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Review

Craniofacial Phenotypes and Genetics of DiGeorge Syndrome

by
Noriko Funato
Department of Signal Gene Regulation, Advanced Therapeutic Sciences, Medical and Dental Sciences, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University (TMDU), Tokyo 113-8510, Japan
J. Dev. Biol. 2022, 10(2), 18; https://0-doi-org.brum.beds.ac.uk/10.3390/jdb10020018
Submission received: 21 April 2022 / Revised: 11 May 2022 / Accepted: 11 May 2022 / Published: 13 May 2022
(This article belongs to the Special Issue Scientific Papers by Developmental Biologists in Japan)
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Abstract

:
The 22q11.2 deletion is one of the most common genetic microdeletions, affecting approximately 1 in 4000 live births in humans. A 1.5 to 2.5 Mb hemizygous deletion of chromosome 22q11.2 causes DiGeorge syndrome (DGS) and velocardiofacial syndrome (VCFS). DGS/VCFS are associated with prevalent cardiac malformations, thymic and parathyroid hypoplasia, and craniofacial defects. Patients with DGS/VCFS manifest craniofacial anomalies involving the cranium, cranial base, jaws, pharyngeal muscles, ear-nose-throat, palate, teeth, and cervical spine. Most craniofacial phenotypes of DGS/VCFS are caused by proximal 1.5 Mb microdeletions, resulting in a hemizygosity of coding genes, microRNAs, and long noncoding RNAs. TBX1, located on chromosome 22q11.21, encodes a T-box transcription factor and is a candidate gene for DGS/VCFS. TBX1 regulates the fate of progenitor cells in the cranial and pharyngeal apparatus during embryogenesis. Tbx1-null mice exhibit the most clinical features of DGS/VCFS, including craniofacial phenotypes. Despite the frequency of DGS/VCFS, there has been a limited review of the craniofacial phenotypes of DGC/VCFS. This review focuses on these phenotypes and summarizes the current understanding of the genetic factors that impact DGS/VCFS-related phenotypes. We also review DGS/VCFS mouse models that have been designed to better understand the pathogenic processes of DGS/VCFS.

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 review focuses on these phenotypes and summarizes the current understanding of the genetic factors that impact DGS/VCFS-related phenotypes. We 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 (Figure S1, 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].
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 [37]. 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 [37]. 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. In this review, we focus on the 22q11.2 locus, its associated genes, and miRNAs.
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 [16,17]. The majority of clinical phenotypes of DGS/VCFS are caused by proximal 1.5 Mb microdeletions [3,22], 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 and Figure S2A). 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]. The coding variants in the T-box and C-terminal domains of TBX1 showed high combined annotation-dependent depletion (CADD) scores (Table S1); however, further investigation is required to confirm that the variants cause DGS/VCFS and how they impact the phenotypes.

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 [45]. DGCR6 and DGCR6L genes encode a protein with a sequence similar to the Drosophila gonadal [46] (Figure S2B). In a chicken model, targeting DGCR6 function resulted in a vascular phenotype [47]. 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 [47]. 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 [48]. miR-451a, a tumor suppressor, also directly targets TBX1 [49]. The expression of this gene is upregulated in cutaneous basal cell carcinoma, inversely to miR-451a [49]. miR-17-92 fine-tunes the expression of Tbx1 in craniofacial development, suggesting miR-17-92 as a candidate genetic modifier for Tbx1 [50]. 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 and Table S2). When these genes were analyzed according to biological process, “heart morphogenesis” and “cranial skeletal system development” were enriched (Table S3). Our enrichment analysis using ToppCluster [51] 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 and Table S2). These are described below.

