4.8 Article

Human Rev1 polymerase disrupts G-quadruplex DNA

Journal

NUCLEIC ACIDS RESEARCH
Volume 42, Issue 5, Pages 3272-3285

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/nar/gkt1314

Keywords

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Funding

  1. U.S.P.H. service [R00 GM084460]
  2. NRF from MEST Korea [2012R1A1A2042391]
  3. Arkansas Breast Cancer Research Program
  4. University of Arkansas for Medical Sciences Translational Research Institute (CTSA Award [UL1TR000039]
  5. UAMS, College of Medicine
  6. National Research Foundation of Korea [2012R1A1A2042391] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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The Y-family DNA polymerase Rev1 is required for successful replication of G-quadruplex DNA (G4 DNA) in higher eukaryotes. Here we show that human Rev1 (hRev1) disrupts G4 DNA structures and prevents refolding in vitro. Nucleotidyl transfer by hRev1 is not necessary for mechanical unfolding to occur. hRev1 binds G4 DNA substrates with K-d,K-DNA values that are 4-15-fold lower than those of non-G4 DNA substrates. The pre-steady-state rate constant of deoxycytidine monophosphate (dCMP) insertion opposite the first tetrad-guanine by hRev1 is similar to 56% as fast as that observed for non-G4 DNA substrates. Thus, hRev1 can promote fork progression by either dislodging tetrad guanines to unfold the G4 DNA, which could assist in extension by other DNA polymerases, or hRev1 can prevent refolding of G4 DNA structures. The hRev1 mechanism of action against G-quadruplexes helps explain why replication progress is impeded at G4 DNA sites in Rev1-deficient cells and illustrates another unique feature of this enzyme with important implications for genome maintenance.

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