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TBX22

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TBX22
Identifiers
AliasesTBX22,ABERS, CLPA, CPX, TBXX, dJ795G23.1, T-box 22, T-box transcription factor 22
External IDsOMIM:300307;MGI:2389465;HomoloGene:9666;GeneCards:TBX22;OMA:TBX22 - orthologs
Orthologs
SpeciesHumanMouse
Entrez

50945

245572

Ensembl

ENSG00000277800
ENSG00000122145

ENSMUSG00000031241

UniProt

Q9Y458

Q8K402

RefSeq (mRNA)

NM_001109878
NM_001109879
NM_001303475
NM_016954

NM_001290747
NM_145224
NM_181319

RefSeq (protein)

NP_001103348
NP_001103349
NP_001290404
NP_058650

NP_001277676
NP_660259
NP_851836

Location (UCSC)Chr X: 80.01 – 80.03 MbChr X: 106.71 – 106.73 Mb
PubMedsearch[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

T-box transcription factor TBX22is aproteinthat in humans is encoded by theTBX22gene.[5]

TBX22 is a member of a phylogenetically conserved family of proteins that share a common DNA-binding domain, theT-box.T-box genes encodetranscription factorsinvolved in the regulation of developmental processes. Mutations in this gene have been associated with the inherited X-linked disorder,cleft palatewithankyloglossia(tongue-tie), and it is believed to play a major role in human palatogenesis.[5]It has previously been mapped to the long arm of the X chromosome and it has now been demonstrated that mutations in the gene TBX22 are the cause of this syndrome.[6]TBX22 mutations also result in non-syndromiccleft palatein some populations.[7]

TBX22 is composed of seven exons spanning 8.7 kilobases of genomic DNA in Xq21.1. The TBX22 mRNA is 2099 base pairs long and encodes a 400-amino-acids protein containing a T-domain in its NH2-terminal region which has the unique feature of missing 20 amino-acids relative to the other known T-domains.[8]

Function[edit]

T-box genes are members of a family of transcriptional regulators that contain a region encoding a conserved DNA-binding motif of approximately 200 amino acids: the T-domain. These genes are grouped together on the basis of the homology existing between their products and the mouseBrachyury(or T) protein. In human and mouse, numerous T-domain-containing genes have been identified so far and mapped throughout the genome. The spatio-temporal expression of these genes is strictly regulated during the development of both vertebrates and invertebrates.[8]

Functional studies have demonstrated that several T-box genes are involved inmesodermspecification in the developing embryo of mouse orXenopus.In mice, the Brachyury gene is expressed in early mesoderm cells and its expression then becomes restricted to thenotochord.The Brachyury protein binds as a dimer to a 20-nucleotide partiallypalindromicsequence recognized by its T-domain. More generally, T-box genes have been shown to be critical during development for propermorphogenesisandorganogenesis.Abnormal expression of several T-box genes has been shown to cause developmental anomalies in mouse,Drosophilaor zebrafish.

Clinical significance[edit]

TBX22 mutations in two families predicted to have X linked cleft palate and ankyloglossia. Sequence electropherograms from genomic DNA amplified from exon 5 (family K) and exon 4 (family W) are of affected (mutant) males and unaffected (control) females. *Represents the site of the sequence variant.

In humans, two T-box genes are involved in inherited disorders: mutations in TBX5 causeHolt–Oram syndrome,whereas mutations in TBX3 causeulnar–mammary syndrome.[8]

Mutations in TBX22 cause X-linked cleft palate and ankyloglossia.[9]CPX has been described in a small number of families exhibiting a strong X linked Mendelian inheritance. The cleftphenotypepredominantly affects males who show variation ranging from a complete cleft of the secondary palate, submucous cleft, or bifid uvula to high arched palate. Ankyloglossia is frequently seen in affected patients and carrier females, and has proved to be a useful indicator of CPX. Temporal and spatial studies using in situ hybridization in both human and mouse has shown that TBX22/Tbx22 is expressed primarily in the palatal shelves and tongue duringpalatogenesis,indicating a specific role of TBX22 in both palatal and tongue development. In addition to families with well defined X linked inheritance, TBX22 mutations have been identified in several families where pedigree size and/or family history were too limited to predict mode of inheritance. In these cases, ascertainment was largely based on the presence of ankyloglossia as well as cleft palate.[10]

It has been demonstrated that TBX22 makes a significant contribution to the prevalence of cleft palate at least in the Brazilian and the North American cohorts.[8]To date, 10 different TBX22 mutations have been reported in patients with CP and/or ankyloglossia.[11]These include small deletions/insertions, nonsense, splice site, frameshift and missense alterations.[7]

References[edit]

  1. ^abcENSG00000122145 GRCh38: Ensembl release 89: ENSG00000277800, ENSG00000122145–Ensembl,May 2017
  2. ^abcGRCm38: Ensembl release 89: ENSMUSG00000031241–Ensembl,May 2017
  3. ^"Human PubMed Reference:".National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^"Mouse PubMed Reference:".National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ab"Entrez Gene: TBX22 T-box 22".
  6. ^Braybrook C, Doudney K, Marçano AC, et al. (2001). "The T-box transcription factor gene TBX22 is mutated in X-linked cleft palate and ankyloglossia".Nat. Genet.29(2): 179–83.doi:10.1038/ng730.PMID11559848.S2CID28939959.
  7. ^abSuphapeetiporn K, Tongkobpetch S, Siriwan P, Shotelersuk V (2008)."TBX22 mutations are a frequent cause of non-syndromic cleft palate in the Thai population".Clin. Genet.72(5): 478–83.doi:10.1111/j.1399-0004.2007.00891.x.PMID17868388.S2CID2244618.
  8. ^abcdLaugier-Anfossi F, Villard L (2000). "Molecular characterization of a new human T-box gene (TBX22) located in xq21.1 encoding a protein containing a truncated T-domain".Gene.255(2): 289–96.doi:10.1016/S0378-1119(00)00326-7.PMID11024289.
  9. ^Dixon MJ, Marazita ML, Beaty TH, Murray JC (March 2011)."Cleft lip and palate: understanding genetic and environmental influences".Nat. Rev. Genet.12(3): 167–78.doi:10.1038/nrg2933.PMC3086810.PMID21331089.
  10. ^Marçano AC, Doudney K, Braybrook C, et al. (2004)."TBX22 mutations are a frequent cause of cleft palate".J. Med. Genet.41(1): 68–74.doi:10.1136/jmg.2003.010868.PMC1757272.PMID14729838.
  11. ^Online Mendelian Inheritance in Man(OMIM):T-BOX 22; TBX22 - 300307

Further reading[edit]

External links[edit]

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