引导先锋

IF 12.9 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Nature chemical biology Pub Date : 2024-11-18 DOI:10.1038/s41589-024-01786-z
Grant Miura
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引用次数: 0

摘要

叉头盒蛋白 A1(FOXA1)是一种先驱转录因子,它能与染色质上的典型 DNA motif 结合。这种结合可促进染色质的开放,为其他转录因子提供通道。用小分子靶向 FOXA1 等转录因子可作为一种有用的工具,用于阐明转录调控的快速动态,但由于缺乏可确定的结合口袋,这种靶向仍很困难。通过使用亲电化合物库进行基于活性的蛋白质分析化学筛选,Won 等人发现 WX-02-23 是 FOXA1 在 Wing2 区域一个特定半胱氨酸残基(C258)上的共价结合剂,已知该残基与 DNA 小沟有接触。WX-02-23 与 FOXA1 结合需要 DNA 的存在,并能增强 FOXA1-DNA 的相互作用。ChIP-seq(染色质免疫共沉淀测序)和ATAC-seq(利用测序分析转座酶可及染色质)分析表明,WX-02-23与FOXA1的C258依赖性结合可增加或减少整个基因组的FOXA1结合,这与染色质可及性的改变有关。研究小组发现,WX-02-23 改变了 10% 的 FOXA1 结合位点。基序分析表明,WX-02-23介导的这些增加的FOXA1结合位点缺乏典型基序的辅助性3 bp成分。他们提出,WX-02-23 可能会放松 FOXA1 识别的 DNA 主题,从而扩大其在细胞中的结合位点。定量 NanoBRET 检测证实,WX-02-23 增加了 FOXA1 与非规范基序的结合,这在 FOXA1 的 Wing2 区域(R261G)发生癌症热点突变时也能看到。虽然 WX-02-23 对 FOXA1 先驱活性的影响的结构基础仍不清楚,但 WX-02-23 的鉴定为揭示 FOXA1 生物学和染色质调控的新见解提供了一个多功能工具:Mol.Cell https://doi.org/10.1016/j.molcel.2024.09.024 (2024)
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Guiding the pioneer

Forkhead box protein A1 (FOXA1) is a pioneer transcription factor that binds to chromatin at a canonical DNA motif. This binding promotes the opening of chromatin, providing access to additional transcription factors. Targeting transcription factors such as FOXA1 with small molecules can serve as a useful tool to elucidate the rapid dynamics of transcriptional regulation, but remains difficult owing to a lack of definable binding pockets. Through a chemical screen using activity-based protein profiling with a library of electrophilic compounds, Won et al. identified WX-02-23 as a covalent binder of FOXA1 at a specific cysteine residue (C258) in the Wing2 region that is known to make contacts with the minor DNA groove. Binding of WX-02-23 to FOXA1 required the presence of DNA and enhanced FOXA1–DNA interactions. ChIP–seq (chromatin immunoprecipitation with sequencing) and ATAC-seq (assay for transposase-accessible chromatin using sequencing) analysis demonstrated that C258-dependent binding of WX-02-23 to FOXA1 can either increase or decrease FOXA1 binding throughout the genome, correlating with alterations in chromatin accessibility. The team found that WX-02-23 altered 10% of FOXA1 binding sites. Motif analysis revealed that these increased FOXA1 binding sites, mediated by WX-02-23, lack an ancillary 3 bp component of the canonical motif. They proposed that WX-02-23 may relax the DNA motif recognized by FOXA1 to expand its binding sites in cells. Quantitative NanoBRET assays confirmed that WX-02-23 increased FOXA1 binding to non-canonical motifs, which was also seen with a hotspot cancer mutation in the Wing2 region of FOXA1 (R261G). Although the structural basis for the effects of WX-02-23 on FOXA1 pioneering activity remain unclear, the identification of WX-02-23 offers a versatile tool to reveal new insights into FOXA1 biology and chromatin regulation.

Original reference: Mol. Cell https://doi.org/10.1016/j.molcel.2024.09.024 (2024)

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来源期刊
Nature chemical biology
Nature chemical biology 生物-生化与分子生物学
CiteScore
23.90
自引率
1.40%
发文量
238
审稿时长
12 months
期刊介绍: Nature Chemical Biology stands as an esteemed international monthly journal, offering a prominent platform for the chemical biology community to showcase top-tier original research and commentary. Operating at the crossroads of chemistry, biology, and related disciplines, chemical biology utilizes scientific ideas and approaches to comprehend and manipulate biological systems with molecular precision. The journal embraces contributions from the growing community of chemical biologists, encompassing insights from chemists applying principles and tools to biological inquiries and biologists striving to comprehend and control molecular-level biological processes. We prioritize studies unveiling significant conceptual or practical advancements in areas where chemistry and biology intersect, emphasizing basic research, especially those reporting novel chemical or biological tools and offering profound molecular-level insights into underlying biological mechanisms. Nature Chemical Biology also welcomes manuscripts describing applied molecular studies at the chemistry-biology interface due to the broad utility of chemical biology approaches in manipulating or engineering biological systems. Irrespective of scientific focus, we actively seek submissions that creatively blend chemistry and biology, particularly those providing substantial conceptual or methodological breakthroughs with the potential to open innovative research avenues. The journal maintains a robust and impartial review process, emphasizing thorough chemical and biological characterization.
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