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Funato, N. Craniofacial Phenotypes and Genetics of DiGeorge Syndrome. Encyclopedia. Available online: https://encyclopedia.pub/entry/23098 (accessed on 26 June 2024).
Funato N. Craniofacial Phenotypes and Genetics of DiGeorge Syndrome. Encyclopedia. Available at: https://encyclopedia.pub/entry/23098. Accessed June 26, 2024.
Funato, Noriko. "Craniofacial Phenotypes and Genetics of DiGeorge Syndrome" Encyclopedia, https://encyclopedia.pub/entry/23098 (accessed June 26, 2024).
Funato, N. (2022, May 19). Craniofacial Phenotypes and Genetics of DiGeorge Syndrome. In Encyclopedia. https://encyclopedia.pub/entry/23098
Funato, Noriko. "Craniofacial Phenotypes and Genetics of DiGeorge Syndrome." Encyclopedia. Web. 19 May, 2022.
Craniofacial Phenotypes and Genetics of DiGeorge Syndrome
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This entry is adapted from the peer-reviewed paper 10.3390/jdb10020018

TBX1, located on chromosome 22q11.21, encodes a T-box transcription factor and is a candidate gene for DiGeorge syndrome (DGS) and velocardiofacial syndrome (VCFS). Studies of Tbx1-mutant mice have provided insights into the underlying pathogenesis of DGS/VCFS and the knowledge to diagnose patients with DGS/VCFS. Genes, miRNAs, and epigenetics could change Tbx1 expression. Polymorphisms, variations, and mutations in TBX1 may induce the penetrance and severity of DGS/VCFS-like craniofacial phenotypes. The molecular basis of the variant sequence of TBX1 will further define how TBX1 contributes to the craniofacial and other phenotypes of DGS/VCFS. Since interactions with TBX1 and other molecules in transcriptional complexes or chromatin remodeling are crucial for TBX1 function, identifying and understanding these genetic and epigenetic modifiers individually for each patient may direct therapeutics to minimize the severity.

22q11.2 deletion syndrome DiGeorge syndrome velocardiofacial syndrome cleft palate skull base

1. Introduction

The 22q11.2 deletion syndrome is one of the most common chromosomal microdeletions, affecting approximately 1 in 4000 live births in humans [1]. A 1.5 to 2.5 Mb hemizygous deletion of chromosome 22q11.2 causes DiGeorge syndrome (DGS; OMIM #188400) and velocardiofacial syndrome (VCFS or Shprintzen VCF syndrome; OMIM #192430) [2]. DGS/VCFS appears to be a genomic disorder distinct from 22q11.2 distal deletion syndrome (OMIM #611867). The clinical phenotype of DGS/VCFS is a complex and variable congenital disability, including cardiovascular defects, thymic hypoplasia, parathyroid hypoplasia, and craniofacial malformations [3]. Craniofacial malformations occur in approximately 60% of patients with DGS/VCFS [4].
TBX1, located on chromosome 22q11.21, encodes a T-box transcription factor and is considered a candidate gene for DGS/VCFS since mutations in TBX1 have been found in patients with DGS/VCFS [5]. Heterozygous Tbx1-mutant (Tbx1+/−) mice exhibit DGS/VCFS-related cardiovascular, parathyroid, and thymic phenotypes, suggesting that TBX1 dosage is critical for cardiovascular, parathyroid and thymic development [6][7][8][9]. Tbx1-null mice exhibit the most clinical features of DGS/VCFS, including craniofacial phenotypes, while Tbx1+/− mice exhibit no significant craniofacial phenotypes [6][7][8][9][10].
There have been some excellent reviews on genetics and cardiovascular anomalies of DGS/VCFS [3][11][12][13]. However, information on the craniofacial anomalies of DGS/VCFS is limited. This research focuses on these phenotypes and summarizes the current understanding of the genetic factors that impact DGS/VCFS-related phenotypes. The researchers also review DGS/VCFS mouse models that have been designed to better understand the pathogenic processes of DGS/VCFS.

