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一种在G0期细胞中重塑染色质结构的病毒机制。

A viral mechanism for remodeling chromatin structure in G0 cells.

作者信息

Ghosh Mrinal K, Harter Marian L

机构信息

Department of Molecular Biology, Lerner Research Institute, The Cleveland Clinic Foundation, Cleveland, OH 44195, USA.

出版信息

Mol Cell. 2003 Jul;12(1):255-60. doi: 10.1016/s1097-2765(03)00225-9.

Abstract

Small DNA viruses force quiescent cells to reenter the cell cycle in order to replicate their DNA. We report here that the adenovirus E1A protein creates an S phase environment in quiescent cells by overcoming the nucleosomal repression of E2F-targeted genes. These genes are surrounded by Lys-9-methylated H3 histones, and their promoters are occupied by the pRb-related protein p130 and the inhibitory transcription factor E2F4. Kinetic analysis indicates that E1A binds to E2F promoters where it eliminates p130 and E2F4, resulting in the dramatic elimination of H3 Lys-9 methylation. Thereafter, H3 Lys-9 acetylation occurs along with the recruitment of activating E2F family members, and this is followed by the transcriptional activity of E2F-targeted genes. These results indicate that E1A has a role in reconfiguring chromatin structure and that this activity is necessary to overcome the repressive mechanisms that maintain cells in a quiescent state.

摘要

小型DNA病毒迫使静止细胞重新进入细胞周期以复制其DNA。我们在此报告,腺病毒E1A蛋白通过克服E2F靶向基因的核小体抑制作用,在静止细胞中创造了一个S期环境。这些基因被赖氨酸-9甲基化的H3组蛋白所包围,其启动子被pRb相关蛋白p130和抑制性转录因子E2F4占据。动力学分析表明,E1A与E2F启动子结合,在那里它消除了p130和E2F4,导致H3赖氨酸-9甲基化显著消除。此后,H3赖氨酸-9乙酰化伴随着激活型E2F家族成员的募集而发生,随后是E2F靶向基因的转录活性。这些结果表明,E1A在重新配置染色质结构中发挥作用,并且这种活性对于克服维持细胞静止状态的抑制机制是必要的。

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