Batchu R B, Shammas M A, Wang J Y, Munshi N C
Central Arkansas Veterans Health Care System and Myeloma and Transplantation Research Center, University of Arkansas for Medical Sciences, Little Rock, Arkansas 72205, USA.
J Biol Chem. 2001 Jun 29;276(26):24315-22. doi: 10.1074/jbc.M008154200. Epub 2001 Apr 6.
E2F-1, a major cellular transcription factor, plays a pivotal role in regulating the cell cycle. The activity of E2F-1 is negatively regulated by its interaction with retinoblastoma protein (pRB), and disruption of the pRB-E2F-1 complex, a hallmark of cellular transformation by DNA tumor viruses, leads to cell proliferation. Adeno-associated virus-2 (AAV) is known to have onco-suppressive properties against DNA tumor viruses. Here we provide, for the first time, the molecular basis for antioncogenic activity of AAV. Rep78, a major regulatory protein of AAV, interacts at the protein level with E2F-1 and stabilizes the pRB-E2F-1 complex. At the DNA level, Rep78 binds to a putative site on the E2F-1 promoter and down-regulates the adenovirus-induced E2F-1 transcription. This dual level of Rep78 activity leads to decreased cellular levels of free E2F-1, leading to its onco-suppressive properties.
E2F-1是一种主要的细胞转录因子,在调节细胞周期中起关键作用。E2F-1的活性通过其与视网膜母细胞瘤蛋白(pRB)的相互作用受到负调控,而pRB-E2F-1复合物的破坏是DNA肿瘤病毒导致细胞转化的一个标志,会导致细胞增殖。已知腺相关病毒2型(AAV)对DNA肿瘤病毒具有抑癌特性。在此,我们首次提供了AAV抗癌活性的分子基础。Rep78是AAV的一种主要调节蛋白,在蛋白质水平上与E2F-1相互作用并稳定pRB-E2F-1复合物。在DNA水平上,Rep78与E2F-1启动子上的一个假定位点结合,并下调腺病毒诱导的E2F-1转录。Rep78活性的这种双重作用导致细胞中游离E2F-1水平降低,从而产生其抗癌特性。