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Saccharomyces cerevisiae DNA Polymerase ε and Polymerase σ Interact Physically and Functionally, Suggesting a Role for Polymerase ε in Sister Chromatid Cohesion

Edwards, Shaune and Li, Caroline M. and Levy, Daniel L. and Brown, Jessica and Snow, Peter M. and Campbell, Judith L. (2003) Saccharomyces cerevisiae DNA Polymerase ε and Polymerase σ Interact Physically and Functionally, Suggesting a Role for Polymerase ε in Sister Chromatid Cohesion. Molecular and Cellular Biology, 23 (8). pp. 2733-2748. ISSN 0270-7306. http://resolver.caltech.edu/CaltechAUTHORS:20111011-085516908

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Abstract

The large subunit of Saccharomyces cerevisiae DNA polymerase ε, Pol2, comprises two essential functions. The N terminus has essential DNA polymerase activity. The C terminus is also essential, but its function is unknown. We report here that the C-terminal domain of Pol2 interacts with polymerase σ (Pol σ), a recently identified, essential nuclear nucleotidyl transferase encoded by two redundant genes, TRF4 and TRF5. This interaction is functional, since Pol σ stimulates the polymerase activity of the Pol ε holoenzyme significantly. Since Trf4 is required for sister chromatid cohesion as well as for completion of S phase and repair, the interaction suggested that Pol ε, like Pol σ, might form a link between the replication apparatus and sister chromatid cohesion and/or repair machinery. We present evidence that pol2 mutants are defective in sister chromatid cohesion. In addition, Pol2 interacts with SMC1, a subunit of the cohesin complex, and with ECO1/CTF7, required for establishing sister chromatid cohesion; and pol2 mutations act synergistically with smc1 and scc1. We also show that trf5∆ mutants, like trf4∆ mutants, are defective in DNA repair and sister chromatid cohesion.


Item Type:Article
Related URLs:
URLURL TypeDescription
http://dx.doi.org/10.1128/MCB.23.8.2733-2748.2003DOIUNSPECIFIED
http://mcb.asm.org/cgi/content/abstract/23/8/2733PublisherUNSPECIFIED
Additional Information:© 2003 American Society for Microbiology. Received 16 August 2002; Returned for modification 25 September 2002; Accepted 16 January 2003. We are grateful to Michael Christman and members of his laboratory for strains, plasmids, and valuable advice. We thank R. D. Deshaies and G. Alexandru for comments on the manuscript and Ray Deshaies for the use of his microscope. This work was supported by PHS GM25508. S. Edwards was supported by a PHS Research Supplement for Underrepresented Minorities.
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Funding AgencyGrant Number
PHSGM25508
PHS Research Supplement for Underrepresented MinoritiesUNSPECIFIED
Record Number:CaltechAUTHORS:20111011-085516908
Persistent URL:http://resolver.caltech.edu/CaltechAUTHORS:20111011-085516908
Usage Policy:No commercial reproduction, distribution, display or performance rights in this work are provided.
ID Code:27153
Collection:CaltechAUTHORS
Deposited By: Tony Diaz
Deposited On:14 Oct 2011 17:18
Last Modified:14 Oct 2011 17:18

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