MOLECULAR-CLONING, GENETIC-MAPPING, AND DEVELOPMENTAL EXPRESSION OF ABOVINE TRANSFORMING-GROWTH-FACTOR-BETA (TGF-BETA) TYPE-I RECEPTOR

Citation
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
Citations number
44
Categorie Soggetti
Reproductive Biology","Developmental Biology",Biology,"Cell Biology
ISSN journal
1040452X
Volume
49
Issue
1
Year of publication
1998
Pages
1 - 9
Database
ISI
SICI code
1040-452X(1998)49:1<1:MGADEO>2.0.ZU;2-B
Abstract
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.