2. Craniofacial Phenotypes of Patients with DGS/VCFS

Patients with DGS/VCFS manifest craniofacial anomalies involving the cranium, cranial base, jaws, pharyngeal muscles, ear-nose-throat, palate, teeth, and cervical spine (Table 1 and Table 2). Frequently observed craniofacial phenotypes include velopharyngeal insufficiency (27–92%), enamel hypomineralization (39–41%), hearing loss (33–39%), platybasia (50–91%), and cervical spine anomalies (75%) (Table 1). Delayed development of the hyoid bone has also been reported [14][15].
Table 1. Craniofacial anomalies in patients with DGS/VCFS.
Phenotypes Features Frequency
Palatal anomalies Overt cleft palate 7–11%
  Submucous cleft palate 5–23%
  Bifid uvula 5–10%
  Velopharyngeal insufficiency 27–92%
Dental anomalies Tooth agenesis 15%
  Hypoplasia of primary teeth 32%
  Hypoplasia of permanent teeth 10%
  Enamel hypomineralization of primary teeth 39%
  Enamel hypomineralization of permanent teeth 41%
Ear-nose-throat abnormalities Hearing loss 33–39%
  Otitis media with effusion 2%
  Tracheomalacia/laryngomalacia 2%
  Laryngeal web 1%
Ocular abnormalities Hooding of the upper lid 41%
  Ptosis 9%
  Hooding of the lower lid 6%
  Epicanthal folds 3%
  Distichiasis 3%
Cranial base anomalies Platybasia 50–91%
  Basilar impression 3%
Cervical spine anomalies Atlas (C1) anomalies 75%
  Axis (C2) anomalies 59%
  Fusion of C2–C3 34%
Data were summarized from the following references: [16][17][18][19][20].
Table 2. Craniofacial and skeletal phenotypes of DGS/VCFS and Tbx1-null mice.
  DGS/VCFS Tbx1-Null Mice
Cranium Dolichocephaly Small cranium
  Abnormal skull morphology Hypoplastic parietal bone
  Malar flattening Hypoplastic interparietal bone
  Long face Unfused cranial sutures between frontal and parietal bones
    Temporal bone hypoplasia
    Absent zygomatic arch
    Abnormal zygomatic arch morphology
Cranial Base Platybasia Abnormal fusion of the basioccipital and basisphenoid bones
  Basilar impression Abnormal presphenoid bone morphology
    Abnormal basioccipital bone morphology
Palate Cleft palate Cleft palate
  Submucous cleft palate Submucous cleft palate
  Bifid uvula Bifid uvula
  Highly arched palate  
  Velopharyngeal insufficiency  
Mandible Retrognathia Absent mandibular coronoid process
  Short mandible Short mandible
  Micrognathia Micrognathia
Teeth Enamel hypoplasia Abnormal upper incisor morphology
  Single central incisor Absent upper incisors
  Small teeth  
  Abnormality of the dentition  
  Carious teeth  
Muscles Pharyngeal hypotonia Absent masseter muscle
    Absent pterygoid muscle
    Absent temporalis muscle
Eyes Hypertelorism/telecanthus Hypertelorism
  Downslanted palpebral fissures  
  Proptosis  
  Strabismus  
  Abnormal eyelid morphology  
  Epicanthus  
  Microphthalmia  
External Ears Small earlobe Ear lobe hypoplasia
  Low-set ears Lowered ear position
  Abnormally folded pinna Abnormal ear shape
  Preauricular pit Absent outer ear
    Anotia
Middle and Inner Ears Chronic otitis media Abnormal middle ear ossicle morphology
  Conductive hearing loss Absent middle ear ossicles
  Sensorineural hearing loss Abnormal stapes morphology
  Auditory canal stenosis Abnormal incus morphology
  Pulsatile tympanic membrane Abnormal malleus morphology
  Thickened tympanic membrane Absent stapes
  Tympanic membrane retraction Abnormal external auditory canal morphology
    Decreased tympanic ring size
Nose Prominent nasal bridge Short snout
  Abnormal nasal morphology  
  Underdeveloped nasal alae  
  Choanal atresia  
Throat Abnormal thorax morphology Small thyroid cartilage
  Abnormality of the pharynx Small cricoid cartilage
    Abnormal thyroid cartilage morphology
    Pharynx hypoplasia
Hyoid bones Delayed development of the hyoid bone Hyoid bone hypoplasia
  Invisible hyoid ossification center Abnormal hyoid bone morphology
Cervical spine Dysmorphic C1 Abnormal cervical atlas (C1) morphology
  Anterior arch cleft of C1 Absent arcus anterior of C1
  Open posterior arch C1  
  Fusion of C1–C2  
  Fusion of C2–C3  
  Upswept C2 lamina  
  Platyspondyly  
Others   Short clavicle
References [14][15][16][17][18][19][20][21][22][23][24][25][26] [6][7][8][9][10][27][28][29][30][31][32][33][34]
Data were summarized from the following references [6][7][8][9][10][14][15][16][17][18][19][20][21][22][23][24][25][26][27][28][29][30][31][32][33][34], OMIM (https://www.omim.org accessed on 3 August 2021) and the Monarch Initiative (https://monarchinitiative.org accessed on 3 August 2021).
In addition to morphological anomalies, infants and young children with DGS/VCFS often exhibit a high prevalence of functional difficulties in feeding and speech/language associated with cleft palate, laryngeal anomalies, and velopharyngeal dysfunction [35]. Even after cleft palate closure, children with DGS/VCFS sometimes present communication disorders related to speech-language problems, such as articulation disorders of speech sounds and vocal disorders [35]. They exhibit slower language acquisition than those with other disorders that may be associated with abnormal muscle development.

