.
  74. Zhou, B.P.; Liao, Y.; Xia, W.; Spohn, B.; Lee, M.H.; Hung, M.C. Cytoplasmic localization of p21Cip1/WAF1 by Akt-induced phosphorylation in HER-2/neu-overexpressing cells. Nat. Cell Biol. 2001, 3, 245–252.
  75. Ashcroft, M.; Ludwig, R.L.; Woods, D.B.; Copeland, T.D.; Weber, H.O.; MacRae, E.J.; Vousden, K.H. Phosphorylation of HDM2 by Akt. Oncogene 2002, 21, 1955–1962.
  76. Gottlieb, T.M.; Leal, J.F.; Seger, R.; Taya, Y.; Oren, M. Cross-talk between Akt, p53 and Mdm2: Possible implications for the regulation of apoptosis. Oncogene 2002, 21, 1299–1303.
  77. Ogawara, Y.; Kishishita, S.; Obata, T.; Isazawa, Y.; Suzuki, T.; Tanaka, K.; Masuyama, N.; Gotoh, Y. Akt enhances Mdm2-mediated ubiquitination and degradation of p53. J. Biol Chem. 2002, 277, 21843–21850.
  78. Meek, D.W.; Anderson, C.W. Posttranslational modification of p53: Cooperative integrators of function. Cold Spring Harb Perspect Biol. 2009, 1, a000950.
  79. Maya, R.; Balass, M.; Kim, S.T.; Shkedy, D.; Leal, J.F.; Shifman, O.; Moas, M.; Buschmann, T.; Ronai, Z.; Shiloh, Y.; et al. ATM-dependent phosphorylation of Mdm2 on serine 395: Role in p53 activation by DNA damage. Genes Dev. 2001, 15, 1067–1077.
  80. Qi, S.M.; Cheng, G.; Cheng, X.D.; Xu, Z.; Xu, B.; Zhang, W.D.; Qin, J.J. Targeting USP7-Mediated Deubiquitination of MDM2/MDMX-p53 Pathway for Cancer Therapy: Are We There Yet? Front. Cell Dev. Biol. 2020, 8, 233.
  81. Liu, Y.; Wang, X.; Wang, G.; Yang, Y.; Yuan, Y.; Ouyang, L. The past, present and future of potential small-molecule drugs targeting p53-MDM2/MDMX for cancer therapy. Eur. J. Med. Chem. 2019, 176, 92–104.
  82. Yee-Lin, V.; Pooi-Fong, W.; Soo-Beng, A.K. Nutlin-3, A p53-Mdm2 Antagonist for Nasopharyngeal Carcinoma Treatment. Mini Rev. Med. Chem. 2018, 18, 173–183.
  83. Inoue, K.; Fry, E.A.; Frazier, D.P. Transcription factors that interact with p53 and Mdm2. Int. J. Cancer 2016, 138, 1577–1585.
  84. Okamoto, K.; Kashima, K.; Pereg, Y.; Ishida, M.; Yamazaki, S.; Nota, A.; Teunisse, A.; Migliorini, D.; Kitabayashi, I.; Marine, J.C.; et al. DNA damage-induced phosphorylation of MdmX at serine 367 activates p53 by targeting MdmX for Mdm2-dependent degradation. Mol. Cell Biol. 2005, 25, 9608–9620.
  85. LeBron, C.; Chen, L.; Gilkes, D.M.; Chen, J. Regulation of MDMX nuclear import and degradation by Chk2 and 14-3-3. EMBO J. 2006, 25, 1196–1206.
  86. Pereg, Y.; Lam, S.; Teunisse, A.; Biton, S.; Meulmeester, E.; Mittelman, L.; Buscemi, G.; Okamoto, K.; Taya, Y.; Shiloh, Y.; et al. Differential roles of ATM- and Chk2-mediated phosphorylations of Hdmx in response to DNA damage. Mol. Cell Biol. 2006, 26, 6819–6831.
