Biology:T-box

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Short description: Genes that affect limb and heart development
T-box
1H6F.png
Crystallographic structure of the TBX3 protein dimer (cyan and green) complexed with DNA (brown) based on the PDB: 1h6f​ coordinates.
Identifiers
SymbolT-box
PfamPF00907
InterProIPR001699
PROSITEPS50252
SCOP21xbr / SCOPe / SUPFAM

T-box refers to a group of transcription factors involved in embryonic limb and heart development.[1] Every T-box protein has a relatively large DNA-binding domain, generally comprising about a third of the entire protein that is both necessary and sufficient for sequence-specific DNA binding. All members of the T-box gene family bind to the "T-box", a DNA consensus sequence of TCACACCT.[2]

Members

T-boxes are especially important to the development of embryos, found in zebrafish oocyte by Bruce et al 2003 and Xenopus laevis oocyte by Xanthos et al 2001. They are also expressed in later stages, including adult mouse and rabbit studied by Szabo et al 2000.[3]

Mutations in the first one found caused short tails in mice, and thus the protein encoded was named brachyury, Greek for "short-tail". In mice this gene is named Tbxt, and in humans it is named TBXT.[4][5] Brachyury has been found in all bilaterian animals that have been screened, and is also present in the cnidaria.[6]

The mouse Tbxt gene was cloned[7] and found to be a 436 amino acid embryonic nuclear transcription factor. The protein brachyury binds to the T-box through a region at its N-terminus.

Protein activity

The encoded proteins of TBX5 and TBX4 play a role in limb development, and play a major role in limb bud initiation specifically.[8] For instance, in chickens TBX4 specifies hindlimb status while Tbx5 specifies forelimb status.[9] The activation of these proteins by Hox genes initiates signaling cascades that involve the Wnt signaling pathway and FGF signals in limb buds.[8] Ultimately, TBX4 and TBX5 lead to the development of apical ectodermal ridge (AER) and zone of polarizing activity (ZPA) signaling centers in the developing limb bud, which specify the orientation growth of the developing limb.[8] Together, TBX5 and TBX4 play a role in patterning the soft tissues (muscles and tendons) of the musculoskeletal system.[10]

Defects

In humans, and some other animals, defects in the TBX5 gene expression are responsible for Holt–Oram syndrome, which is characterized by at least one abnormal wrist bone. Other arm bones are almost always affected, though the severity can vary widely, from complete absence of a bone, to only a reduction in bone length.[11][12] Seventy-five percent of affected individuals also have heart defects, most often there is no separation between the left and right ventricle of the heart.[13]

TBX3 is associated with ulnar–mammary syndrome in humans, but is also responsible for the presence or absence of dun color in horses, and has no deleterious effects whether expressed or not.[14]

T-box genes

Genes encoding T-box proteins include:


See also

References

  1. ↑ "The T-box family". Genome Biology 3 (6): REVIEWS3008. 2002. doi:10.1186/gb-2002-3-6-reviews3008. PMID 12093383. 
  2. ↑ Müller, CW; Herrmann, BG (23 October 1997). "Crystallographic structure of the T domain-DNA complex of the Brachyury transcription factor" (in en). Nature 389 (6653): 884–8. doi:10.1038/39929. PMID 9349824. Bibcode: 1997Natur.389..884M. 
  3. ↑ Naiche, L.A.; Harrelson, Zachary; Kelly, Robert G.; Papaioannou, Virginia E. (2005-12-01). "T-Box Genes in Vertebrate Development". Annual Review of Genetics (Annual Reviews) 39 (1): 219–239. doi:10.1146/annurev.genet.39.073003.105925. ISSN 0066-4197. PMID 16285859. 
  4. ↑ "Entrez Gene: T". https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=6862. 
  5. ↑ "The human homolog T of the mouse T(Brachyury) gene; gene structure, cDNA sequence, and assignment to chromosome 6q27". Genome Research 6 (3): 226–33. March 1996. doi:10.1101/gr.6.3.226. PMID 8963900. 
  6. ↑ "The ancestral role of Brachyury: expression of NemBra1 in the basal cnidarian Nematostella vectensis (Anthozoa)". Development Genes and Evolution 212 (12): 563–70. January 2003. doi:10.1007/s00427-002-0272-x. PMID 12536320. 
  7. ↑ "Cloning of the T gene required in mesoderm formation in the mouse". Nature 343 (6259): 617–22. February 1990. doi:10.1038/343617a0. PMID 2154694. Bibcode: 1990Natur.343..617H. 
  8. ↑ 8.0 8.1 8.2 "How the embryo makes a limb: determination, polarity and identity". Journal of Anatomy 227 (4): 418–30. October 2015. doi:10.1111/joa.12361. PMID 26249743. 
  9. ↑ "The T-box genes Tbx4 and Tbx5 regulate limb outgrowth and identity". Nature 398 (6730): 814–8. April 1999. doi:10.1038/19769. PMID 10235264. Bibcode: 1999Natur.398..814R. 
  10. ↑ "Tbx4 and tbx5 acting in connective tissue are required for limb muscle and tendon patterning". Developmental Cell 18 (1): 148–56. January 2010. doi:10.1016/j.devcel.2009.11.013. PMID 20152185. 
  11. ↑ "Holt–Oram syndrome". U.S. National Library of Medicine. June 2014. https://ghr.nlm.nih.gov/condition/holt-oram-syndrome. 
  12. ↑ McDermott DA, Fong JC, Basson CT. Holt–Oram Syndrome. 2004 Jul 20 [Updated 2015 Oct 8]. In Adam MP, Ardinger HH, Pagon RA, et al., editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2018. Available from: https://www.ncbi.nlm.nih.gov/books/NBK1111/
  13. ↑ Bossert, T; Walther, T; Gummert, J; Hubald, R; Kostelka, M; Mohr, FW (October 2002). "Cardiac malformations associated with the Holt–Oram syndrome—report on a family and review of the literature.". The Thoracic and Cardiovascular Surgeon 50 (5): 312–4. doi:10.1055/s-2002-34573. PMID 12375192. 
  14. ↑ "Regulatory mutations in TBX3 disrupt asymmetric hair pigmentation that underlies Dun camouflage color in horses". Nature Genetics 48 (2): 152–8. February 2016. doi:10.1038/ng.3475. PMID 26691985. 
    • "A horse of a different color: Genetics of camouflage and the dun pattern". ScienceDaily (Press release). December 21, 2015.

Further reading

External links




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