3. Genetics of DGS/VCFS

DGS/VCFS is caused by a 1.5 to 2.5 Mb hemizygous deletion of chromosome 22q11.2 (Figure 1). Chromosomal microdeletions at 10p14-p13 (the DGS2 locus) in patients with DGS/VCFS phenotypes are defined as the DGS/VCFS complex 2. The researchers here focus on the 22q11.2 locus, its associated genes, and miRNAs.
/media/item_content/202205/6286e85102fb0jdb-10-00018-g001.png
Figure 1. Proximal deletions of chromosome 22q11.2 are responsible for the clinical features of DGS/VCFS. Snapshot of the UCSC Genome Browser (http://genome.ucsc.edu accessed on 3 August 2021) in the hg38 assembly showing the genomic context in the proximal deletions of chromosome 22q11.2. Top, the 25 kb resolution Hi-C data in H1 human embryonic stem cell line (H1-hESC). Bottom, the coding (blue) and noncoding RNAs (green), including miRNAs and long noncoding RNAs, are shown.
Most of the chromosomal deletions of the 22q11.2 locus are de novo, but inherited deletions of the 22q11.2 locus have been reported in 6–28% of patients as autosomal dominant . The majority of clinical phenotypes of DGS/VCFS are caused by proximal 1.5 Mb microdeletions [3][20], resulting in a hemizygosity of approximately 30 coding genes, including DGCR6, PRODH, DGCR2, ESS2, TSSK2, GSC2, FAM246C, SLC25A1, CLTCL1, UFD1, HIRA, CDC45, MRPL40, C22orf39, CLDN5, TBX1, SEPTIN5, SEPT5-GP1BB, GP1BB, GNB1L, RTL10, TXNRD2, COMT, ARVCF, TANGO2, TRMT2A, RANBP1, CCDC188, DGCR8, ZDHHC8, RTN4R, DGCR6L, and C007326, as well as microRNAs (miRNAs) and long noncoding RNAs (Figure 1). The Hi-C chromatin structure of the 1.5 Mb region indicates interactions between these loci and their neighboring regions (Figure 1).

3.1. TBX1 Gene

The proximal deletion of 1.5 Mb on the 22q11.2 locus includes TBX1 (Figure 1). TBX1 is considered a candidate gene of DGS/VCFS because haploinsufficiency of TBX1 leads to the typical phenotypes of DGS/VCFS, conotruncal anomaly face syndrome (OMIM #217095), and tetralogy of Fallot (OMIM #187500) (Table 3). Identical mutations in TBX1 present among patients resulted in distinct phenotypes, suggesting that genetic and epigenetic changes or environmental factors are involved in the clinical phenotypes [5]. Further investigation is required to confirm that the variants cause DGS/VCFS and how they impact the phenotypes.
Table 3. DGS/VCFS-associated variants of TBX1.
Mutation Domain Condition Craniofacial Anomalies References
c.89_284del N-terminal DiGeorge syndrome Yes ClinVar Variant: 971780
c.199_224del N-terminal DiGeorge syndrome Yes ClinVar Variant: 949172
c.292A>T N-terminal DiGeorge syndrome Yes ClinVar Variant: 526036
c.385G>A T-box Tetralogy of Fallot No ClinVar Variant: 488618
c.443T>A (F148Y) T-box Conotruncal anomaly face syndrome Yes [5]
c.503T>C T-box DiGeorge syndrome
Velocardiofacial syndrome
(Shprintzen syndrome)
Tetralogy of Fallot		 Yes ClinVar Variant: 973222
c.569C > A (P190Q) T-box Congenital heart defects No [36]
c.582C>G (H194Q) T-box Velocardiofacial syndrome Yes [37]
c.928G>A (G310S) C-terminal DiGeorge syndrome Yes [5]
c.967_977dup AACCCCGTGGC C-terminal Thymic hypoplasia
Postaxial polydactyly of the right fifth toe		 No [38]
c.1158_1159delinsT C-terminal Hypoparathyroidism and hypocalcemia
Facial asymmetry
Deafness		 Yes [39]
c.1223delC C-terminal Conotruncal anomaly face syndrome
Velocardiofacial syndrome		 Yes [5]
c.1253delA C-terminal DiGeorge syndrome Yes [40]
c.1320-1342del23bp C-terminal Velocardiofacial syndrome Yes/No [41]
c.1399-1428dup30 C-terminal Tetralogy of Fallot
Scoliosis
Facial asymmetry
Upslanting palpebral fissures
Absent pulmonary valve
Isolated left pulmonary artery		 Yes [42]
ClinVar (https://www.ncbi.nlm.nih.gov/clinvar accessed on 3 August 2021).

