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Nucleosomes influence multiple steps during replication initiation.

Ishara F Azmi | Shinya Watanabe | Michael F Maloney | Sukhyun Kang | Jason A Belsky | David M MacAlpine | Craig L Peterson | Stephen P Bell
eLife | 2017

Eukaryotic replication origin licensing, activation and timing are influenced by chromatin but a mechanistic understanding is lacking. Using reconstituted nucleosomal DNA replication assays, we assessed the impact of nucleosomes on replication initiation. To generate distinct nucleosomal landscapes, different chromatin-remodeling enzymes (CREs) were used to remodel nucleosomes on origin-DNA templates. Nucleosomal organization influenced two steps of replication initiation: origin licensing and helicase activation. Origin licensing assays showed that local nucleosome positioning enhanced origin specificity and modulated helicase loading by influencing ORC DNA binding. Interestingly, SWI/SNF- and RSC-remodeled nucleosomes were permissive for origin licensing but showed reduced helicase activation. Specific CREs rescued replication of these templates if added prior to helicase activation, indicating a permissive chromatin state must be established during origin licensing to allow efficient origin activation. Our studies show nucleosomes directly modulate origin licensing and activation through distinct mechanisms and provide insights into the regulation of replication initiation by chromatin.

Pubmed ID: 28322723

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Associated grants

  • Agency: NIGMS NIH HHS, United States
    Id: R01 GM054096
  • Agency: NIGMS NIH HHS, United States
    Id: R01 GM104097
  • Agency: NCI NIH HHS, United States
    Id: P30 CA014051
  • Agency: NIGMS NIH HHS, United States
    Id: R35 GM122519
  • Agency: NIGMS NIH HHS, United States
    Id: T32 GM071340

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Bowtie (tool)

RRID:SCR_005476

Software ultrafast memory efficient tool for aligning sequencing reads. Bowtie is short read aligner.

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