Identification of rCop-1, a New Member of the CCN Protein Family, as a Negative Regulator for Cell Transformation

Author:

Zhang Rong1,Averboukh Lidia2,Zhu Weimin2,Zhang Hong1,Jo Hakryul1,Dempsey Peter J.1,Coffey Robert J.1,Pardee Arthur B.2,Liang Peng1

Affiliation:

1. Vanderbilt Cancer Center, Department of Cell Biology, Vanderbilt University, Nashville, Tennessee 37232,1 and

2. Division of Cell Growth and Regulation, Dana-Farber Cancer Institute, Boston, Massachusetts 021152

Abstract

ABSTRACT By using a model system for cell transformation mediated by the cooperation of the activated H- ras oncogene and the inactivated p53 tumor suppressor gene, rCop-1 was identified by mRNA differential display as a gene whose expression became lost after cell transformation. Homology analysis indicates that rCop-1 belongs to an emerging cysteine-rich growth regulator family called CCN, which includes connective-tissue growth factor, CYR61, CEF10 (v- src inducible), and the product of the nov proto-oncogene. Unlike the other members of the CCN gene family, rCop-1 is not an immediate-early gene, it lacks the conserved C-terminal domain which was shown to confer both growth-stimulating and heparin-binding activities, and its expression is lost in cells transformed by a variety of mechanisms. Ectopic expression of rCop-1 by retroviral gene transfers led to cell death in a transformation-specific manner. These results suggest that rCop-1 represents a new class of CCN family proteins that have functions opposing those of the previously identified members.

Publisher

American Society for Microbiology

Subject

Cell Biology,Molecular Biology

Reference38 articles.

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