3.2. DiGeorge Syndrome Critical Region (DGCR)

DGCR8, DGCR6, and DGCR6L map to the commonly deleted 1.5 Mb region in DGS/VCFS (Figure 1). DGCR8 is a nuclear miRNA-binding protein required for miRNA biogenesis. Dgcr8 haploinsufficiency in mice reduces the expression of miRNAs in the brain [43]. DGCR6 and DGCR6L genes encode a protein with a sequence similar to the Drosophila gonadal [44]. In a chicken model, targeting DGCR6 function resulted in a vascular phenotype [45]. Attenuation of DGCR6 affects the expression of three genes localized within the 1.5 Mb region, upregulating the expression of TBX1 and UFD1 and reducing the expression of HIRA in the heart and pharyngeal arches of the chicken embryos [45]. Thus, the haploinsufficiency of DGCR8 or DGCR6 may be linked to DGS/VCFS phenotypes when targeting DGS/VCFS-related genes and miRNAs.

3.3. MicroRNAs

The deleted 1.5 Mb on the 22q11.2 locus includes several miRNAs, such as miR-185, miR-4716, miR-3618, miR-1286, miR-1306, and miR-6816 (Figure 1). The TargetScan miRNA target prediction program (http://www.targetscan.org accessed on 3 August 2021) identified that the 3′ UTR of TBX1 includes conserved sites for miR-183-5p, miR-96-5p, miR-1271-5p, miR-182-5p, miR-144-3p, miR-139-5p, miR-101-3p, and miR-451. Two miRNAs were confirmed to target the 3′ UTR of TBX1. miR-96-5p represses Tbx1 expression and, in turn, TBX1 suppresses the promoter activity and expression of miR-96 [46]. miR-451a, a tumor suppressor, also directly targets TBX1 [47]. The expression of this gene is upregulated in cutaneous basal cell carcinoma, inversely to miR-451a [47]. miR-17-92 fine-tunes the expression of Tbx1 in craniofacial development, suggesting miR-17-92 as a candidate genetic modifier for Tbx1 [48]. Thus, miRNAs both inside and outside the 22q11.2 locus may influence the severity of the clinical phenotypes of DGS/VCFS.