4.1. Tbx1

Craniofacial structures with DGS/VCFS phenotypes are derivatives of the head mesenchyme and the first and second pharyngeal arches [62]. Tbx1 is expressed in the mesoderm, ectoderm, and endoderm of the pharyngeal apparatus and head mesenchyme between embryonic day (E)9.5 and E11.5 in mice [62,63]. At E12.5, Tbx1 is expressed in the oral epithelium, the myogenic core of the tongue, incisor tooth buds, pharyngeal muscles, and otic vesicle epithelium [63,64]. Tbx1-null mice exhibit the most clinical features of DGS/VCFS, while Tbx1+/− mice exhibit no significant craniofacial phenotypes (Table 2, Table 5 and Table S2). Information about ocular phenotypes in Tbx1-mutant mice is limited (Table 2), although these anomalies in patients with DGS/VCFS have been reported [16,17]. The Cre/loxP system has been used with Tbx1 conditional knockout mice to examine the tissue-specific function of TBX1 in craniofacial development (Table 5).

4.1.1. Cleft Palate

During palatogenesis, the palatal shelves develop bilaterally from the internal parts of the maxillary prominences and fuse above the tongue to form an intact oral cavity roof [67,68]. Because the palate consists of a bone-lined hard palate and a bone-free soft palate, cleft palate phenotypes include incomplete and submucosal cleft palates [67,68]. Ablation of Tbx1, which is expressed in the epithelium of the palatal shelves, results in abnormal intraoral epithelial fusions between the palatal shelves and the mandible, resulting in various degrees of the cleft palate phenotype (complete, incomplete, and submucosal cleft palate) [30,34,69]. Expression of Pax9, whose mutations lead to cleft palate and tooth agenesis [70], is downregulated in the palatal shelves and pharyngeal region of Tbx1-null embryos [34,71]. In Tbx1-null palatal shelves, muscle- and bone-related genes are downregulated, whereas neuron- and collagen biosynthesis-related genes are upregulated [72].

4.1.2. Abnormalities in Craniofacial Bones

Tbx1-null mice display craniofacial bone abnormalities, including persistently open fontanelles, micrognathia, a short clavicle, a hypoplastic zygomatic arch, and the absence of the hyoid bone (Table 2 and Table S2). Conditional deletion of Tbx1 in the mesoderm or osteochondral progenitors recapitulates the calvarial and mandibular phenotypes of Tbx1-null mice [35,66], suggesting that Tbx1 is required for morphogenesis and ossification of craniofacial bones. Although Tbx1 expression has not been reported in the neural crest, conditional deletion of Tbx1 here results in a hypoplastic hyoid bone [35] (Table 2 and Table 5). These results indicate that Tbx1 is required for the morphogenesis and ossification of mesoderm- and neural crest-derived membranous bones, although malformations observed in most neural crest-derived bones of Tbx1-null mice are secondary defects induced by non-neural crest cells [35,66]. Interestingly, abnormalities in membranous bones observed in Tbx1-null mice are similar to those of cleidocranial dysplasia (OMIM #119600 and #216330) in humans, exhibiting hypoplastic membranous bones, including abnormal neurocranial morphology, a short clavicle, a hypoplastic zygomatic arch, and hyoid bone [73,74,75]. Cleidocranial dysplasia (OMIM #119600) is caused by heterozygous mutations in RUNX2, which encodes a master transcription factor for osteoblast differentiation [74,75]. Since ablation of Tbx1 affects Runx2 expression in calvarial bones, and TBX1 overexpression induces Runx2 expression in vitro [35], TBX1 may act upstream of Runx2 by maintaining cell populations that express Runx2 at the onset of bone development. In addition, TBX1 could be a candidate gene for recessive inheritance of cleidocranial dysplasia (OMIM #216330).

4.1.3. Abnormalities in the Cranial Base and Cervical Spine

The spheno-occipital synchondrosis (SOS) in the cranial base is a vital growth center for the skull (reviewed in [76]). TBX1 is expressed in the mesoderm-derived cartilage primordium of the SOS and basioccipital bones, and Tbx1 deletion in the mesoderm induces malformed basioccipital bones and precocious ossified SOS. This indicates that Tbx1 is an essential regulator of chondrocyte differentiation and subsequent ossification at the SOS [36]. TBX1 inhibits the transcriptional activity of RUNX2 in vitro as well as the expression of RUNX2 target genes in SOS [36]. Tbx1-null mice also exhibit endochondral bone abnormalities in the atlas, axis, and xiphoid process [6,35]. There is potential to examine the phenotypes of cranial synchondroses in DGS/VCFS patients, as abnormalities in the SOS and basioccipital bones may induce cranial phenotypes of DGS/VCFS, such as dolichocephaly, basilar impression, and platybasia.

