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先驱因子 GAF 与 PBAP(SWI/SNF)和 NURF(ISWI)合作调节转录。

Pioneer-like factor GAF cooperates with PBAP (SWI/SNF) and NURF (ISWI) to regulate transcription.

机构信息

Department of Molecular Biology and Genetics, Cornell University, Ithaca, New York 14853, USA.

Department of Stem Cell and Regenerative Biology, Harvard University, Cambridge, Massachusetts 02138, USA.

出版信息

Genes Dev. 2021 Jan 1;35(1-2):147-156. doi: 10.1101/gad.341768.120. Epub 2020 Dec 10.

Abstract

Transcriptionally silent genes must be activated throughout development. This requires nucleosomes be removed from promoters and enhancers to allow transcription factor (TF) binding and recruitment of coactivators and RNA polymerase II (Pol II). Specialized pioneer TFs bind nucleosome-wrapped DNA to perform this chromatin opening by mechanisms that remain incompletely understood. Here, we show that GAGA factor (GAF), a pioneer-like factor, functions with both SWI/SNF and ISWI family chromatin remodelers to allow recruitment of Pol II and entry to a promoter-proximal paused state, and also to promote Pol II's transition to productive elongation. We found that GAF interacts with PBAP (SWI/SNF) to open chromatin and allow Pol II to be recruited. Importantly, this activity is not dependent on NURF as previously proposed; however, GAF also synergizes with NURF downstream from this process to ensure efficient Pol II pause release and transition to productive elongation, apparently through its role in precisely positioning the +1 nucleosome. These results demonstrate how a single sequence-specific pioneer TF can synergize with remodelers to activate sets of genes. Furthermore, this behavior of remodelers is consistent with findings in yeast and mice, and likely represents general, conserved mechanisms found throughout eukarya.

摘要

转录沉默的基因必须在整个发育过程中被激活。这需要核小体从启动子和增强子中去除,以允许转录因子(TF)结合,并募集共激活因子和 RNA 聚合酶 II(Pol II)。专门的先驱 TF 结合核小体包裹的 DNA,通过仍然不完全理解的机制进行染色质开放。在这里,我们表明 GAGA 因子(GAF),一种先驱样因子,与 SWI/SNF 和 ISWI 家族染色质重塑因子一起发挥作用,允许 Pol II 的募集和进入启动子近端暂停状态,并促进 Pol II 向产性延伸的转变。我们发现 GAF 与 PBAP(SWI/SNF)相互作用以打开染色质并允许 Pol II 被募集。重要的是,这种活性以前所提出的并不依赖于 NURF;然而,GAF 也与 NURF 协同作用,在这个过程的下游,以确保 Pol II 暂停释放和产性延伸的有效转变,显然是通过其在精确定位+1 核小体中的作用。这些结果表明,单个序列特异性先驱 TF 如何与重塑因子协同激活基因集。此外,这种重塑因子的行为与酵母和小鼠中的发现一致,并且可能代表在整个真核生物中发现的普遍保守机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c196/7778264/4857075c1621/147f01.jpg

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