4. Craniofacial Phenotypes of DGS/VCFS Mouse Models

Mouse models with DGS/VCFS help identify additional candidate genes or modifier genes that influence the penetrance and/or severity of DGS/VCFS-related phenotypes. According to the mouse genome informatics (MGI) database (http://www.informatics.jax.org accessed on 3 August 2021), DGS/VCFS-related anomalies concerning Tbx1, Chrd, Tgfbr2, Vegfa, Fgf8, Crkl, Aldh1a2/Raldh2, Hoxa3, Kat6a/Moz/Myst3, Dicer1, Plxnd1, Dock1, Ndst1, Prickle1, Trappc10, Zfp366, and Foxn1 have been reported in genetically altered mice (Table 4). When these genes were analyzed according to biological process, “heart morphogenesis” and “cranial skeletal system development” were enriched. Our enrichment analysis using ToppCluster [49] indicated that genes associated with DGS/VCFS phenotypes in mice are specifically enriched in the morphogenesis of craniofacial tissues and heart (Figure 2A). Interestingly, among these genes, only Tbx1 and Chrd were specifically enriched in the morphogenesis of cricoid and thyroid cartilages (Figure 2A). Genes associated with DGS/VCFS phenotypes in mice also indicated that DGS/VCFS-related phenotypes involve the interaction of several signaling pathways, including bone morphogenetic protein (BMP), transforming growth factor (TGF)β, vascular endothelial growth factor (VEGF), fibroblast growth factor (FGF), and retinoic acid signaling pathways (Figure 2B). Genes involved in the genetic pathway of Tbx1 are likely to induce phenotypes similar to Tbx1-null mice (Figure 2B, Table 4). These are described below.
/media/item_content/202205/62904960e3a44jdb-10-00018-g002.png
Figure 2. Interaction network of genes associated with DGS/VCFS phenotypes in mice. (A) A gene-based network where each gene connects to a feature. The network was constructed using ToppCluster (https://toppcluster.cchmc.org/ accessed on 6 May 2022). Mouse phenotypes are shown in the network. (B) The protein–protein interaction network was constructed using the STRING tool (https://string-db.org/ accessed on 6 May 2022). Genes associated with DGS/VCFS phenotypes in mice (Table 4) were the input. Different colors represent different types of evidence of a connection between proteins.
Table 4. Craniofacial phenotypes of DGS/VCFS mouse model.
Gene Symbol Induced Mutation Type Cranium Palate Teeth Muscles Ear-Nose-Throat Hyoid Bones Cardio-Vascular
Tbx1 Null Yes Yes Yes Yes Yes Yes Yes
Chrd Null Yes Yes nr nr Yes Yes Yes
Tgfbr2 Deletion (Wnt1-Cre) Yes Yes nr nr nr nr Yes
Vegfa Null Yes Yes Yes nr nr nr Yes
Fgf8 Hypomorphic allele Yes Yes Yes nr Yes Yes Yes
Crkl Null Yes nr nr nr Yes nr Yes
Aldh1a2 Hypomorphic allele nr nr nr nr Yes Yes Yes
Hoxa3 Null nr Yes nr Yes Yes Yes Yes
Kat6a Null nr Yes nr nr Yes nr Yes
Dicer1 Deletion (Wnt1-Cre) Yes nr nr nr nr nr Yes
Plxnd1 Single point mutation nr Yes nr nr Yes nr Yes
Dock1 Undefined nr nr nr nr Yes nr Yes
Ndst1 Single point mutation nr nr nr nr Yes nr Yes
Prickle1 Single point mutation Yes Yes nr nr Yes nr Yes
Trappc10 Undefined Yes Yes nr nr nr nr Yes
Zfp366 Single point mutation nr nr nr nr Yes nr Yes
Foxn1 Intragenic deletion nr nr nr nr Yes nr Yes
Mouse models of DiGeorge syndrome with phenotypic similarity to human diseases can be found in the Mouse Genome Informatics (MGI) database (http://www.informatics.jax.org accessed on 3 August 2021). Data were summarized from the following references [6][7][8][9][10][29][30][31][32][33][34][35][36][50][51][52][53][54][55][56][57][58][59]. nr, not reported.