4.1.4. Dental Anomalies

Dental abnormalities (single central incisors, enamel hypoplasia, and small teeth) have been reported in many patients [18,28]. Accordingly, in approximately 30% of Tbx1-null mice, the upper incisors are absent [6]. Tbx1 is expressed in the cervical loops, which contain the dental stem cell niche in mice. The cervical loop region of the incisor is either severely reduced or completely absent in Tbx1-null mice, and cultured incisors of Tbx1-null mice are hypoplastic and lack enamel [77]. Ablation of Tbx1 in the epithelium results in smaller teeth than in the wild type, suggesting that TBX1 regulates the proliferation of dental progenitor cells [48].

4.1.5. Muscle Hypotonia

Branchiomeric muscles are derived from the mesoderm of the pharyngeal arch. In Tbx1-null and Tbx1flox/-;Mesp1-Cre embryos, the masseter, pterygoid, and temporalis muscles are intermittently absent [78,79]. Accordingly, muscle-related genes are also downregulated in Tbx1-null palatal shelves [72]. Tbx1 acts upstream of critical transcription factors to form branchiomeric muscles. These include LIM homeobox protein 2 (Lhx2), transcription factor 21 (Tcf21/capsulin), musculin (Msc), myogenic factor 5 (Myf5), myogenic differentiation 1 (Myod1), myocyte enhancer factor 2C (Mef2c), and GATA binding protein 4 (Gata4) [79,80,81,82]. Tbx1 is in the downstream genetic pathways of Tcf21, paired-like homeodomain transcription factor 2 (Pitx2), and ISL LIM homeobox 1 (Isl1) [80,83,84]. Thus, TBX1 regulates the pattern and development of branchiomeric muscles through the transcriptional regulation of myogenic genes.

4.2. Chordin (Chrd) and Transforming Growth Factor, Beta Receptor II (Tgfbr2)

Mice lacking the Chrd gene encoding chordin, an antagonist of bone morphogenetic proteins (BMPs), exhibit recapitulating phenotypes in Tbx1-null mice [32,52] (Table S2). Chrd-null neonates exhibit most craniofacial phenotypes in the cranium, cranial base, maxilla, mandible, ears, and hyoid bone (Table S2). Both Tbx1 and Fgf8 were reduced in the endoderm of Chrd-null mice, indicating that Chrd acts upstream of Tbx1 and Fgf8 [52]. Tbx1 acts upstream of SMAD family member 7 (Smad7), an inhibitory Smad within the BMP/TGFβ pathway, to regulate vascular smooth muscle and extracellular matrix investment of the fourth arch artery [85]. Conditional deletion of Tgfbr2, which encodes TGFβ receptor 2, in the neural crest resulted in DGS/VCFS-related cardiovascular defects [53]. These findings suggest a potential role of BMP/TGFβ signaling in the pathogenesis of DGS/VCFS.

4.3. Vascular Endothelial Growth Factor A (Vegfa)

VEGFA is an essential cytokine in angiogenesis and vascular development during embryogenesis [86]. Vegfa-null neonates exhibit a few aspects of DGS/VCFS-related craniofacial anomalies, including unfused cranial sutures, absent incisors, and short mandibles, as well as cardiovascular abnormalities [54] (Table S2). The deletion of Vegfa in mice reduces Tbx1 expression, and the knockdown of vegfaa/vegfa levels in zebrafish enhances the pharyngeal arch malformations induced by tbx1 knockdown [54]. In humans, low expression of the VEGFA haplotype increases the risk of a cardiac phenotype of DGS/VCFS, indicating that expression levels of VEGFA affect the severity of DGS/VCFS phenotypes [87]. These results suggest that VEGFA modifies DGS/VCFS-related phenotypes by regulating TBX1 expression.

