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腺病毒E1A蛋白通过多个独立结构域作用于SAGA转录调控复合物,而非ADA转录调控复合物。

The adenovirus E1A protein targets the SAGA but not the ADA transcriptional regulatory complex through multiple independent domains.

作者信息

Shuen Michael, Avvakumov Nikita, Walfish Paul G, Brandl Chris J, Mymryk Joe S

机构信息

Department of Microbiology and Immunology, London Regional Cancer Centre, The University of Western Ontario, 709 Commissioners Road E., London, Ontario N6A 4L6, Canada.

出版信息

J Biol Chem. 2002 Aug 23;277(34):30844-51. doi: 10.1074/jbc.M201877200. Epub 2002 Jun 17.

Abstract

Expression of the adenovirus E1A protein in the simple eukaryote Saccharomyces cerevisiae inhibits growth. We tested four regions of E1A that alter growth and transcription in mammalian cells for their effects in yeast when expressed as fusions to the Gal4p DNA binding domain. Expression of the N-terminal/conserved region (CR) 1 or CR3, but not of the CR2 or the C-terminal portion of E1A, inhibited yeast growth. Growth inhibition was relieved by deletion of the genes encoding the yGcn5p, Ngg1p, or Spt7p components of the SAGA transcriptional regulatory complex, but not the Ahc1p component of the related ADA complex, indicating that the N-terminal/CR1 and CR3 regions of E1A target the SAGA complex independently. Expression of the pCAF acetyltransferase, a mammalian homologue of yGcn5p, also suppressed growth inhibition by either portion of E1A. Furthermore, the N-terminal 29 residues and the CR3 portion of E1A interacted independently with yGcn5p and pCAF in vitro. Thus, two separate regions of E1A target the yGcn5p component of the SAGA transcriptional activation complex. A subregion of the N-terminal/CR1 fragment spanning residues 30-69 within CR1 also inhibited yeast growth in a SAGA-dependent fashion. However, this region did not interact with yGcn5p or pCAF, suggesting that it makes a third contact with another SAGA component. Our results provide a new model system to elucidate mechanisms by which E1A and the SAGA complex regulate transcription and growth.

摘要

腺病毒E1A蛋白在简单真核生物酿酒酵母中的表达会抑制其生长。我们测试了E1A的四个在哺乳动物细胞中可改变生长和转录的区域,当它们与Gal4p DNA结合结构域融合表达时在酵母中的作用。E1A的N端/保守区域(CR)1或CR3的表达会抑制酵母生长,而CR2或E1A的C端部分的表达则不会。通过缺失编码SAGA转录调节复合物的yGcn5p、Ngg1p或Spt7p组分的基因可缓解生长抑制,但缺失相关ADA复合物的Ahc1p组分则不能,这表明E1A的N端/CR1和CR3区域独立靶向SAGA复合物。yGcn5p的哺乳动物同源物pCAF乙酰转移酶的表达也可抑制E1A任一部分引起的生长抑制。此外,E1A的N端29个残基和CR3部分在体外分别与yGcn5p和pCAF相互作用。因此,E1A的两个独立区域靶向SAGA转录激活复合物的yGcn5p组分。N端/CR1片段中跨越CR1内30 - 69位残基的一个亚区域也以SAGA依赖的方式抑制酵母生长。然而,该区域不与yGcn5p或pCAF相互作用,这表明它与SAGA的另一个组分形成了第三种相互作用。我们的结果提供了一个新的模型系统,以阐明E1A和SAGA复合物调节转录和生长的机制。

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