References

  1. Kaimal, V.; Bardes, E.E.; Tabar, S.C.; Jegga, A.G.; Aronow, B.J. ToppCluster: A multiple gene list feature analyzer for comparative enrichment clustering and network-based dissection of biological systems. Nucleic Acids Res. 2010, 38, W96-102.
  2. Jerome, L.A.; Papaioannou, V.E. DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1. Nat. Genet. 2001, 27, 286–291.
  3. Lindsay, E.A.; Vitelli, F.; Su, H.; Morishima, M.; Huynh, T.; Pramparo, T.; Jurecic, V.; Ogunrinu, G.; Sutherland, H.F.; Scambler, P.J.; et al. Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice. Nature 2001, 410, 97–101.
  4. Merscher, S.; Funke, B.; Epstein, J.A.; Heyer, J.; Puech, A.; Lu, M.M.; Xavier, R.J.; Demay, M.B.; Russell, R.G.; Factor, S.; et al. TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge syndrome. Cell 2001, 104, 619–629.
  5. Hu, T.; Yamagishi, H.; Maeda, J.; McAnally, J.; Yamagishi, C.; Srivastava, D. Tbx1 regulates fibroblast growth factors in the anterior heart field through a reinforcing autoregulatory loop involving forkhead transcription factors. Development 2004, 131, 5491–5502.
  6. Liao, J.; Kochilas, L.; Nowotschin, S.; Arnold, J.S.; Aggarwal, V.S.; Epstein, J.A.; Brown, M.C.; Adams, J.; Morrow, B.E. Full spectrum of malformations in velo-cardio-facial syndrome/DiGeorge syndrome mouse models by altering Tbx1 dosage. Hum. Mol. Genet. 2004, 13, 1577–1585.
  7. Zhang, Z.; Huynh, T.; Baldini, A. Mesodermal expression of Tbx1 is necessary and sufficient for pharyngeal arch and cardiac outflow tract development. Development 2006, 133, 3587–3595.
  8. Arnold, J.S.; Werling, U.; Braunstein, E.M.; Liao, J.; Nowotschin, S.; Edelmann, W.; Hebert, J.M.; Morrow, B.E. Inactivation of Tbx1 in the pharyngeal endoderm results in 22q11DS malformations. Development 2006, 133, 977–987.
  9. Arnold, J.S.; Braunstein, E.M.; Ohyama, T.; Groves, A.K.; Adams, J.C.; Brown, M.C.; Morrow, B.E. Tissue-specific roles of Tbx1 in the development of the outer, middle and inner ear, defective in 22q11DS patients. Hum. Mol. Genet. 2006, 15, 1629–1639.
  10. Choi, M.; Klingensmith, J. Chordin is a modifier of tbx1 for the craniofacial malformations of 22q11 deletion syndrome phenotypes in mouse. PLoS Genet. 2009, 5, e1000395.
  11. Moraes, F.; Novoa, A.; Jerome-Majewska, L.A.; Papaioannou, V.E.; Mallo, M. Tbx1 is required for proper neural crest migration and to stabilize spatial patterns during middle and inner ear development. Mech. Dev. 2005, 122, 199–212.
  12. Funato, N.; Nakamura, M.; Richardson, J.A.; Srivastava, D.; Yanagisawa, H. Tbx1 regulates oral epithelial adhesion and palatal development. Hum. Mol. Genet. 2012, 21, 2524–2537.
  13. Funato, N.; Nakamura, M.; Richardson, J.A.; Srivastava, D.; Yanagisawa, H. Loss of Tbx1 induces bone phenotypes similar to cleidocranial dysplasia. Hum. Mol. Genet. 2015, 24, 424–435.
  14. Funato, N.; Srivastava, D.; Shibata, S.; Yanagisawa, H. TBX1 Regulates Chondrocyte Maturation in the Spheno-occipital Synchondrosis. J. Dent. Res. 2020, 99, 1182–1191.
  15. Bachiller, D.; Klingensmith, J.; Shneyder, N.; Tran, U.; Anderson, R.; Rossant, J.; De Robertis, E.M. The role of chordin/Bmp signals in mammalian pharyngeal development and DiGeorge syndrome. Development 2003, 130, 3567–3578.
  16. Wurdak, H.; Ittner, L.M.; Lang, K.S.; Leveen, P.; Suter, U.; Fischer, J.A.; Karlsson, S.; Born, W.; Sommer, L. Inactivation of TGFβ signaling in neural crest stem cells leads to multiple defects reminiscent of DiGeorge syndrome. Genes Dev. 2005, 19, 530–535.
