Complementary Deoxyribonucleic Acid Cloning of an mRNA Encoding Transforming Growth Factor-beta 2 from Chicken Embryo Chondrocytes

被引:49
作者
Jakowlew, Sonia B. [1 ]
Dillard, Pamela J. [1 ]
Sporn, Michael B. [1 ]
Roberts, Anita B. [1 ]
机构
[1] NCI, Lab Chemoprevent, NIH, Bldg 41,Rm C629, Bethesda, MD 20892 USA
关键词
TGF-beta; 2; mRNA; cDNA cloning; chicken chondrocytes;
D O I
10.3109/08977199009071499
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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.
引用
收藏
页码:123 / 133
页数:11
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