4.4. Fibroblast Growth Factor 8 (Fgf8) and FGF Receptor 2 (Fgfr2)

Ablation of Fgf8 induces craniofacial, cardiovascular, thymic, and parathyroid phenotypes [55,88]. Fgf8-null neonates exhibit a few aspects of DGS/VCFS-related craniofacial anomalies, including cleft palate and abnormal outer ear morphology [55,88] (Table S2). Fgf8+/−;Tbx1+/− double heterozygous embryos show an increased penetrance of cardiovascular defects compared with Tbx1-heterozygous embryos [89]. Tissue-specific deletion of Fgf8 in Tbx1-expressing domains results in cardiovascular anomalies [90]. TBX1 activates the Fgf8 enhancer during cardiac development [9]. Deletion of the Fgfr2 gene that encodes FGF receptor 2 decreases Tbx1 expression in the dental epithelium, indicating a genetic link between FGF signaling and Tbx1 in tooth development [91]. In addition, a Tbx1-Six1/Eya1-Fgf8 genetic pathway is crucial for craniofacial morphogenesis [92,93]. These findings demonstrate that the FGF pathway and Tbx1 interact genetically during pharyngeal arch development.

4.5. CRK like Proto-Oncogene, Adaptor Protein (Crkl)

CRKL maps to the 2.5 Mb region commonly deleted in DGS/VCFS (Figure 1). Variants in a predicted enhancer of CRKL are significantly associated with the risk of congenital heart defects in DGS/VCFS [94]. Approximately 12% of Crkl-null mice show mild cranial bone defects, such as small cranium and poor membranous ossification of the nasal bones [56]. Compound heterozygosity of Crkl and Tbx1 in mice has revealed that Crkl deletion enhances DGS/VCFS-related abnormalities compared with Tbx1-heterozygous embryos [56], suggesting that Tbx1 and Crkl genes act in the same genetic pathway. CRKL encodes an adaptor protein that promotes the intracellular response of FGF signaling. Crkl+/−;Fgf8+/− double heterozygous mice showed DGS/VCFS-related defects [95]. Thus, CRKL mutations cause or modify DGS/VCFS-related phenotypes and/or penetrance as a contiguous gene syndrome.

4.6. Aldehyde Dehydrogenase Family 1, Subfamily A2 (Aldh1a2/Raldh2)

Retinoic acid (RA), an active vitamin A derivative, is essential for various developmental processes in vertebrates. High levels of RA act as morphogens that cause phenocopies of DGS/VCFS by downregulating Tbx1 expression in the pharyngeal apparatus [96,97]. RA levels are balanced by the RA-synthesizing enzyme aldehyde dehydrogenase (ALDH) and the Cyp26 RA-catabolizing enzyme [98,99]. Mouse embryos hypomorphic for Aldh1a2/Raldh2 display DGS/VCFS-related cardiovascular, thymic, and parathyroid malformations [57]. Haploinsufficiency of Aldh1a2/Raldh2 results in reduced embryonic synthesis of RA, increased levels of Tbx1, and accelerated recovery from arterial growth delay in Tbx1-heterozygous mice [100]. An inhibitor of the Cyp26 enzyme induces a phenocopy of DGS/VCFS in chick embryos [101]. In Tbx1-null mice, upregulated expression of Aldh1a2/Raldh2 and downregulated expression of Cyp26a1 have been observed [71].
Further interactions occur between RA signaling, Crkl, and Tbx1. The penetrance of thymic hypoplasia is reduced in Crkl+/−;Tbx1+/−;Aldh1a2+/− triple heterozygous embryos compared to Crkl+/−;Tbx1+/− mutants, suggesting that reducing the amount of RA may rescue the DGS/VCFS-related phenotype [102]. Thus, the levels of RA in embryogenesis could contribute to the phenotypic variability of DGS/VCFS.

4.7. Homeobox A3 (Hoxa3)

RA exposure increases the expression of Hoxa3, a gene which encodes a homeobox transcription factor, in the neural tube and pharyngeal apparatus [103]. Interestingly, Hoxa3-null neonates show some aspects of the abnormalities of DGS/VCFS [58,104] (Table S2). Thus, HOXA3 may be a genetic modifier of DGS/VCFS-related abnormalities.

