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由GAGA转录因子结合介导的热休克启动子处的ATP依赖性核小体破坏。

ATP-dependent nucleosome disruption at a heat-shock promoter mediated by binding of GAGA transcription factor.

作者信息

Tsukiyama T, Becker P B, Wu C

机构信息

Laboratory of Biochemistry, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892.

出版信息

Nature. 1994 Feb 10;367(6463):525-32. doi: 10.1038/367525a0.

Abstract

Genetic control elements are usually situated in local regions of chromatin that are hypersensitive to structural probes such as DNase I. We have reconstructed the chromatin structure of the hsp70 promoter using an in vitro nucleosome assembly system. Binding of the GAGA transcription factor on existing nucleosomes leads to nucleosome disruption, DNase I hypersensitivity at the TATA box and heat-shock elements, and rearrangement of adjacent nucleosomes. ATP hydrolysis facilitates this process, suggesting that an energy-dependent pathway is involved in chromatin remodelling.

摘要

遗传控制元件通常位于对诸如核酸酶I等结构探针高度敏感的染色质局部区域。我们利用体外核小体组装系统重建了hsp70启动子的染色质结构。GAGA转录因子与现有核小体的结合导致核小体破坏、TATA框和热休克元件处的核酸酶I超敏反应以及相邻核小体的重排。ATP水解促进了这一过程,表明染色质重塑涉及一个能量依赖途径。

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