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Dynamic 1D search and processive nucleosome translocations by RSC and ISW2 chromatin remodelers.
Kim, Jee Min; Carcamo, Claudia C; Jazani, Sina; Xie, Zepei; Feng, Xinyu A; Yamadi, Maryam; Poyton, Matthew; Holland, Katie L; Grimm, Jonathan B; Lavis, Luke D; Ha, Taekjip; Wu, Carl.
Affiliation
  • Kim JM; Department of Biology, Johns Hopkins University, Baltimore, United States.
  • Carcamo CC; Department of Biophysics and Biophysical Chemistry, Johns Hopkins University School of Medicine, Baltimore, United States.
  • Jazani S; Department of Biophysics and Biophysical Chemistry, Johns Hopkins University School of Medicine, Baltimore, United States.
  • Xie Z; Department of Biology, Johns Hopkins University, Baltimore, United States.
  • Feng XA; Department of Biology, Johns Hopkins University, Baltimore, United States.
  • Yamadi M; Department of Biophysics and Biophysical Chemistry, Johns Hopkins University School of Medicine, Baltimore, United States.
  • Poyton M; Department of Biology, Johns Hopkins University, Baltimore, United States.
  • Holland KL; Department of Biology, Johns Hopkins University, Baltimore, United States.
  • Grimm JB; Janelia Research Campus, Howard Hughes Medical Institute, Ashburn, United States.
  • Lavis LD; Janelia Research Campus, Howard Hughes Medical Institute, Ashburn, United States.
  • Ha T; Janelia Research Campus, Howard Hughes Medical Institute, Ashburn, United States.
  • Wu C; Department of Biophysics and Biophysical Chemistry, Johns Hopkins University School of Medicine, Baltimore, United States.
Elife ; 122024 Mar 18.
Article in En | MEDLINE | ID: mdl-38497611
ABSTRACT
Eukaryotic gene expression is linked to chromatin structure and nucleosome positioning by ATP-dependent chromatin remodelers that establish and maintain nucleosome-depleted regions (NDRs) near transcription start sites. Conserved yeast RSC and ISW2 remodelers exert antagonistic effects on nucleosomes flanking NDRs, but the temporal dynamics of remodeler search, engagement, and directional nucleosome mobilization for promoter accessibility are unknown. Using optical tweezers and two-color single-particle imaging, we investigated the Brownian diffusion of RSC and ISW2 on free DNA and sparse nucleosome arrays. RSC and ISW2 rapidly scan DNA by one-dimensional hopping and sliding, respectively, with dynamic collisions between remodelers followed by recoil or apparent co-diffusion. Static nucleosomes block remodeler diffusion resulting in remodeler recoil or sequestration. Remarkably, both RSC and ISW2 use ATP hydrolysis to translocate mono-nucleosomes processively at ~30 bp/s on extended linear DNA under tension. Processivity and opposing push-pull directionalities of nucleosome translocation shown by RSC and ISW2 shape the distinctive landscape of promoter chromatin.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Chromatin / Nucleosomes Language: En Journal: Elife Year: 2024 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Chromatin / Nucleosomes Language: En Journal: Elife Year: 2024 Document type: Article Affiliation country: