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Complementary deoxyribonucleic acid cloning of an mRNA encoding transforming growth factor-beta 2 from chicken embryo
S B Jakowlew1, P J Dillard, M B Sporn
1Laboratory of Chemoprevention, National Cancer Institute, NIH, Bethesda, Maryland 20892.
Abstract:
Using a simian transforming growth factor-beta 2 (TGF-beta 2) cDNA probe, we have isolated chicken cDNA clones for TGF-beta 2 from a chicken embryo chondrocyte cDNA library. The predicted precursor protein of chicken TGF-beta 2 is 412 amino acids long, two amino acids shorter than the human form to which it shows 90% identity. Cleavage of the chicken TGF-beta 2 precursor at a pentabasic Arg-Arg-Lys-Lys-Arg site would produce a 112-amino acid processed peptide differing by only one amino acid from the human TGF-beta 2 peptide. In contrast to TGF-beta 3 and 4 mRNAs, TGF-beta 2 mRNA is expressed in both cultured and non-cultured chicken embryo chondrocytes and at higher levels in chicken embryo fibroblasts. In chondrocytes and fibroblasts, the 3.9- and 4.3-kb TGF-beta 2 mRNAs are both expressed at higher levels than the 8-kb TGF-beta 2 mRNA; however, in developing chicken embryos, the level of expression of the 8-kb mRNA is higher than that of the 3.9- and 4.3-kb mRNAs.