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An Alternative Pathway for Okazaki Fragment Processing - Resolution of Fold-Back Flaps by Pif1 Helicase

Pike, Jason E. and Henry, Ryan A. and Burgers, Peter M. J. and Campbell, Judith L. and Bambara, Robert A. (2010) An Alternative Pathway for Okazaki Fragment Processing - Resolution of Fold-Back Flaps by Pif1 Helicase. Journal of Biological Chemistry, 285 (53). pp. 41712-41723. ISSN 0021-9258. PMCID PMC3009898. https://resolver.caltech.edu/CaltechAUTHORS:20110301-110042696

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Abstract

Two pathways have been proposed for eukaryotic Okazaki fragment RNA primer removal. Results presented here provide evidence for an alternative pathway. Primer extension by DNA polymerase δ (pol δ) displaces the downstream fragment into an RNA-initiated flap. Most flaps are cleaved by flap endonuclease 1 (FEN1) while short, and the remaining nicks joined in the first pathway. A small fraction escapes immediate FEN1 cleavage and is further lengthened by Pif1 helicase. Long flaps are bound by replication protein A (RPA), which inhibits FEN1. In the second pathway, Dna2 nuclease cleaves an RPA-bound flap and displaces RPA, leaving a short flap for FEN1. Pif1 flap lengthening creates a requirement for Dna2. This relationship should not have evolved unless Pif1 had an important role in fragment processing. In this study, biochemical reconstitution experiments were used to gain insight into this role. Pif1 did not promote synthesis through GC-rich sequences, which impede strand displacement. Pif1 was also unable to open fold-back flaps that are immune to cleavage by either FEN1 or Dna2 and cannot be bound by RPA. However, Pif1 working with pol δ readily unwound a full-length Okazaki fragment initiated by a fold-back flap. Additionally, a fold-back in the template slowed pol δ synthesis, so that the fragment could be removed before ligation to the lagging strand. These results suggest an alternative pathway in which Pif1 removes Okazaki fragments initiated by fold-back flaps in vivo.


Item Type:Article
Related URLs:
URLURL TypeDescription
http://dx.doi.org/10.1074/jbc.M110.146894 DOIArticle
http://www.jbc.org/content/285/53/41712PublisherArticle
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3009898/PubMed CentralArticle
Additional Information:© 2010 by The American Society for Biochemistry and Molecular Biology, Inc. Received for publication,May 20, 2010, and in revised form, October 13, 2010. First Published on October 19, 2010. This work was supported, in whole or in part, by National Institutes of Health Grants GM024441 (to R. A. B.), GM078666 (to J. L. C.), and GM032431 (to P. M. J. B.). We thank the members of the Bambara laboratory for helpful discussions and suggestions. We thank Dr. Marc Wold for providing us with purified RPA.
Funders:
Funding AgencyGrant Number
NIHGM024441
NIHGM078666
NIHGM032431
Issue or Number:53
PubMed Central ID:PMC3009898
Record Number:CaltechAUTHORS:20110301-110042696
Persistent URL:https://resolver.caltech.edu/CaltechAUTHORS:20110301-110042696
Usage Policy:No commercial reproduction, distribution, display or performance rights in this work are provided.
ID Code:22575
Collection:CaltechAUTHORS
Deposited By: Tony Diaz
Deposited On:03 Mar 2011 17:17
Last Modified:03 Oct 2019 02:38

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