{"title":"引导先锋","authors":"Grant Miura","doi":"10.1038/s41589-024-01786-z","DOIUrl":null,"url":null,"abstract":"<p>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.</p><p><b>Original reference:</b> <i>Mol. Cell</i> https://doi.org/10.1016/j.molcel.2024.09.024 (2024)</p>","PeriodicalId":18832,"journal":{"name":"Nature chemical biology","volume":"9 1","pages":""},"PeriodicalIF":12.9000,"publicationDate":"2024-11-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Guiding the pioneer\",\"authors\":\"Grant Miura\",\"doi\":\"10.1038/s41589-024-01786-z\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>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.</p><p><b>Original reference:</b> <i>Mol. Cell</i> https://doi.org/10.1016/j.molcel.2024.09.024 (2024)</p>\",\"PeriodicalId\":18832,\"journal\":{\"name\":\"Nature chemical biology\",\"volume\":\"9 1\",\"pages\":\"\"},\"PeriodicalIF\":12.9000,\"publicationDate\":\"2024-11-18\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Nature chemical biology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1038/s41589-024-01786-z\",\"RegionNum\":1,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nature chemical biology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1038/s41589-024-01786-z","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
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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