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Identification of Elg1 interaction partners and effects on post-replication chromatin re-formation
Author(s) -
Vamsi K. Gali,
David Dickerson,
Yuki Katou,
Katsunori Fujiki,
Katsuhiko Shirahige,
Tom OwenHughes,
Takashi Kubota,
Anne D. Donaldson
Publication year - 2018
Publication title -
plos genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.587
H-Index - 233
eISSN - 1553-7404
pISSN - 1553-7390
DOI - 10.1371/journal.pgen.1007783
Subject(s) - biology , dna replication factor cdt1 , origin recognition complex , control of chromosome duplication , licensing factor , replication factor c , dna replication , chromatin , eukaryotic dna replication , pre replication complex , genetics , nucleosome , proliferating cell nuclear antigen , replication protein a , microbiology and biotechnology , dna , dna binding protein , transcription factor , gene
Elg1, the major subunit of a Replication Factor C-like complex, is critical to ensure genomic stability during DNA replication, and is implicated in controlling chromatin structure. We investigated the consequences of Elg1 loss for the dynamics of chromatin re-formation following DNA replication. Measurement of Okazaki fragment length and the micrococcal nuclease sensitivity of newly replicated DNA revealed a defect in nucleosome organization in the absence of Elg1. Using a proteomic approach to identify Elg1 binding partners, we discovered that Elg1 interacts with Rtt106, a histone chaperone implicated in replication-coupled nucleosome assembly that also regulates transcription. A central role for Elg1 is the unloading of PCNA from chromatin following DNA replication, so we examined the relative importance of Rtt106 and PCNA unloading for chromatin reassembly following DNA replication. We find that the major cause of the chromatin organization defects of an ELG1 mutant is PCNA retention on DNA following replication, with Rtt106-Elg1 interaction potentially playing a contributory role.

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