Wang S, Nath N, Adlam M, Chellappan S
Department of Pathology, College of Physicians and Surgeons, Columbia University, New York, NY 10032, USA.
Oncogene. 1999 Jun 10;18(23):3501-10. doi: 10.1038/sj.onc.1202684.
The retinoblastoma tumor suppressor protein and its family members, p107 and p130, are major regulators of the mammalian cell cycle. They exert their growth suppressive effects at least in part by binding the E2F family of transcription factors and inhibiting their transcriptional activity. Agents that disrupt the interaction between Rb family proteins and E2F promote cell proliferation. Here we describe the characterization of a novel interaction between Rb family proteins and a potential tumor suppressor protein, prohibitin. Prohibitin physically interacts with all three Rb family proteins in vitro and in vivo, and was very effective in repressing E2F-mediated transcription. Prohibitin could inhibit the activity of E2Fs 1, 2, 3, 4 and 5, but could not affect the activity of promoters lacking an E2F site. Surprisingly, prohibitin-mediated repression of E2F could not be reversed by adenovirus E1A protein. A prohibitin mutant that could not bind to Rb was impaired in its ability to repress E2F activity and inhibit cell proliferation. We believe that prohibitin is a novel regulator of E2F activity that responds to specific signaling cascades.
视网膜母细胞瘤肿瘤抑制蛋白及其家族成员p107和p130是哺乳动物细胞周期的主要调节因子。它们至少部分地通过结合转录因子E2F家族并抑制其转录活性来发挥生长抑制作用。破坏Rb家族蛋白与E2F之间相互作用的因子会促进细胞增殖。在此,我们描述了Rb家族蛋白与一种潜在的肿瘤抑制蛋白——抑制素之间新型相互作用的特征。抑制素在体外和体内均与所有三种Rb家族蛋白发生物理相互作用,并且在抑制E2F介导的转录方面非常有效。抑制素可以抑制E2F 1、2、3、4和5的活性,但不影响缺乏E2F位点的启动子的活性。令人惊讶的是,腺病毒E1A蛋白无法逆转抑制素介导的E2F抑制作用。一种无法与Rb结合的抑制素突变体在抑制E2F活性和抑制细胞增殖的能力上受损。我们认为抑制素是一种响应特定信号级联反应的新型E2F活性调节因子。