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Structural Studies of Overlapping Dinucleosomes in Solution.
Matsumoto, Atsushi; Sugiyama, Masaaki; Li, Zhenhai; Martel, Anne; Porcar, Lionel; Inoue, Rintaro; Kato, Daiki; Osakabe, Akihisa; Kurumizaka, Hitoshi; Kono, Hidetoshi.
Afiliação
  • Matsumoto A; Institute for Quantum Life Science, National Institutes for Quantum and Radiological Science and Technology, Kizugawa, Japan.
  • Sugiyama M; Institute for Integrated Radiation and Nuclear Science, Kyoto University, Kumatori, Japan. Electronic address: sugiyama@rri.kyoto-u.ac.jp.
  • Li Z; Institute for Quantum Life Science, National Institutes for Quantum and Radiological Science and Technology, Kizugawa, Japan.
  • Martel A; Institut Laue-Langevin, Grenoble, France.
  • Porcar L; Institut Laue-Langevin, Grenoble, France.
  • Inoue R; Institute for Integrated Radiation and Nuclear Science, Kyoto University, Kumatori, Japan.
  • Kato D; Graduate School of Advanced Science & Engineering, Waseda University, Tokyo, Japan.
  • Osakabe A; Graduate School of Advanced Science & Engineering, Waseda University, Tokyo, Japan.
  • Kurumizaka H; Graduate School of Advanced Science & Engineering, Waseda University, Tokyo, Japan; Laboratory of Chromatin Structure and Function, Institute for Quantitative Biosciences, The University of Tokyo, Tokyo, Japan. Electronic address: kurumizaka@iam.u-tokyo.ac.jp.
  • Kono H; Institute for Quantum Life Science, National Institutes for Quantum and Radiological Science and Technology, Kizugawa, Japan. Electronic address: kono.hidetoshi@qst.go.jp.
Biophys J ; 118(9): 2209-2219, 2020 05 05.
Article em En | MEDLINE | ID: mdl-31952809
An overlapping dinucleosome (OLDN) is a structure composed of one hexasome and one octasome and appears to be formed through nucleosome collision promoted by nucleosome remodeling factor(s). In this study, the solution structure of the OLDN was investigated through the integration of small-angle x-ray and neutron scattering (SAXS and SANS, respectively), computer modeling, and molecular dynamics simulations. Starting from the crystal structure, we generated a conformational ensemble based on normal mode analysis and searched for the conformations that reproduced the SAXS and SANS scattering curves well. We found that inclusion of histone tails, which are not observed in the crystal structure, greatly improved model quality. The obtained structural models suggest that OLDNs adopt a variety of conformations stabilized by histone tails situated at the interface between the hexasome and octasome, simultaneously binding to both the hexasomal and octasomal DNA. In addition, our models define a possible direction for the conformational changes or dynamics, which may provide important information that furthers our understanding of the role of chromatin dynamics in gene regulation.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Histonas / Nucleossomos Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Histonas / Nucleossomos Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2020 Tipo de documento: Article