  87. Jin, J.; Smith, F.D.; Stark, C.; Wells, C.D.; Fawcett, J.P.; Kulkarni, S.; Metalnikov, P.; O’Donnell, P.; Taylor, P.; Taylor, L.; et al. Proteomic, functional, and domain-based analysis of in vivo 14-3-3 binding proteins involved in cytoskeletal regulation and cellular organization. Curr. Biol. 2004, 14, 1436–1450.
  88. Wang, Z.; Sun, Y. Targeting p53 for Novel Anticancer Therapy. Transl Oncol. 2010, 3, 1–12.
  89. Rodor, J.; FitzPatrick, D.R.; Eyras, E.; Caceres, J.F. The RNA-binding landscape of RBM10 and its role in alternative splicing regulation in models of mouse early development. RNA Biol. 2017, 14, 45–57.
  90. Dou, X.Q.; Chen, X.J.; Zhou, Q.; Wen, M.X.; Zhang, S.Z.; Zhang, S.Q. miR-335 modulates Numb alternative splicing via targeting RBM10 in endometrial cancer. Kaohsiung J. Med. Sci. 2020, 36, 171–177.
  91. Sutherland, L.C.; Wang, K.; Robinson, A.G. RBM5 as a putative tumor suppressor gene for lung cancer. J. Thorac. Oncol. 2010, 5, 294–298.
  92. Yang, Z.T.; An, F.; Hu, J.D.; Zhao, W.H. Long noncoding RNA AFAP1-AS1 accelerates the proliferation and metastasis of prostate cancer via inhibiting RBM5 expression. Eur. Rev. Med. Pharmacol Sci. 2019, 23, 3284–3290.
  93. Guo, L.Y.; Qin, C.F.; Zou, H.X.; Song, M.Y.; Gong, M.L.; Chen, C. LncRNA AB073614 promotes the proliferation and inhibits apoptosis of cervical cancer cells by repressing RBM5. Eur. Rev. Med. Pharmacol Sci. 2020, 24, 7201.
  94. Wang, K.; Ubriaco, G.; Sutherland, L.C. RBM6-RBM5 transcription-induced chimeras are differentially expressed in tumours. BMC Genomics 2007, 8, 348.
  95. Wang, Q.; Wang, F.; Zhong, W.; Ling, H.; Wang, J.; Cui, J.; Xie, T.; Wen, S.; Chen, J. RNA-binding protein RBM6 as a tumor suppressor gene represses the growth and progression in laryngocarcinoma. Gene 2019, 697, 26–34.
  96. Sun, X.; Jia, M.; Sun, W.; Feng, L.; Gu, C.; Wu, T. Functional role of RBM10 in lung adenocarcinoma proliferation. Int. J. Oncol 2019, 54, 467–478.
  97. Imielinski, M.; Berger, A.H.; Hammerman, P.S.; Hernandez, B.; Pugh, T.J.; Hodis, E.; Cho, J.; Suh, J.; Capelletti, M.; Sivachenko, A.; et al. Mapping the hallmarks of lung adenocarcinoma with massively parallel sequencing. Cell 2012, 150, 1107–1120.
  98. Vinayanuwattikun, C.; Le Calvez-Kelm, F.; Abedi-Ardekani, B.; Zaridze, D.; Mukeria, A.; Voegele, C.; Vallee, M.; Purnomosari, D.; Forey, N.; Durand, G.; et al. Elucidating Genomic Characteristics of Lung Cancer Progression from In Situ to Invasive Adenocarcinoma. Sci. Rep. 2016, 6, 31628.
  99. Furukawa, T.; Kuboki, Y.; Tanji, E.; Yoshida, S.; Hatori, T.; Yamamoto, M.; Shibata, N.; Shimizu, K.; Kamatani, N.; Shiratori, K. Whole-exome sequencing uncovers frequent GNAS mutations in intraductal papillary mucinous neoplasms of the pancreas. Sci. Rep. 2011, 1, 161.
  100. Witkiewicz, A.K.; McMillan, E.A.; Balaji, U.; Baek, G.; Lin, W.C.; Mansour, J.; Mollaee, M.; Wagner, K.U.; Koduru, P.; Yopp, A.; et al. Whole-exome sequencing of pancreatic cancer defines genetic diversity and therapeutic targets. Nat. Commun. 2015, 6, 6744.
