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在正常细胞增殖过程中,GAS41是抑制p53肿瘤抑制通路所必需的。

GAS41 is required for repression of the p53 tumor suppressor pathway during normal cellular proliferation.

作者信息

Park Jeong Hyeon, Roeder Robert G

机构信息

Laboratory of Biochemistry and Molecular Biology, The Rockefeller University, New York, NY 10021, USA.

出版信息

Mol Cell Biol. 2006 Jun;26(11):4006-16. doi: 10.1128/MCB.02185-05.

Abstract

GAS41 is a common subunit of the TIP60 and SRCAP complexes and is essential for cell growth and viability. Here, we report that GAS41 is required for repression of the p53 tumor suppressor pathway during normal cellular proliferation. Either GAS41 small interfering RNA-mediated knockdown of GAS41 expression or specific interruptions of the carboxy-terminal coiled-coil motif of the GAS41 protein activate the p53 tumor suppressor pathway, as evidenced by p53 up-regulation, p53 serine-15 phosphorylation, and p21 transcriptional activation. Activation of the p53 pathway does not result from changes in TIP60 complex assembly or TIP60 coactivator functions for p53, since a TIP60 complex containing a coiled-coil mutant of GAS41 retains the same composition and histone acetyltransferase activity as its wild-type counterpart and since mutant GAS41 does not compromise ectopic p53-dependent transcriptional activation in a reporter gene assay. Finally, we demonstrate that GAS41 is prebound to the promoters of two p53 tumor suppressor pathway genes (p21 and p14ARF) in normal unstressed cells but is dissociated from both promoters in response to stress signals that activate p53. Our data suggest that GAS41 plays a role in repressing the p53 tumor suppressor pathway during the normal cell cycle by a TIP60-independent mechanism.

摘要

GAS41是TIP60和SRCAP复合物的一个共同亚基,对细胞生长和存活至关重要。在此,我们报告在正常细胞增殖过程中,GAS41是抑制p53肿瘤抑制通路所必需的。GAS41小干扰RNA介导的GAS41表达敲低或GAS41蛋白羧基末端卷曲螺旋基序的特异性中断均会激活p53肿瘤抑制通路,这可通过p53上调、p53丝氨酸15磷酸化以及p21转录激活得以证明。p53通路的激活并非源于TIP60复合物组装的改变或TIP60对p53的共激活功能的改变,因为含有GAS41卷曲螺旋突变体的TIP60复合物与其野生型对应物具有相同的组成和组蛋白乙酰转移酶活性,且在报告基因检测中突变型GAS41不会损害异位p53依赖的转录激活。最后,我们证明在正常未受应激的细胞中,GAS41预先结合于两个p53肿瘤抑制通路基因(p21和p14ARF)的启动子上,但在响应激活p53的应激信号时会从这两个启动子上解离。我们的数据表明,GAS41在正常细胞周期中通过一种不依赖TIP60的机制在抑制p53肿瘤抑制通路中发挥作用。

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