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Cell-Cycle Regulation of Dynamic Chromosome Association of the Condensin Complex.
Thadani, Rahul; Kamenz, Julia; Heeger, Sebastian; Muñoz, Sofía; Uhlmann, Frank.
Afiliação
  • Thadani R; Chromosome Segregation Laboratory, The Francis Crick Institute, London NW1 1AT, UK; Laboratory of Biochemistry and Molecular Biology, National Cancer Institute, NIH, Bethesda, MD 20892, USA.
  • Kamenz J; Chromosome Segregation Laboratory, The Francis Crick Institute, London NW1 1AT, UK.
  • Heeger S; Chromosome Segregation Laboratory, The Francis Crick Institute, London NW1 1AT, UK.
  • Muñoz S; Chromosome Segregation Laboratory, The Francis Crick Institute, London NW1 1AT, UK.
  • Uhlmann F; Chromosome Segregation Laboratory, The Francis Crick Institute, London NW1 1AT, UK. Electronic address: frank.uhlmann@crick.ac.uk.
Cell Rep ; 23(8): 2308-2317, 2018 05 22.
Article em En | MEDLINE | ID: mdl-29791843
ABSTRACT
Eukaryotic cells inherit their genomes in the form of chromosomes, which are formed from the compaction of interphase chromatin by the condensin complex. Condensin is a member of the structural maintenance of chromosomes (SMC) family of ATPases, large ring-shaped protein assemblies that entrap DNA to establish chromosomal interactions. Here, we use the budding yeast Saccharomyces cerevisiae to dissect the role of the condensin ATPase and its relationship with cell-cycle-regulated chromosome binding dynamics. ATP hydrolysis-deficient condensin binds to chromosomes but is defective in chromosome condensation and segregation. By modulating the ATPase, we demonstrate that it controls condensin's dynamic turnover on chromosomes. Mitosis-specific phosphorylation of condensin's Smc4 subunit reduces the turnover rate. However, reducing turnover by itself is insufficient to compact chromosomes. We propose that condensation requires fine-tuned dynamic condensin interactions with more than one DNA. These results enhance our molecular understanding of condensin function during chromosome condensation.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Saccharomyces cerevisiae / Cromossomos Fúngicos / Ciclo Celular / Adenosina Trifosfatases / Complexos Multiproteicos / Proteínas de Ligação a DNA Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Saccharomyces cerevisiae / Cromossomos Fúngicos / Ciclo Celular / Adenosina Trifosfatases / Complexos Multiproteicos / Proteínas de Ligação a DNA Idioma: En Ano de publicação: 2018 Tipo de documento: Article