  101. Giannakis, M.; Mu, X.J.; Shukla, S.A.; Qian, Z.R.; Cohen, O.; Nishihara, R.; Bahl, S.; Cao, Y.; Amin-Mansour, A.; Yamauchi, M.; et al. Genomic Correlates of Immune-Cell Infiltrates in Colorectal Carcinoma. Cell Rep. 2016, 17, 1206.
  102. Ibrahimpasic, T.; Xu, B.; Landa, I.; Dogan, S.; Middha, S.; Seshan, V.; Deraje, S.; Carlson, D.L.; Migliacci, J.; Knauf, J.A.; et al. Genomic Alterations in Fatal Forms of Non-Anaplastic Thyroid Cancer: Identification of MED12 and RBM10 as Novel Thyroid Cancer Genes Associated with Tumor Virulence. Clin. Cancer Res. 2017, 23, 5970–5980.
  103. Zhao, J.; Sun, Y.; Huang, Y.; Song, F.; Huang, Z.; Bao, Y.; Zuo, J.; Saffen, D.; Shao, Z.; Liu, W.; et al. Functional analysis reveals that RBM10 mutations contribute to lung adenocarcinoma pathogenesis by deregulating splicing. Sci. Rep. 2017, 7, 40488.
  104. Wang, K.; Bacon, M.L.; Tessier, J.J.; Rintala-Maki, N.D.; Tang, V.; Sutherland, L.C. RBM10 Modulates Apoptosis and Influences TNF-alpha Gene Expression. J. Cell Death 2012, 5, 1–19.
  105. Jin, X.; Di, X.; Wang, R.; Ma, H.; Tian, C.; Zhao, M.; Cong, S.; Liu, J.; Li, R.; Wang, K. RBM10 inhibits cell proliferation of lung adenocarcinoma via RAP1/AKT/CREB signalling pathway. J. Cell Mol. Med. 2019, 23, 3897–3904.
  106. Jung, J.H.; Lee, H.; Cao, B.; Liao, P.; Zeng, S.X.; Lu, H. RNA-binding motif protein 10 induces apoptosis and suppresses proliferation by activating p53. Oncogene 2020, 39, 1031–1040.
  107. Jiang, Y.; Zhang, M.; Qian, Y.; Xu, E.; Zhang, J.; Chen, X. Rbm24, an RNA-binding protein and a target of p53, regulates p21 expression via mRNA stability. J. Biol. Chem. 2014, 289, 3164–3175.
  108. Ye, J.; Liang, R.; Bai, T.; Lin, Y.; Mai, R.; Wei, M.; Ye, X.; Li, L.; Wu, F. RBM38 plays a tumor-suppressor role via stabilizing the p53-mdm2 loop function in hepatocellular carcinoma. J. Exp. Clin. Cancer Res. 2018, 37, 212.
  109. Yang, Z.; Qu, C.B.; Zhang, Y.; Zhang, W.F.; Wang, D.D.; Gao, C.C.; Ma, L.; Chen, J.S.; Liu, K.L.; Zheng, B.; et al. Dysregulation of p53-RBM25-mediated circAMOTL1L biogenesis contributes to prostate cancer progression through the circAMOTL1L-miR-193a-5p-Pcdha pathway. Oncogene 2019, 38, 2516–2532.
  110. Collins, K.M.; Kainov, Y.A.; Christodolou, E.; Ray, D.; Morris, Q.; Hughes, T.; Taylor, I.A.; Makeyev, E.V.; Ramos, A. An RRM-ZnF RNA recognition module targets RBM10 to exonic sequences to promote exon exclusion. Nucleic Acids Res. 2017, 45, 6761–6774.
More
Information
Contributors MDPI registered users' name will be linked to their SciProfiles pages. To register with us, please refer to https://encyclopedia.pub/register : , , ,
View Times: 751
Revisions: 2 times (View History)
Update Date: 09 Oct 2020
1000/1000
ScholarVision Creations