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TBX1

From Wikipedia, the free encyclopedia
TBX1
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesTBX1, CAFS, CATCH22, CTHM, DGCR, DGS, DORV, TBX1C, TGA, VCF, VCFS, T-box 1, T-box transcription factor 1
External IDsOMIM: 602054; MGI: 98493; HomoloGene: 7966; GeneCards: TBX1; OMA:TBX1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_005992
NM_080646
NM_080647
NM_001379200

NM_001285472
NM_001285476
NM_011532
NM_001373938

RefSeq (protein)

NP_005983
NP_542377
NP_542378
NP_001366129

NP_001272401
NP_001272405
NP_035662

Location (UCSC)Chr 22: 19.76 – 19.78 MbChr 16: 18.4 – 18.41 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

T-box transcription factor TBX1 also known as T-box protein 1 and testis-specific T-box protein is a protein that in humans is encoded by the TBX1 gene.[5] Genes in the T-box family are transcription factors that play important roles in the formation of tissues and organs during embryonic development.[6] To carry out these roles, proteins made by this gene family bind to specific areas of DNA called T-box binding element (TBE)[6] to control the expression of target genes.

Gene

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The TBX1 gene is located on the long (q) arm of chromosome 22 at position 11.21, from base pair 18,118,779 to base pair 18,145,669.[5]

Function

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The T-box 1 protein appears to be necessary for the normal development of large arteries that carry blood out of the heart, muscles and bones of the face and neck, and glands such as the thymus and parathyroid.[7][8] Although the T-box 1 protein acts as a transcription factor, it is not yet known which genes are regulated by the protein.

TBX1 is thought to operate on the same developmental pathway as CHD7 which can be mutated in CHARGE syndrome. [9]

Clinical significance

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Most cases of 22q11.2 deletion syndrome are caused by the deletion of a small piece of chromosome 22. This region of the chromosome contains about 30 genes, including the TBX1 gene. In a small number of affected individuals without a chromosome 22 deletion, mutations in the TBX1 gene are thought to be responsible for the characteristic signs and symptoms of the syndrome. Of the three known mutations, two mutations change one amino acid (a building block of proteins) in the T-box 1 protein. The third mutation deletes a single amino acid from the protein. These mutations likely disrupt the ability of the T-box 1 protein to bind to DNA and regulate the activity of other genes.[10][11][12]

Loss of the TBX1 gene, due to either a mutation in the gene or a deletion of part of chromosome 22, is responsible for many of the features of 22q11.2 deletion syndrome. Specifically, a loss of the TBX1 gene is associated with heart defects, an opening in the roof of the mouth (a cleft palate), distinctive facial features, and low calcium levels, but does not appear to cause learning disabilities.[13][14]

Mutation in TBX1 causes predisposition to hernias.[15]

References

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  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000184058Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000009097Ensembl, 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. ^ a b "Entrez Gene: T-box 1".
  6. ^ a b Bollag RJ, Siegfried Z, Cebra-Thomas JA, Garvey N, Davison EM, Silver LM (July 1994). "An ancient family of embryonically expressed mouse genes sharing a conserved protein motif with the T locus". Nature Genetics. 7 (3): 383–389. doi:10.1038/ng0794-383. PMID 7920656. S2CID 32296875.
  7. ^ Jerome LA, Papaioannou VE (March 2001). "DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1". Nature Genetics. 27 (3): 286–291. doi:10.1038/85845. PMID 11242110. S2CID 21030663.
  8. ^ Lindsay EA, Vitelli F, Su H, Morishima M, Huynh T, Pramparo T, et al. (March 2001). "Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice". Nature. 410 (6824): 97–101. doi:10.1038/35065105. PMID 11242049. S2CID 41144744.
  9. ^ Zhao Y, Wang Y, Shi L, McDonald-McGinn DM, Crowley TB, McGinn DE, et al. (July 2023). "Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS". npj Genomic Medicine. 8 (1): 17. doi:10.1038/s41525-023-00363-y. PMC 10354062. PMID 37463940.
  10. ^ Baldini A (October 2003). "DiGeorge's syndrome: a gene at last". Lancet. 362 (9393): 1342–1343. doi:10.1016/S0140-6736(03)14671-5. PMID 14585631. S2CID 37195058.
  11. ^ Baldini A (May 2004). "DiGeorge syndrome: an update". Current Opinion in Cardiology. 19 (3): 201–204. doi:10.1097/00001573-200405000-00002. PMID 15096950. S2CID 785356.
  12. ^ Yagi H, Furutani Y, Hamada H, Sasaki T, Asakawa S, Minoshima S, et al. (October 2003). "Role of TBX1 in human del22q11.2 syndrome". Lancet. 362 (9393): 1366–1373. doi:10.1016/S0140-6736(03)14632-6. PMID 14585638. S2CID 32995817.
  13. ^ Packham EA, Brook JD (April 2003). "T-box genes in human disorders". Human Molecular Genetics. 12. 12 Spec No 1 (Spec No 1): R37–R44. doi:10.1093/hmg/ddg077. PMID 12668595.
  14. ^ Yamagishi H, Srivastava D (September 2003). "Unraveling the genetic and developmental mysteries of 22q11 deletion syndrome". Trends in Molecular Medicine. 9 (9): 383–389. doi:10.1016/S1471-4914(03)00141-2. PMID 13129704.
  15. ^ Zhang Y, Han Q, Li C, Li W, Fan H, Xing Q, Yan B (February 2014). "Genetic analysis of the TBX1 gene promoter in indirect inguinal hernia". Gene. 535 (2): 290–293. doi:10.1016/j.gene.2013.11.012. PMID 24295890.

Further reading

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This article incorporates text from the United States National Library of Medicine, which is in the public domain.