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腺病毒蛋白与视网膜母细胞瘤蛋白(pRB)和p53的相互作用。

Interaction of adenoviral proteins with pRB and p53.

作者信息

Moran E

机构信息

Cold Spring Harbor Laboratory, New York 11724.

出版信息

FASEB J. 1993 Jul;7(10):880-5. doi: 10.1096/fasebj.7.10.8344487.

Abstract

The transforming gene products of the small DNA tumor viruses subvert host cell growth control mechanisms by binding to specific cell regulatory proteins. These include the retinoblastoma gene product (pRB) and p53. One indication of the pivotal roles played by these regulatory products is the observation that they are each targeted consistently by viruses of several groups, by adenoviruses, the human papillomaviruses, and the papovaviruses. In adenovirus, pRB and p53 are targeted by the E1A and E1B genes, respectively. The genetic probes made possible by manipulation of the virus genes in vitro have helped to illuminate the pathways in which pRB and p53 function. E1A studies have contributed to our current understanding that the retinoblastoma product is one of a family of related proteins, which with associated cyclins and kinases can modulate the activity of the cellular E2F transcription factor. E1B studies have helped explore models of p53 function, including the suggestion that p53, probably through aspects of its transcription regulating activity, can initiate a pathway in which programmed cell death can be invoked to stop unrestricted cell proliferation.

摘要

小型DNA肿瘤病毒的转化基因产物通过与特定的细胞调节蛋白结合来颠覆宿主细胞的生长控制机制。这些调节蛋白包括视网膜母细胞瘤基因产物(pRB)和p53。这些调节产物发挥关键作用的一个迹象是,观察到它们分别被几个病毒组的病毒持续靶向,包括腺病毒、人乳头瘤病毒和乳多空病毒。在腺病毒中,pRB和p53分别被E1A和E1B基因靶向。通过体外操纵病毒基因而得以实现的基因探针,有助于阐明pRB和p53发挥功能的途径。对E1A的研究使我们目前认识到,视网膜母细胞瘤产物是相关蛋白家族的一员,它与相关的细胞周期蛋白和激酶一起,可以调节细胞E2F转录因子的活性。对E1B的研究有助于探索p53的功能模型,包括一种观点,即p53可能通过其转录调节活性的某些方面,启动一条可以引发程序性细胞死亡以阻止不受限制的细胞增殖的途径。

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