4.8. Kat6a/Moz/Myst3 (Lysine Acetyltransferase 6A) and Epigenetic Modifiers

Homozygous mutation of Kat6a/Moz/Myst3, which encodes a histone acetyltransferase, leads to cardiovascular defects seen in DGS/VCFS and reduces Tbx1 expression [59]. Treatment of pregnant mice with a histone demethylase inhibitor reportedly increased the methylation levels of histone H3 lysine K4 (H3K4) and partially rescued the cardiovascular phenotypes of Tbx1-heterozygous mice [105]. TBX1 regulates genes transcribed at a low level by recruiting lysine methyltransferase (KMT2C) and controlling monomethylation of H3K4 (H3K4me1) enrichment on chromatin [105]. In addition, TBX1 transcriptionally targets Wnt5a by interacting with SMARCD1/BAF60a, a component of the SWI/SNF-like BAF chromatin remodeling complex, along with the H3K4 monomethyltransferase SETD7 [106]. Microduplication in KANSL1, which encodes a member of the histone acetyltransferase complex, is associated with heart anomalies in individuals with DGS/VCFS [107]. In T cells of patients with DGS/VCFS, the status of transcriptional activation (H3K4me3 and H3K27ac) is globally increased [108]. Thus, epigenetic changes are involved in DGS/VCFS-related phenotypes.

4.9. Sonic Hedgehog (Shh)

Shh encodes an SHH signaling molecule. In humans, SHH mutations lead to holoprosencephaly 3 (OMIM #142945), microphthalmia with coloboma (OMIM #611638), and single median maxillary central incisor (OMIM #147250). Shh-null embryos exhibit conotruncal and pharyngeal arch artery defects similar to those observed in DGS/VCFS and Tbx1-null embryos [109]. Tbx1 expression is reduced in Shh-null embryos, and ectopic expression of Shh can result in the upregulation of Tbx1, suggesting that Shh is a possible modifier for DGS/VCFS [62,110]. Shh is also required for the expression of the Fox family of transcription factor genes, forkhead box A2 (Foxa2) and forkhead box C2 (Foxc2), in the head mesenchyme and the pharyngeal endoderm [62]. FOXA2 and FOXC2 bind to regulatory regions in the mouse and human TBX1 loci [111].

4.10. Paired-like Homeodomain Transcription Factor 2 (Pitx2)

Pitx2 gene encodes a bicoid-like homeodomain transcription factor. Pitx2-null mice show craniofacial defects, such as the arrest of tooth development, abnormal morphology of maxilla and mandible, and cleft palate. In humans, PITX2 mutations lead to Axenfeld–Rieger syndrome, type 1 (OMIM #180500). Patients with Axenfeld–Rieger syndrome manifest dental and craniofacial anomalies involving the maxilla, mandible, and cranial base [112]. Both Tbx1 and Pitx2 are expressed in the early dental epithelium, oral epithelium, and secondary heart field [64,113,114]. Tbx1+/−;Pitx2+/− double heterozygous embryos exhibit increased penetrance of an extra premolar-like tooth [115] and DGS/VCFS-related cardiovascular anomalies [114]. TBX1 directly activates the Pitx2c enhancer through the synergistic action of the homeobox-containing transcription factor NK2 homeobox 5 (NKX2-5) [114]. TBX1 also interacts with PITX2 and represses PITX2 transcriptional activity [48,115]. Thus, PITX2 may be a genetic modifier of DGS/VCFS-related abnormalities.

