PCNA ubiquitylation ensures timely completion of unperturbed DNA replication in fission yeast
Author(s) -
Yasukazu Daigaku,
Thomas J. Etheridge,
Yuka Nakazawa,
Mayumi Nakayama,
Adam T. Watson,
Izumi Miyabe,
Tomoo Ogi,
Mark A. Osborne,
Antony M. Carr
Publication year - 2017
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.1006789
Subject(s) - proliferating cell nuclear antigen , biology , replication factor c , dna replication , ubiquitin , dna polymerase delta , control of chromosome duplication , schizosaccharomyces pombe , okazaki fragments , microbiology and biotechnology , dna polymerase , origin recognition complex , eukaryotic dna replication , dna , genetics , saccharomyces cerevisiae , yeast , polymerase chain reaction , gene , reverse transcriptase
PCNA ubiquitylation on lysine 164 is required for DNA damage tolerance. In many organisms PCNA is also ubiquitylated in unchallenged S phase but the significance of this has not been established. Using Schizosaccharomyces pombe , we demonstrate that lysine 164 ubiquitylation of PCNA contributes to efficient DNA replication in the absence of DNA damage. Loss of PCNA ubiquitylation manifests most strongly at late replicating regions and increases the frequency of replication gaps. We show that PCNA ubiquitylation increases the proportion of chromatin associated PCNA and the co-immunoprecipitation of Polymerase δ with PCNA during unperturbed replication and propose that ubiquitylation acts to prolong the chromatin association of these replication proteins to allow the efficient completion of Okazaki fragment synthesis by mediating gap filling.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom