Abstract
T-box genes are defined by the presence of a conserved sequence, the so-called T-box; this codes for the T-domain, which is involved in DNA-binding and protein dimerisation. Members of this gene family have been found in all metazoans, from diploblasts to humans, and mutations in T-box gene family members in humans have been linked to several congenital disorders. Sequencing of the complete genomes of a range of invertebrate and vertebrate species has allowed the classification of individual T-box genes into five subfamilies: Brachyury, T-brain I, Tbx I, Tbx2 and Tbx6. This review will largely focus on T-box genes identified in organisms whose genomes have been fully sequenced, emphasising how comparative studies of the T-box gene family will help to reveal the roles of these genes during development and in the adult. © Henry Stewart Publications.
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Minguillon, C., & Logan, M. (2003). The comparative genomics of T-box genes. Briefings in Functional Genomics and Proteomics, 2(3), 224–233. https://doi.org/10.1093/bfgp/2.3.224
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