5. Discussion

The penetrance and severity of congenital anomalies are related to genetic and environmental factors. Recent studies have revealed the function of TBX1 and modifiers that impact the severity and penetrance of DGS/VCFS. Studies of DGS/VCFS mouse models have provided insights into signaling pathways and genes that interact with TBX1 and/or affect the DGS/VCFS phenotypes. In addition, mouse models with DGS/VCFS may help us to identify additional DGS/VCFS-related phenotypes. For example, there is potential to examine the phenotypes of cranial synchondroses, cranium, zygomatic arches, and pharyngeal muscles in DGS/VCFS patients. We also noted that information about ocular phenotypes in Tbx1-mutant mice is limited, although these anomalies in patients with DGS/VCFS have been reported [16,17]. Crosstalk with key embryonic signals, especially BMP, TGFβ, VEGFA, FGF, RA, and SHH, critically regulates DGS/VCFS-related pharyngeal development. Genes involved in these signaling pathways may modify the phenotypic spectrum of DGS/VCFS. Given the broad spectrum of DGS/VCFS disease phenotypes, other genes essential to craniofacial development could modify the phenotypic spectrum. Genetically engineered mice are useful for studying disease phenotypes; however, ablation of essential genes involved in cardiovascular development may cause early embryonic lethality, which would prevent observation of craniofacial phenotypes. For example, ablation of Ufd1, whose human ortholog has been mapped to the 1.5 Mb region, causes early embryonic lethality before organogenesis in mice [116]. It is also essential to identify novel proteins that interact with TBX1 and examine whether interacting partners may influence the phenotypes of mouse models.

6. Conclusions

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.

Supplementary Materials

The following are available online at https://0-www-mdpi-com.brum.beds.ac.uk/article/10.3390/jdb10020018/s1, Figure S1: Craniofacial and skeletal phenotypes of DGS/VCFS. Figure S2: Human genes in the proximal deletion of 1.5 Mb on the 22q11.2 locus. Table S1: Craniofacial and skeletal phenotypes of DGS/VCFS and Tbx1-null mice. Table S2: Craniofacial and skeletal phenotypes in mouse models of DGS/VCFS. Table S3: Classification of mouse genes associated with DGS/VCFS.

Author Contributions

N.F. contributed to the conceptual idea, performed the database searches, analyzed the data, and wrote the manuscript. All authors have read and agreed to the published version of the manuscript.

Funding

This work was supported by the Japan Society for the Promotion of Science (JSPS) KAKENHI [20K09901].

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Acknowledgments

We would like to thank Hiroshi Kurosaka, Cedric Boeckx, and Mizuki Funato for a critical reading of the manuscript.

Conflicts of Interest

The author declares no conflict of interest.