  17. Stalmans, I.; Lambrechts, D.; De Smet, F.; Jansen, S.; Wang, J.; Maity, S.; Kneer, P.; von der Ohe, M.; Swillen, A.; Maes, C.; et al. VEGF: A modifier of the del22q11 (DiGeorge) syndrome? Nat. Med. 2003, 9, 173–182.
  18. Abu-Issa, R.; Smyth, G.; Smoak, I.; Yamamura, K.; Meyers, E.N. Fgf8 is required for pharyngeal arch and cardiovascular development in the mouse. Development 2002, 129, 4613–4625.
  19. Guris, D.L.; Fantes, J.; Tara, D.; Druker, B.J.; Imamoto, A. Mice lacking the homologue of the human 22q11.2 gene CRLK phenocopy neurocristopathies of DiGeorge syndrome. Nat. Genet. 2001, 27, 293–298.
  20. Vermot, J.; Niederreither, K.; Garnier, J.M.; Chambon, P.; Dollé, P. Decreased embryonic retinoic acid synthesis results in a DiGeorge syndrome phenotype in newborn mice. Proc. Natl. Acad. Sci. USA 2003, 100, 1763–1768.
  21. Chisaka, O.; Capecchi, M.R. Regionally restricted developmental defects resulting from targeted disruption of the mouse homeobox gene hox-1.5. Nature 1991, 350, 473–479.
  22. Voss, A.K.; Vanyai, H.K.; Collin, C.; Dixon, M.P.; McLennan, T.J.; Sheikh, B.N.; Scambler, P.; Thomas, T. MOZ Regulates the Tbx1 Locus, and Moz Mutation Partially Phenocopies DiGeorge Syndrome. Dev. Cell 2012, 23, 652–663.
  23. Sheehy, N.T.; Cordes, K.R.; White, M.P.; Ivey, K.N.; Srivastava, D. The neural crest-enriched microRNA miR-452 regulates epithelial-mesenchymal signaling in the first pharyngeal arch. Development 2010, 137, 4307–4316.
  24. Gershwin, M.E. DiGeorge syndrome: Congenital thymic hypoplasia. Animal model: Congenitally athymic (nude) mouse. Am. J. Pathol. 1977, 89, 809–812.
  25. Kobrynski, L.J.; Sullivan, K.E. Velocardiofacial syndrome, DiGeorge syndrome: The chromosome 22q11.2 deletion syndromes. Lancet 2007, 370, 1443–1452.
  26. Oberoi, S.; Vargervik, K. Velocardiofacial syndrome with single central incisor. Am. J. Med. Genet. A 2005, 132A, 194–197.
  27. Zhang, Z.; Huynh, T.; Baldini, A. Mesodermal expression of Tbx1 is necessary and sufficient for pharyngeal arch and cardiac outflow tract development. Development 2006, 133, 3587–3595.
  28. Arnold, J.S.; Werling, U.; Braunstein, E.M.; Liao, J.; Nowotschin, S.; Edelmann, W.; Hebert, J.M.; Morrow, B.E. Inactivation of Tbx1 in the pharyngeal endoderm results in 22q11DS malformations. Development 2006, 133, 977–987.
  29. Arnold, J.S.; Braunstein, E.M.; Ohyama, T.; Groves, A.K.; Adams, J.C.; Brown, M.C.; Morrow, B.E. Tissue-specific roles of Tbx1 in the development of the outer, middle and inner ear, defective in 22q11DS patients. Hum. Mol. Genet. 2006, 15, 1629–1639.
  30. Choi, M.; Klingensmith, J. Chordin is a modifier of tbx1 for the craniofacial malformations of 22q11 deletion syndrome phenotypes in mouse. PLoS Genet. 2009, 5, e1000395.
  31. Moraes, F.; Novoa, A.; Jerome-Majewska, L.A.; Papaioannou, V.E.; Mallo, M. Tbx1 is required for proper neural crest migration and to stabilize spatial patterns during middle and inner ear development. Mech. Dev. 2005, 122, 199–212.
  32. Funato, N.; Nakamura, M.; Richardson, J.A.; Srivastava, D.; Yanagisawa, H. Tbx1 regulates oral epithelial adhesion and palatal development. Hum. Mol. Genet. 2012, 21, 2524–2537.
  33. Funato, N.; Nakamura, M.; Richardson, J.A.; Srivastava, D.; Yanagisawa, H. Loss of Tbx1 induces bone phenotypes similar to cleidocranial dysplasia. Hum. Mol. Genet. 2015, 24, 424–435.
  34. Funato, N.; Srivastava, D.; Shibata, S.; Yanagisawa, H. TBX1 Regulates Chondrocyte Maturation in the Spheno-occipital Synchondrosis. J. Dent. Res. 2020, 99, 1182–1191.
