4.5 Article

Evidence suggesting that Pif1 helicase functions in DNA replication with the DNA2 helicase/nuclease and DNA polymerase δ

Journal

MOLECULAR AND CELLULAR BIOLOGY
Volume 26, Issue 7, Pages 2490-2500

Publisher

AMER SOC MICROBIOLOGY
DOI: 10.1128/MCB.26.7.2490-2500.2006

Keywords

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Funding

  1. Intramural NIH HHS Funding Source: Medline
  2. NIGMS NIH HHS [GM25508, R01 GM025508] Funding Source: Medline

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The precise machineries required for two aspects of eukaryotic DNA replication, Okazaki fragment processing (OFP) and telomere maintenance, are poorly understood. In this work, we present evidence that Saccharomyces cerevisiae Pif1 helicase plays a wider role in DNA replication than previously appreciated and that it likely functions in conjunction with Dna2 helicase/nuclease as a component of the OFP machinery. In addition, we show that Dna2, which is known to associate with telomeres in a cell-cycle-specific manner, may be a new component of the telomere replication apparatus. Specifically, we show that deletion of PIF1 suppresses the lethality of a DNA2-null mutant. The pif1 Delta dna2 Delta strain remains methylmethane sulfonate sensitive and temperature sensitive; however, these phenotypes can be suppressed by further deletion of a subunit of poll delta, POL32. Deletion of PIF1 also suppresses the cold-sensitive lethality and hydroxyurea sensitivity of the pol32 Delta strain. Dna2 is thought to function by cleaving long flaps that arise during OFP due to excessive strand displacement by pol delta and/or by an as yet unidentified helicase. Thus, suppression of dna2 Delta can be rationalized if deletion of POL32 and/or PIF1 results in a reduction in long flaps that require Dna2 for processing. We further show that deletion of DNA2 suppresses the long-telomere phenotype and the high rate of formation of gross chromosomal rearrangements in pif1 Delta mutants, suggesting a role for Dna2 in telomere elongation in the absence of Pif1.

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