References

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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.
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.
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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.
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.
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Table
Table 1. Craniofacial anomalies in patients with DGS/VCFS.
Table 1. Craniofacial anomalies in patients with DGS/VCFS.
PhenotypesFeaturesFrequency
Palatal anomaliesOvert cleft palate7–11%
Submucous cleft palate5–23%
Bifid uvula5–10%
Velopharyngeal insufficiency27–92%
Dental anomaliesTooth agenesis15%
Hypoplasia of primary teeth32%
Hypoplasia of permanent teeth10%
Enamel hypomineralization of primary teeth39%
Enamel hypomineralization of permanent teeth41%
Ear-nose-throat abnormalitiesHearing loss33–39%
Otitis media with effusion2%
Tracheomalacia/laryngomalacia2%
Laryngeal web1%
Ocular abnormalitiesHooding of the upper lid41%
Ptosis9%
Hooding of the lower lid6%
Epicanthal folds3%
Distichiasis3%
Cranial base anomaliesPlatybasia50–91%
Basilar impression3%
Cervical spine anomaliesAtlas (C1) anomalies75%
Axis (C2) anomalies59%
Fusion of C2–C334%
Data were summarized from the following references: [16,17,18,19,20,21,22].
Table
Table 2. Craniofacial and skeletal phenotypes of DGS/VCFS and Tbx1-null mice.
Table 2. Craniofacial and skeletal phenotypes of DGS/VCFS and Tbx1-null mice.
DGS/VCFSTbx1-Null Mice
CraniumDolichocephalySmall cranium
Abnormal skull morphologyHypoplastic parietal bone
Malar flatteningHypoplastic interparietal bone
Long faceUnfused cranial sutures between frontal and parietal bones
Temporal bone hypoplasia
Absent zygomatic arch
Abnormal zygomatic arch morphology
Cranial BasePlatybasiaAbnormal fusion of the basioccipital and basisphenoid bones
Basilar impressionAbnormal presphenoid bone morphology
Abnormal basioccipital bone morphology
PalateCleft palateCleft palate
Submucous cleft palateSubmucous cleft palate
Bifid uvulaBifid uvula
Highly arched palate
Velopharyngeal insufficiency
MandibleRetrognathiaAbsent mandibular coronoid process
Short mandibleShort mandible
MicrognathiaMicrognathia
TeethEnamel hypoplasiaAbnormal upper incisor morphology
Single central incisorAbsent upper incisors
Small teeth
Abnormality of the dentition
Carious teeth
MusclesPharyngeal hypotoniaAbsent masseter muscle
Absent pterygoid muscle
Absent temporalis muscle
EyesHypertelorism/telecanthusHypertelorism
Downslanted palpebral fissures
Proptosis
Strabismus
Abnormal eyelid morphology
Epicanthus
Microphthalmia
External EarsSmall earlobeEar lobe hypoplasia
Low-set ears Lowered ear position
Abnormally folded pinna Abnormal ear shape
Preauricular pitAbsent outer ear
Anotia
Middle and Inner EarsChronic otitis mediaAbnormal middle ear ossicle morphology
Conductive hearing lossAbsent middle ear ossicles
Sensorineural hearing lossAbnormal stapes morphology
Auditory canal stenosisAbnormal incus morphology
Pulsatile tympanic membraneAbnormal malleus morphology
Thickened tympanic membraneAbsent stapes
Tympanic membrane retractionAbnormal external auditory canal morphology
Decreased tympanic ring size
NoseProminent nasal bridgeShort snout
Abnormal nasal morphology
Underdeveloped nasal alae
Choanal atresia
ThroatAbnormal thorax morphologySmall thyroid cartilage
Abnormality of the pharynxSmall cricoid cartilage
Abnormal thyroid cartilage morphology
Pharynx hypoplasia
Hyoid bonesDelayed development of the hyoid boneHyoid bone hypoplasia
Invisible hyoid ossification centerAbnormal hyoid bone morphology
Cervical spine Dysmorphic C1Abnormal cervical atlas (C1) morphology
Anterior arch cleft of C1Absent arcus anterior of C1
Open posterior arch C1
Fusion of C1–C2
Fusion of C2–C3
Upswept C2 lamina
Platyspondyly
Others Short clavicle
References[14,15,16,17,18,19,20,21,22,23,24,25,26,27,28][6,7,8,9,10,29,30,31,32,33,34,35,36]
Data were summarized from the following references [6,7,8,9,10,14,15,16,17,18,19,20,21,22,23,24,25,26,27,28,29,30,31,32,33,34,35,36], OMIM (https://www.omim.org accessed on 3 August 2021) and the Monarch Initiative (https://monarchinitiative.org accessed on 3 August 2021).
