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Dynamic relocalization of replication origins by Fkh1 requires execution of DDK function and Cdc45 loading at origins.
Zhang, Haiyang; Petrie, Meghan V; He, Yiwei; Peace, Jared M; Chiolo, Irene E; Aparicio, Oscar M.
Afiliação
  • Zhang H; Molecular and Computational Biology Section, Department of Biological Sciences, University of Southern California, Los Angeles, United States.
  • Petrie MV; Molecular and Computational Biology Section, Department of Biological Sciences, University of Southern California, Los Angeles, United States.
  • He Y; Molecular and Computational Biology Section, Department of Biological Sciences, University of Southern California, Los Angeles, United States.
  • Peace JM; Molecular and Computational Biology Section, Department of Biological Sciences, University of Southern California, Los Angeles, United States.
  • Chiolo IE; Molecular and Computational Biology Section, Department of Biological Sciences, University of Southern California, Los Angeles, United States.
  • Aparicio OM; Molecular and Computational Biology Section, Department of Biological Sciences, University of Southern California, Los Angeles, United States.
Elife ; 82019 05 14.
Article em En | MEDLINE | ID: mdl-31084713
ABSTRACT
Chromosomal DNA elements are organized into spatial domains within the eukaryotic nucleus. Sites undergoing DNA replication, high-level transcription, and repair of double-strand breaks coalesce into foci, although the significance and mechanisms giving rise to these dynamic structures are poorly understood. In S. cerevisiae, replication origins occupy characteristic subnuclear localizations that anticipate their initiation timing during S phase. Here, we link localization of replication origins in G1 phase with Fkh1 activity, which is required for their early replication timing. Using a Fkh1-dependent origin relocalization assay, we determine that execution of Dbf4-dependent kinase function, including Cdc45 loading, results in dynamic relocalization of a replication origin from the nuclear periphery to the interior in G1 phase. Origin mobility increases substantially with Fkh1-driven relocalization. These findings provide novel molecular insight into the mechanisms that govern dynamics and spatial organization of DNA replication origins and possibly other functional DNA elements.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Saccharomyces cerevisiae / Proteínas Nucleares / Origem de Replicação / Proteínas de Ciclo Celular / Proteínas de Saccharomyces cerevisiae / Proteínas de Ligação a DNA / Fatores de Transcrição Forkhead Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Saccharomyces cerevisiae / Proteínas Nucleares / Origem de Replicação / Proteínas de Ciclo Celular / Proteínas de Saccharomyces cerevisiae / Proteínas de Ligação a DNA / Fatores de Transcrição Forkhead Idioma: En Ano de publicação: 2019 Tipo de documento: Article