J. Skonier, M. Neubauer, L. Madisen, K. Bennett, G. Plowman, A. F. Purchio, Bristol-Myers Squibb
1992.9.1DNA AND CELL BIOLOGY
tlooto Summary
DNA sequence analysis of βig-h3 indicated that it encoded a novel protein, βIG-H3, of 683 amino acids, which contained an amino-terminal secretory sequence and a carboxy-terminal Arg-Gly-Asp (RGD) sequence that can serve as a ligand recognition site for several integrins.
Abstract
ABSTRACT Transforming growth factor-β (TGF-β) is capable of affecting the proliferation of many cell types. To identify novel genes whose protein products may mediate cellular responses to this factor, a cDNA library was made from mRNA isolated from a human lung adenocarcinoma cell line (A549) that had been treated for 3 days with TGF-β. The library was screened by differential hybridization and a cDNA clone, βig-h3, was isolated. This gene was induced up to 20-fold in A549 cells after 2 days of treatment with TGF-β1. It was also induced in several other cell lines, including PC-3 and H2981. DNA sequence analysis of βig-h3 indicated that it encoded a novel protein, βIG-H3, of 683 amino acids, which contained an amino-terminal secretory sequence and a carboxy-terminal Arg-Gly-Asp (RGD) sequence that can serve as a ligand recognition site for several integrins. βIG-H3 also contained short amino acid regions homologous to similar regions in Drosophila fasciclin-I and four homologous internal domains, which c...
Citation format
SKONIER, J., et al. Cdna cloning and sequence analysis of βig-h3, a novel gene induced in a human adenocarcinoma cell line after treatment with transforming growth factor-β. DNA AND CELL BIOLOGY, 1992, 11: 511–522.