Table
Table 3. DGS/VCFS-associated variants of TBX1.
Table 3. DGS/VCFS-associated variants of TBX1.
MutationDomainConditionCraniofacial AnomaliesReferences
c.89_284del N-terminalDiGeorge syndromeYesClinVar Variant: 971780
c.199_224del N-terminalDiGeorge syndromeYesClinVar Variant: 949172
c.292A>T N-terminalDiGeorge syndromeYesClinVar Variant: 526036
c.385G>A T-boxTetralogy of FallotNoClinVar Variant: 488618
c.443T>A (F148Y)T-boxConotruncal anomaly face syndromeYes[5]
c.503T>C T-boxDiGeorge syndrome
Velocardiofacial syndrome
(Shprintzen syndrome)
Tetralogy of Fallot 		YesClinVar Variant: 973222
c.569C > A (P190Q) T-boxCongenital heart defectsNo[38]
c.582C>G (H194Q)T-boxVelocardiofacial syndromeYes[39]
c.928G>A (G310S)C-terminalDiGeorge syndromeYes[5]
c.967_977dup AACCCCGTGGCC-terminalThymic hypoplasia
Postaxial polydactyly of the right fifth toe 		No[40]
c.1158_1159delinsTC-terminalHypoparathyroidism and hypocalcemia
Facial asymmetry
Deafness		Yes[41]
c.1223delCC-terminalConotruncal anomaly face syndrome
Velocardiofacial syndrome		Yes[5]
c.1253delAC-terminalDiGeorge syndromeYes[42]
c.1320-1342del23bpC-terminalVelocardiofacial syndromeYes/No[43]
c.1399-1428dup30C-terminalTetralogy of Fallot
Scoliosis
Facial asymmetry
Upslanting palpebral fissures
Absent pulmonary valve
Isolated left pulmonary artery		Yes[44]
ClinVar (https://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/clinvar accessed on 3 August 2021).
Table
Table 4. Craniofacial phenotypes of DGS/VCFS mouse model.
Table 4. Craniofacial phenotypes of DGS/VCFS mouse model.
Gene SymbolInduced Mutation TypeCraniumPalateTeethMusclesEar-Nose-ThroatHyoid BonesCardio-Vascular
Tbx1NullYesYesYesYesYesYesYes
ChrdNullYesYesnrnrYesYesYes
Tgfbr2Deletion (Wnt1-Cre)YesYesnrnrnrnrYes
VegfaNullYesYesYesnrnrnrYes
Fgf8Hypomorphic alleleYesYesYesnrYesYesYes
CrklNullYesnrnrnrYesnrYes
Aldh1a2Hypomorphic allelenrnrnrnrYesYesYes
Hoxa3NullnrYesnrYesYesYesYes
Kat6aNullnrYesnrnrYesnrYes
Dicer1Deletion (Wnt1-Cre)YesnrnrnrnrnrYes
Plxnd1Single point mutationnrYesnrnrYesnrYes
Dock1UndefinednrnrnrnrYesnrYes
Ndst1Single point mutationnrnrnrnrYesnrYes
Prickle1Single point mutationYesYesnrnrYesnrYes
Trappc10UndefinedYesYesnrnrnrnrYes
Zfp366Single point mutationnrnrnrnrYesnrYes
Foxn1Intragenic deletionnrnrnrnrYesnrYes
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 [6,7,8,9,10,29,30,31,32,33,34,35,36,52,53,54,55,56,57,58,59,60,61]. nr, not reported. A detailed description is provided in Table S2.
Table
Table 5. Selected craniofacial phenotypes of Tbx1-mutant neonates.
Table 5. Selected craniofacial phenotypes of Tbx1-mutant neonates.
Tbx1-Mutant MiceCraniofacial Phenotypes
Mutation TypeTissue/CellCraniumCranial BasePalateMandibleHyoid BoneCervical Spine
Tbx1+/−Entire bodyNormalNormalNormalNormalNormalNormal
Tbx1-nullEntire bodyAbnormalAbnormalCPHypoplasticHypoplasticAbnormal
Deletion (Foxg1-Cre)Pharyngeal tissues *AbnormalAbnormalCPHypoplasticHypoplasticNA
Deletion (KRT14-Cre)EpitheliumNormalNormalAnterior CPNormalNormalNormal
Deletion (Mesp1-Cre) MesodermAbnormalAbnormalNAHypoplasticHypoplasticAbnormal
Deletion (Twist2-Cre)Osteochondral progenitorsAbnormalAbnormalNormalNormalHypoplasticAbnormal
Deletion (Wnt1-Cre) Neural crestNormalNormalNormalNormalHypoplasticNormal
Data were summarized from the following references: [30,31,34,35,36,65,66]. * pharyngeal pouches, otic and optic vesicles [30,31]; * pharyngeal endoderm, ectoderm, and mesoderm [65]; CP, cleft palate; NA, not available.
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Funato, N. Craniofacial Phenotypes and Genetics of DiGeorge Syndrome. J. Dev. Biol. 2022, 10, 18. https://0-doi-org.brum.beds.ac.uk/10.3390/jdb10020018

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Funato N. Craniofacial Phenotypes and Genetics of DiGeorge Syndrome. Journal of Developmental Biology. 2022; 10(2):18. https://0-doi-org.brum.beds.ac.uk/10.3390/jdb10020018

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Funato, Noriko. 2022. "Craniofacial Phenotypes and Genetics of DiGeorge Syndrome" Journal of Developmental Biology 10, no. 2: 18. https://0-doi-org.brum.beds.ac.uk/10.3390/jdb10020018

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