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

  • Cancer Cell. 2002 Nov;2(5):387-99. doi: 10.1016/s1535-6108(02)00182-4.
Tiziana Bruno  1 Roberta De Angelis Francesca De Nicola Christian Barbato Monica Di Padova Nicoletta Corbi Valentina Libri Barbara Benassi Elisabetta Mattei Alberto Chersi Silvia Soddu Aristide Floridi Claudio Passananti Maurizio Fanciulli
Affiliations
  • 1. Laboratory B, Via delle Messi d'Oro 156, 00158 Rome, Italy.
Abstract

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.