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核小体结合的 MuvB 转录因子复合物的结构揭示了 DNA 重塑。

Structure of a nucleosome-bound MuvB transcription factor complex reveals DNA remodelling.

机构信息

Division of Structural Biology, Chester Beatty Laboratories, The Institute of Cancer Research, London, UK.

Functional Proteomics, Chester Beatty Laboratories, Cancer Biology Division, The Institute of Cancer Research, London, UK.

出版信息

Nat Commun. 2022 Aug 29;13(1):5075. doi: 10.1038/s41467-022-32798-9.

Abstract

Genes encoding the core cell cycle machinery are transcriptionally regulated by the MuvB family of protein complexes in a cell cycle-specific manner. Complexes of MuvB with the transcription factors B-MYB and FOXM1 activate mitotic genes during cell proliferation. The mechanisms of transcriptional regulation by these complexes are still poorly characterised. Here, we combine biochemical analysis and in vitro reconstitution, with structural analysis by cryo-electron microscopy and cross-linking mass spectrometry, to functionally examine these complexes. We find that the MuvB:B-MYB complex binds and remodels nucleosomes, thereby exposing nucleosomal DNA. This remodelling activity is supported by B-MYB which directly binds the remodelled DNA. Given the remodelling activity on the nucleosome, we propose that the MuvB:B-MYB complex functions as a pioneer transcription factor complex. In this work, we rationalise prior biochemical and cellular studies and provide a molecular framework of interactions on a protein complex that is key for cell cycle regulation.

摘要

基因编码的核心细胞周期机制在细胞周期特异性的方式下被 MuvB 家族的蛋白质复合物转录调控。MuvB 与转录因子 B-MYB 和 FOXM1 的复合物在细胞增殖过程中激活有丝分裂基因。这些复合物的转录调控机制仍未得到很好的描述。在这里,我们结合生化分析和体外重组,以及冷冻电镜和交联质谱的结构分析,对这些复合物进行功能研究。我们发现 MuvB:B-MYB 复合物结合并重塑核小体,从而暴露核小体 DNA。这种重塑活性得到了 B-MYB 的支持,B-MYB 直接结合重塑的 DNA。鉴于核小体上的重塑活性,我们提出 MuvB:B-MYB 复合物作为一种先驱转录因子复合物。在这项工作中,我们合理化了先前的生化和细胞研究,并提供了一个对细胞周期调控至关重要的蛋白质复合物相互作用的分子框架。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0123/9424243/1def847a7202/41467_2022_32798_Fig1_HTML.jpg

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