用Pioneer-seq定义转录因子核小体结合。

IF 3.7 2区 生物学 Q1 GENETICS & HEREDITY
PLoS Genetics Pub Date : 2025-08-14 eCollection Date: 2025-08-01 DOI:10.1371/journal.pgen.1011813
Maria Tsompana, Patrick D Wilson, Vijaya Murugaiyan, Christopher R Handelmann, Michael J Buck
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引用次数: 0

摘要

基因表达需要将转录因子(TFs)靶向于核小体中经常被封闭的调控序列。为了全面研究TF核小体结合,我们开发了Pioneer-Seq。在Pioneer-seq中,包含TF结合位点(TFBS)变体的序列在所有可能的核小体方向和连接区域内形成了数千个核小体的文库。Pioneer-seq具有独特的能力,可以同时检测由各种核小体定位序列产生的核小体,并检测与体内靶向核小体(itn)的结合。Pioneer-seq可用于直接解决tf -核小体结合的各种机制模型,并可用于揭示固有的tf -相互作用差异。为了证明Pioneer-seq,我们检测了OCT4、SOX2、KLF4和c-MYC与核小体的结合。我们的研究结果表明,所有研究的TF都可以在核小体边缘结合,核小体序列是调节TF结合的主要因素。此外,KLF4可以结合位于核小体二联体20 bp处的非规范TFBS。itn的检查显示tf之间的结合存在差异,KLF4和SOX2更常结合在核小体中心附近。总的来说,我们的研究结果证明了TF如何识别核小体内的TFBS的差异,并开始定义先锋因子结合的机制要求。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Defining transcription factor nucleosome binding with Pioneer-seq.

Gene expression requires the targeting of transcription factors (TFs) to regulatory sequences often occluded within nucleosomes. To comprehensively examine TF nucleosome binding, we developed Pioneer-Seq. In Pioneer-seq a library of thousands of nucleosomes are formed from sequences containing a TF binding site (TFBS) variant in all possible nucleosome orientations and within the linker regions. Pioneer-seq has the unique ability to simultaneously examine nucleosomes created with various nucleosome positioning sequences and examine binding to in vivo targeted nucleosomes (ITNs). Pioneer-seq can be applied to address various mechanistic models for TF-nucleosome binding directly and can be used to uncover inherent TF-interaction differences. To demonstrate Pioneer-seq, we examined nucleosome binding by OCT4, SOX2, KLF4, and c-MYC. Our results demonstrate that all studied TFs can bind at nucleosome edges and nucleosome sequence is the primary factor regulating TF binding. In addition, KLF4 can bind to a non-canonical TFBS located 20 bp from the nucleosome dyad. Examination of ITNs showed binding differences between the TFs, with KLF4 and SOX2 binding more often near nucleosome centers. Overall, our results demonstrate differences in how TF recognizes their TFBS within a nucleosome and begins to define the mechanistic requirements for pioneer factor binding.

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来源期刊
PLoS Genetics
PLoS Genetics GENETICS & HEREDITY-
自引率
2.20%
发文量
438
期刊介绍: PLOS Genetics is run by an international Editorial Board, headed by the Editors-in-Chief, Greg Barsh (HudsonAlpha Institute of Biotechnology, and Stanford University School of Medicine) and Greg Copenhaver (The University of North Carolina at Chapel Hill). Articles published in PLOS Genetics are archived in PubMed Central and cited in PubMed.
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