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The Chd1 Chromatin Remodeler Shifts Nucleosomal DNA Bidirectionally as a Monomer.
Qiu, Yupeng; Levendosky, Robert F; Chakravarthy, Srinivas; Patel, Ashok; Bowman, Gregory D; Myong, Sua.
Affiliation
  • Qiu Y; Department of Biophysics, Johns Hopkins University, Baltimore, MD 21218, USA; Department of Bioengineering, University of Illinois, Urbana, IL 61801, USA.
  • Levendosky RF; Department of Biophysics, Johns Hopkins University, Baltimore, MD 21218, USA.
  • Chakravarthy S; Biophysics Collaborative Access Team, Argonne National Laboratory, Argonne, IL 60439, USA.
  • Patel A; Kusuma School of Biological Sciences, Indian Institute of Technology Delhi, Hauz Khas, New Delhi 110016, India.
  • Bowman GD; Department of Biophysics, Johns Hopkins University, Baltimore, MD 21218, USA. Electronic address: gdbowman@jhu.edu.
  • Myong S; Department of Biophysics, Johns Hopkins University, Baltimore, MD 21218, USA; Department of Bioengineering, University of Illinois, Urbana, IL 61801, USA; Physics Frontier Center (Center for Physics of Living Cells), University of Illinois, Urbana, IL 61801, USA. Electronic address: smyong@jhu.edu.
Mol Cell ; 68(1): 76-88.e6, 2017 Oct 05.
Article in En | MEDLINE | ID: mdl-28943314
ABSTRACT
Chromatin remodelers catalyze dynamic packaging of the genome by carrying out nucleosome assembly/disassembly, histone exchange, and nucleosome repositioning. Remodeling results in evenly spaced nucleosomes, which requires probing both sides of the nucleosome, yet the way remodelers organize sliding activity to achieve this task is not understood. Here, we show that the monomeric Chd1 remodeler shifts DNA back and forth by dynamically alternating between different segments of the nucleosome. During sliding, Chd1 generates unstable remodeling intermediates that spontaneously relax to a pre-remodeled position. We demonstrate that nucleosome sliding is tightly controlled by two regulatory domains the DNA-binding domain, which interferes with sliding when its range is limited by a truncated linking segment, and the chromodomains, which play a key role in substrate discrimination. We propose that active interplay of the ATPase motor with the regulatory domains may promote dynamic nucleosome structures uniquely suited for histone exchange and chromatin reorganization during transcription.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Saccharomyces cerevisiae / Transcription, Genetic / DNA / Histones / Nucleosomes / Saccharomyces cerevisiae Proteins / DNA-Binding Proteins Language: En Journal: Mol Cell Journal subject: BIOLOGIA MOLECULAR Year: 2017 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Saccharomyces cerevisiae / Transcription, Genetic / DNA / Histones / Nucleosomes / Saccharomyces cerevisiae Proteins / DNA-Binding Proteins Language: En Journal: Mol Cell Journal subject: BIOLOGIA MOLECULAR Year: 2017 Type: Article Affiliation country: United States