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Elasticity control of entangled chromosomes: Crosstalk between condensin complexes and nucleosomes.
Yamamoto, Tetsuya; Kinoshita, Kazuhisa; Hirano, Tatsuya.
Afiliación
  • Yamamoto T; Institute for Chemical Reaction Design and Discovery (ICReDD), Hokkaido University, Sapporo, Hokkaido, Japan. Electronic address: tyamamoto@icredd.hokudai.ac.jp.
  • Kinoshita K; Chromosome Dynamics Laboratory, RIKEN, Wako, Saitama, Japan.
  • Hirano T; Chromosome Dynamics Laboratory, RIKEN, Wako, Saitama, Japan.
Biophys J ; 122(19): 3869-3881, 2023 10 03.
Article en En | MEDLINE | ID: mdl-37571823
ABSTRACT
Condensin-mediated loop extrusion is now considered as the main driving force of mitotic chromosome assembly. Recent experiments have shown, however, that a class of mutant condensin complexes deficient in loop extrusion can assemble chromosome-like structures in Xenopus egg extracts, although these structures are somewhat different from those assembled by wild-type condensin complexes. In the absence of topoisomerase II (topo II), the mutant condensin complexes produce an unusual round-shaped structure termed a bean, which consists of a DNA-dense central core surrounded by a DNA-sparse halo. The mutant condensin complexes accumulate in the core, whereas histones are more concentrated in the halo than in the core. We consider that this peculiar structure serves as a model system to study how DNA entanglements, nucleosomes, and condensin functionally crosstalk with each other. To gain insight into how the bean structure is formed, here we construct a theoretical model. Our theory predicts that the core is formed by attractive interactions between mutant condensin complexes, whereas the halo is stabilized by the energy reduction through the selective accumulation of nucleosomes. The formation of the halo increases the elastic free energy due to the DNA entanglement in the core, but the latter free energy is compensated by condensin complexes that suppress the assembly of nucleosomes.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Nucleosomas / Mitosis Tipo de estudio: Prognostic_studies Idioma: En Revista: Biophys J Año: 2023 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Nucleosomas / Mitosis Tipo de estudio: Prognostic_studies Idioma: En Revista: Biophys J Año: 2023 Tipo del documento: Article