The DnaJ domain of polyomavirus large T antigen is required to regulate Rb family tumor suppressor function

被引:75
作者
Sheng, Q
Denis, D
Ratnofsky, M
Roberts, TM
DeCaprio, JA
Schaffhausen, B
机构
[1] TUFTS UNIV,SCH MED,DEPT BIOCHEM,BOSTON,MA 02111
[2] DANA FARBER CANC INST,BOSTON,MA 02115
关键词
D O I
10.1128/JVI.71.12.9410-9416.1997
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Tumor suppressors of the retinoblastoma susceptibility gene family regulate cell growth and differentiation, Polyomavirus large T antigens (large T) bind Rb family members and block their function, Mutations of large T sequences conserved with the DnaJ family affect large T binding to a cellular DnaK, heat shock protein 70, The same mutations abolish large T activation of E2F-containing promoters and Rb binding-dependent large T activation of cell cycle progression, Cotransfection of a cellular DnaJ domain blocks wild-type large T action, showing that the connection between the chaperone system and tumor suppressors is direct, Although they are inactive in assays dependent on Rb family binding, mutants in the J region retain the ability to associate with pRb, p107, and p130. This suggests that binding of Rb family members by large T is not sufficient for their inactivation and that a functional J domain is required as well, This work connects the DnaJ and DnaK molecular chaperones to regulation of tumor suppressors by polyomavirus large T.
引用
收藏
页码:9410 / 9416
页数:7
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