4.8 Article

Chromatin Fiber Invasion and Nucleosome Displacement by the Rap1 Transcription Factor

期刊

MOLECULAR CELL
卷 77, 期 3, 页码 488-+

出版社

CELL PRESS
DOI: 10.1016/j.molcel.2019.10.025

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资金

  1. Swiss National Science Foundation (SNSF) [31003A_173169, 31003A 170153]
  2. European Research Council (ERC) [724022]
  3. National Centre of Competence (NCCR) in Chemical Biology
  4. Ecole Polytechnique Federale de Lausanne (EPFL)
  5. Republic of Geneva
  6. Canton of Geneva
  7. European Research Council (ERC) [724022] Funding Source: European Research Council (ERC)
  8. Swiss National Science Foundation (SNF) [31003A_170153] Funding Source: Swiss National Science Foundation (SNF)

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Pioneer transcription factors (pTFs) bind to target sites within compact chromatin, initiating chromatin remodeling and controlling the recruitment of downstream factors. The mechanisms by which pTFs overcome the chromatin barrier are not well understood. Here, we reveal, using single-molecule fluorescence, how the yeast transcription factor Rap1 invades and remodels chromatin. Using a reconstituted chromatin system replicating yeast promoter architecture, we demonstrate that Rap1 can bind nucleosomal DNA within a chromatin fiber but with shortened dwell times compared to naked DNA. Moreover, we show that Rap1 binding opens chromatin fiber structure by inhibiting inter-nucleosome contacts. Finally, we reveal that Rap1 collaborates with the chromatin remodeler RSC to displace promoter nucleosomes, paving the way for long-lived bound states on newly exposed DNA. Together, our results provide a mechanistic view of how Rap1 gains access and opens chromatin, thereby establishing an active promoter architecture and controlling gene expression.

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