  35. Solot, C.B.; Sell, D.; Mayne, A.; Baylis, A.L.; Persson, C.; Jackson, O.; McDonald-McGinn, D.M. Speech-Language Disorders in 22q11.2 Deletion Syndrome: Best Practices for Diagnosis and Management. Am. J. Speech-Lang. Pathol. 2019, 28, 984–999.
  36. Jaouadi, A.; Tabebi, M.; Abdelhedi, F.; Abid, D.; Kamoun, F.; Chabchoub, I.; Maatoug, S.; Doukali, H.; Belghuith, N.; Ksentini, M.A.; et al. A novel TBX1 missense mutation in patients with syndromic congenital heart defects. Biochem. Biophys. Res. Commun. 2018, 499, 563–569.
  37. Zweier, C.; Sticht, H.; Aydin-Yaylagül, I.; Campbell, C.E.; Rauch, A. Human TBX1 Missense Mutations Cause Gain of Function Resulting in the Same Phenotype as 22q11.2 Deletions. Am. J. Hum. Genet. 2007, 80, 510–517.
  38. Hasegawa, K.; Tanaka, H.; Higuchi, Y.; Hayashi, Y.; Kobayashi, K.; Tsukahara, H. Novel heterozygous mutation in TBX1 in an infant with hypocalcemic seizures. Clin. Pediatr. Endocrinol. 2018, 27, 159–164.
  39. Alghamdi, M.; Al Khalifah, R.; Al Homyani, D.K.; Alkhamis, W.H.; Arold, S.T.; Ekhzaimy, A.; El-Wetidy, M.; Kashour, T.; Halwani, R. A novel TBX1 variant causing hypoparathyroidism and deafness. J. Endocr. Soc. 2020, 4, bvz028.
  40. Ogata, T.; Niihori, T.; Tanaka, N.; Kawai, M.; Nagashima, T.; Funayama, R.; Nakayama, K.; Nakashima, S.; Kato, F.; Fukami, M.; et al. TBX1 mutation identified by exome sequencing in a Japanese family with 22q11.2 deletion syndrome-like craniofacial features and hypocalcemia. PLoS ONE 2014, 9, e91598.
  41. Paylor, R.; Glaser, B.; Mupo, A.; Ataliotis, P.; Spencer, C.; Sobotka, A.; Sparks, C.; Choi, C.H.; Oghalai, J.; Curran, S.; et al. Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: Implications for 22q11 deletion syndrome. Proc. Natl. Acad. Sci. USA 2006, 103, 7729–7734.
  42. Rauch, R.; Hofbeck, M.; Zweier, C.; Koch, A.; Zink, S.; Trautmann, U.; Hoyer, J.; Kaulitz, R.; Singer, H.; Rauch, A. Comprehensive genotype-phenotype analysis in 230 patients with tetralogy of Fallot. J. Med. Genet. 2010, 47, 321–331.
  43. Stark, K.L.; Xu, B.; Bagchi, A.; Lai, W.-S.; Liu, H.; Hsu, R.; Wan, X.; Pavlidis, P.; Mills, A.A.; Karayiorgou, M.; et al. Altered brain microRNA biogenesis contributes to phenotypic deficits in a 22q11-deletion mouse model. Nat. Genet. 2008, 40, 751–760.
  44. Edelmann, L.; Stankiewicz, P.; Spiteri, E.; Pandita, R.K.; Shaffer, L.; Lupski, J.R.; Morrow, B.E.; Lupski, J. Two functional copies of the DGCR6 gene are present on human chromosome 22q11 due to a duplication of an ancestral locus. Genome Res. 2001, 11, 208–217.
  45. Hierck, B.P.; Molin, D.G.M.; Boot, M.J.; Poelmann, R.E.; Gittenberger-De Groot, A.C. A chicken model for DGCR6 as a modifier gene in the DiGeorge critical region. Pediatr. Res. 2004, 56, 440–448.
  46. Gao, S.; Moreno, M.; Eliason, S.; Cao, H.; Li, X.; Yu, W.; Bidlack, F.B.; Margolis, H.C.; Baldini, A.; Amendt, B.A. TBX1 protein interactions and microRNA-96-5p regulation controls cell proliferation during craniofacial and dental development: Implications for 22q11.2 deletion syndrome. Hum. Mol. Genet. 2015, 24, 2330–2348.
  47. Sun, H.; Jiang, P. MicroRNA-451a acts as tumor suppressor in cutaneous basal cell carcinoma. Mol. Genet. Genom. Med. 2018, 6, 1001–1009.
  48. Wang, J.; Bai, Y.; Li, H.; Greene, S.B.; Klysik, E.; Yu, W.; Schwartz, R.J.; Williams, T.J.; Martin, J.F. MicroRNA-17-92, a direct Ap-2alpha transcriptional target, modulates T-box factor activity in orofacial clefting. PLoS Genet. 2013, 9, e1003785.
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NORIKO FUNATO
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