Che-1 affects cell growth by interfering with the recruitment of HDAC1 by Rb

被引:69
|
作者
Bruno, T
De Angelis, R
De Nicola, F
Barbato, C
Di Padova, M
Corbi, N
Libri, V
Benassi, B
Mattei, E
Chersi, A
Soddu, S
Floridi, A
Passananti, C
Fanciulli, M
机构
[1] Regina Elena Inst Canc Res, Expt Res Ctr, Lab B, I-00158 Rome, Italy
[2] Regina Elena Inst Canc Res, Expt Res Ctr, Lab D, I-00158 Rome, Italy
[3] Regina Elena Inst Canc Res, Expt Res Ctr, Mol Oncogenesis Lab, I-00158 Rome, Italy
[4] Regina Elena Inst Canc Res, Expt Res Ctr, Expt Chemotherapy Lab, I-00158 Rome, Italy
[5] Univ Roma Tor Vergata, Dept Neurosci, I-00133 Rome, Italy
[6] Univ Aquila, Dept Expt Med, I-67100 Laquila, Italy
[7] CNR, Ist Tecnol Biomed, I-00137 Rome, Italy
关键词
D O I
10.1016/S1535-6108(02)00182-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
DNA tumor virus oncoproteins bind and inactivate Rb by interfering with the Rb/HDAC1 interaction. Che-1 is a recently identified human Rb binding protein that inhibits the Rb growth suppressing function. Here we show that Che-1 contacts the Rb pocket region and competes with HDAC1 for Rb binding site, removing HDAC1 from the Rb/E2F complex in vitro and from the E2F target promoters in vivo. Che-1 overexpression activates DNA synthesis in quiescent NIH-3T3 cells through HDAC1 displacement. Consistently, Che-1-specific RNA interference affects E2F activity and cell proliferation in human fibroblasts but not in the pocket protein-defective 293 cells. These findings indicate the existence of a pathway of Rb regulation supporting Che-1 as the cellular counterpart of DNA tumor virus oncoproteins.
引用
收藏
页码:387 / 399
页数:13
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