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Components of the Secondary Pathway Stimulate the Primary Pathway of Eukaryotic Okazaki Fragment Processing

Henry, Ryan A. and Balakrishnan, Lata and Ying-Lin, Stefanie Tan and Campbell, Judith L. and Bambara, Robert A. (2010) Components of the Secondary Pathway Stimulate the Primary Pathway of Eukaryotic Okazaki Fragment Processing. Journal of Biological Chemistry, 285 (37). 28496-28505 . ISSN 0021-9258. PMCID PMC2937875.

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Reconstitution of eukaryotic Okazaki fragment processing implicates both one- and two-nuclease pathways for processing flap intermediates. In most cases, FEN1 (flap endonuclease 1) is able to efficiently cleave short flaps as they form. However, flaps escaping cleavage bind replication protein A (RPA) inhibiting FEN1. The flaps must then be cleaved by Dna2 nuclease/helicase before FEN1 can act. Pif1 helicase aids creation of long flaps. The pathways were considered connected only in that the products of Dna2 cleavage are substrates for FEN1. However, results presented here show that Dna2, Pif1, and RPA, the unique proteins of the two-nuclease pathway from Saccharomyces cerevisiae, all stimulate FEN1 acting in the one-nuclease pathway. Stimulation is observed on RNA flaps representing the initial displacement and on short DNA flaps, subsequently displaced. Neither the RNA nor the short DNA flaps can bind the two-nuclease pathway proteins. Instead, direct interactions between FEN1 and the two-nuclease pathway proteins have been detected. These results suggest that the proteins are either part of a complex or interact successively with FEN1 because the level of stimulation would be similar either way. Proteins bound to FEN1 could be tethered to the flap base by the interaction of FEN1 with PCNA, potentially improving their availability when flaps become long. These findings also support a model in which cleavage by FEN1 alone is the preferred pathway, with the first opportunity to complete cleavage, and is stimulated by components of the backup pathway.

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Additional Information:© 2010 The American Society for Biochemistry and Molecular Biology, Inc. Received for publication, April 8, 2010, and in revised form, July 6, 2010. Published, JBC Papers in Press, July 13, 2010. This work was supported, in whole or in part, by National Institutes of Health Grants GM024441 (to R. A. B.) and GM087666 (to J. L. C.). We thank the members of the Bambara laboratory for helpful discussions and suggestions. We thank Dr. Marc Wold for providing purified RPA.
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Issue or Number:37
PubMed Central ID:PMC2937875
Record Number:CaltechAUTHORS:20100928-100850545
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Usage Policy:No commercial reproduction, distribution, display or performance rights in this work are provided.
ID Code:20179
Deposited By: Tony Diaz
Deposited On:28 Sep 2010 19:59
Last Modified:03 Oct 2019 02:06

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