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The human homolog T of the mouse T(Brachyury) gene; gene structure, cDNA sequence, and assignment to chromosome 6q27.
Author(s) -
Yvonne H. Edwards,
W. Putt,
K M Lekoape,
David I. Stott,
M. Fox,
D. A. HOPKINSON,
Jane C. Sowden
Publication year - 1996
Publication title -
genome research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.556
H-Index - 297
eISSN - 1549-5469
pISSN - 1088-9051
DOI - 10.1101/gr.6.3.226
Subject(s) - brachyury , biology , notochord , gene , genetics , tbx1 , complementary dna , microbiology and biotechnology , mesoderm , gene expression , promoter , embryogenesis , embryonic stem cell
We have cloned the human gene encoding the transcription factor T. T protein is vital for the formation of posterior mesoderm and axial development in all vertebrates. Brachyury mutant mice, which lack T protein, die in utero with abnormal notochord, posterior somites, and allantois. We have identified human T genomic clones and derived the mRNA sequence and gene structure. There is 91% amino acid identity between human and mouse T proteins overall and complete identity across 77 amino acids of the T-box motif within the DNA-binding domain. Human T expression is very similar to that found for T in other vertebrate species and is confined to cells derived from the notochord. The human T gene maps to chromosome 6q27 and is only the second human member of the T-box gene family to be described.

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