Baluchamy S, Sankar N, Navaraj A, Moran E, Thimmapaya B
Department of Microbiology-Immunology Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA.
Oncogene. 2007 Feb 1;26(5):781-7. doi: 10.1038/sj.onc.1209825. Epub 2006 Jul 24.
We recently showed that p300/CREB-binding protein (CBP) plays an important role in maintaining cells in G0/G1 phase by keeping c-myc in a repressed state. Consistent with this, adenovirus E1A oncoprotein induces c-myc in a p300-dependent manner, and the c-myc induction is linked to S-phase induction. The induction of S phase by E1A is dependent on its binding to and inactivating several host proteins including p300/CBP. To determine whether there is a correlation between the host proteins binding to the N-terminal region of E1A, activation of c-myc and induction of S phase, we assayed the c-myc and S-phase induction in quiescent human cells by infecting them with Ad N-terminal E1A mutants with mutations that specifically affect binding to different chromatin-associated proteins including pRb, p300, p400 and p300/CBP-associated factor (PCAF). We show that the mutants that failed to bind to p300 or pRb were severely defective for c-myc and S-phase induction. The induction of c-myc and S phase was only moderately affected when E1A failed to bind to p400. Furthermore, analysis of the E1A mutants that fail to bind to p300, and both p300 and PCAF suggests that PCAF may also play a role in c-myc repression, and that the two chromatin-associated proteins may repress c-myc independently. In summary, these results suggest that c-myc deregulation by E1A through its interaction with these chromatin-associated proteins is an important step in the E1A-mediated cell cycle deregulation and possibly in cell transformation.
我们最近发现,p300/CREB结合蛋白(CBP)通过使c-myc处于抑制状态,在维持细胞处于G0/G1期发挥重要作用。与此一致的是,腺病毒E1A癌蛋白以p300依赖的方式诱导c-myc,且c-myc的诱导与S期诱导相关。E1A对S期的诱导依赖于其与包括p300/CBP在内的几种宿主蛋白的结合及使其失活。为了确定与E1A N端区域结合的宿主蛋白、c-myc的激活和S期诱导之间是否存在关联,我们用Ad N端E1A突变体感染静止的人细胞,这些突变体发生了特异性影响与不同染色质相关蛋白(包括pRb、p300、p400和p300/CBP相关因子(PCAF))结合的突变,检测了c-myc和S期诱导情况。我们发现,未能与p300或pRb结合的突变体在c-myc和S期诱导方面存在严重缺陷。当E1A未能与p400结合时,c-myc和S期的诱导仅受到中度影响。此外,对未能与p300以及同时未能与p300和PCAF结合的E1A突变体的分析表明,PCAF可能也在c-myc的抑制中发挥作用,并且这两种染色质相关蛋白可能独立抑制c-myc。总之,这些结果表明,E1A通过与这些染色质相关蛋白的相互作用导致c-myc失调,是E1A介导的细胞周期失调以及可能的细胞转化中的重要一步。