| Title |
Evidence that DNA polymerase δ contributes to initiating leading strand DNA replication in Saccharomyces cerevisiae
|
|---|---|
| Published in |
Nature Communications, February 2018
|
| DOI | 10.1038/s41467-018-03270-4 |
| Pubmed ID | |
| Authors | |
| Abstract |
To investigate nuclear DNA replication enzymology in vivo, we have studied Saccharomyces cerevisiae strains containing a pol2-16 mutation that inactivates the catalytic activities of DNA polymerase ε (Pol ε). Although pol2-16 mutants survive, they present very tiny spore colonies, increased doubling time, larger than normal cells, aberrant nuclei, and rapid acquisition of suppressor mutations. These phenotypes reveal a severe growth defect that is distinct from that of strains that lack only Pol ε proofreading (pol2-4), consistent with the idea that Pol ε is the major leading-strand polymerase used for unstressed DNA replication. Ribonucleotides are incorporated into the pol2-16 genome in patterns consistent with leading-strand replication by Pol δ when Pol ε is absent. More importantly, ribonucleotide distributions at replication origins suggest that in strains encoding all three replicases, Pol δ contributes to initiation of leading-strand replication. We describe two possible models. |
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Demographic breakdown
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Mendeley demographics
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Demographic breakdown
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| Researcher | 15 | 14% |
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| Student > Master | 12 | 11% |
| Professor | 6 | 6% |
| Other | 13 | 12% |
| Unknown | 21 | 20% |
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| Pharmacology, Toxicology and Pharmaceutical Science | 1 | <1% |
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