Baj. Roelen et al., MOLECULAR-CLONING, GENETIC-MAPPING, AND DEVELOPMENTAL EXPRESSION OF ABOVINE TRANSFORMING-GROWTH-FACTOR-BETA (TGF-BETA) TYPE-I RECEPTOR, Molecular reproduction and development, 49(1), 1998, pp. 1-9
A full-length cDNA encoding the bovine transforming growth factor beta
(TGF-beta) receptor type I (bT beta R-I) was isolated from a placenta
cDNA library. The deduced protein sequence of 499 residues contains a
single transmembrane domain, a cysteine-rich extracellular domain, an
d an intracellular kinase domain with predicted serine/threonine speci
ficity. The amino acid sequence is 96% and 95% identical with its huma
n and mouse homologues, respectively. Genetic mapping assigned the TGF
BR1 gene to bovine chromosome 8 at a male genetic distance of 2 centim
organ from D8S28. Assuming conservation of gene order, the linkage dat
a define a breakpoint in mammalian chromosome evolution. Both TGF-beta
receptor type I and II mRNAs were found to be expressed in bovine ooc
ytes and preimplantation two-cell, four-cell, eight-cell, morula-, and
blastocyst-stage embryos, as determined by heminested reverse transcr
iption polymerase chain reaction (RT-PCR). The mRNA expression pattern
s of TGF-beta receptor types I, II, and III in a variety of bovine org
an tissues were examined by Northern blot hybridization, and highest l
evels were detected in lung and ovary. (C) 1998 Wiley-Liss, Inc.