Identification of rCop-1, a new member of the CCN protein family, as a negative regulator for cell transformation

被引:126
作者
Zhang, R
Averboukh, L
Zhu, WM
Zhang, H
Jo, H
Dempsey, PJ
Coffey, RJ
Pardee, AB
Liang, P
机构
[1] Vanderbilt Univ, Dept Cell Biol, Vanderbilt Canc Ctr, Nashville, TN 37232 USA
[2] Dana Farber Canc Inst, Div Cell Growth & Regulat, Boston, MA 02115 USA
关键词
D O I
10.1128/MCB.18.10.6131
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:6131 / 6141
页数:11
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