Proliferating Cell Nuclear Antigen (PCNA) May Function as a Double Homotrimer Complex in the Mammalian Cell
The diverse function of proliferating cell nuclear antigen (PCNA) may be regulated by interactions with different protein partners. Interestingly, the binding sites for all known PCNA-associating proteins are on the outer surface or the C termini (“front”) sides of the PCNA trimer. Using cell extrac...
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Veröffentlicht in: | The Journal of biological chemistry 2005-04, Vol.280 (14), p.13888-13894 |
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description | The diverse function of proliferating cell nuclear antigen (PCNA) may be regulated by interactions with different protein partners. Interestingly, the binding sites for all known PCNA-associating proteins are on the outer surface or the C termini (“front”) sides of the PCNA trimer. Using cell extracts and purified human PCNA protein, we show here that two PCNA homotrimers form a back-to-back doublet. Mutation analysis suggests that the Arg-5 and Lys-110 residues on the PCNA back side are the contact points of the two homotrimers in the doublet. Furthermore, short synthetic peptides encompassing either Arg-5 or Lys-110 inhibit double trimer formation. We also found that a PCNA double trimer, but not a homotrimer alone, can simultaneously accommodate chromatin assembly factor-1 and polymerase δ. Together, our data supports a model that chromatin remodeling by chromatin assembly factor-1 (and, possibly, many other cellular activities) are tightly coupled with DNA replication (and repair) through a PCNA double trimer complex. |
doi_str_mv | 10.1074/jbc.M500304200 |
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Interestingly, the binding sites for all known PCNA-associating proteins are on the outer surface or the C termini (“front”) sides of the PCNA trimer. Using cell extracts and purified human PCNA protein, we show here that two PCNA homotrimers form a back-to-back doublet. Mutation analysis suggests that the Arg-5 and Lys-110 residues on the PCNA back side are the contact points of the two homotrimers in the doublet. Furthermore, short synthetic peptides encompassing either Arg-5 or Lys-110 inhibit double trimer formation. We also found that a PCNA double trimer, but not a homotrimer alone, can simultaneously accommodate chromatin assembly factor-1 and polymerase δ. 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Interestingly, the binding sites for all known PCNA-associating proteins are on the outer surface or the C termini (“front”) sides of the PCNA trimer. Using cell extracts and purified human PCNA protein, we show here that two PCNA homotrimers form a back-to-back doublet. Mutation analysis suggests that the Arg-5 and Lys-110 residues on the PCNA back side are the contact points of the two homotrimers in the doublet. Furthermore, short synthetic peptides encompassing either Arg-5 or Lys-110 inhibit double trimer formation. We also found that a PCNA double trimer, but not a homotrimer alone, can simultaneously accommodate chromatin assembly factor-1 and polymerase δ. Together, our data supports a model that chromatin remodeling by chromatin assembly factor-1 (and, possibly, many other cellular activities) are tightly coupled with DNA replication (and repair) through a PCNA double trimer complex.</description><subject>Animals</subject><subject>Arginine - metabolism</subject><subject>CHO Cells</subject><subject>Chromatin - metabolism</subject><subject>Cricetinae</subject><subject>DNA - metabolism</subject><subject>DNA Mutational Analysis</subject><subject>Humans</subject><subject>Lysine - metabolism</subject><subject>Macromolecular Substances</subject><subject>Models, Molecular</subject><subject>Peptides - genetics</subject><subject>Peptides - metabolism</subject><subject>Proliferating Cell Nuclear Antigen - chemistry</subject><subject>Proliferating Cell Nuclear Antigen - genetics</subject><subject>Proliferating Cell Nuclear Antigen - metabolism</subject><subject>Protein Structure, Quaternary</subject><subject>Protein Structure, Tertiary</subject><subject>Recombinant Fusion Proteins - chemistry</subject><subject>Recombinant Fusion Proteins - genetics</subject><subject>Recombinant Fusion Proteins - metabolism</subject><issn>0021-9258</issn><issn>1083-351X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUFv1DAQhS0EokvhyhH5gBAcsngcO3aOq0ApUlt6AImb5TiTXZck3toJ0H-P6a7UE8LSyJfvPb2ZR8hLYGtgSry_ad36UjJWMsEZe0RWwHRZlBK-PyYrxjgUNZf6hDxL6YblJ2p4Sk5AaiYB1Ir8uI5h8D1GO_tpSxscBnq1uAFtpJtp9luc6Nvr5mrzjl7aO3q2TG72YaI2UUs_hKUdkJ6HMczRjxhpE8b9gL-pn-i8wywZRzt4O90bPydPejskfHH8T8m3s49fm_Pi4sunz83monBC8LkAjihkBa2SZdnKvhVCKlRdXdWVcKJmVQcc8lhrVY91XlCh7TRA1aqKufKUvDn47mO4XTDNZvTJ5QB2wrAkU6nsxLT-LwhKK645ZHB9AF0MKUXszT7va-OdAWb-9mByD-ahhyx4dXRe2hG7B_x4-Ay8PgA7v9398hFN64Pb4Wi4zpbCQKnvE-oDhvlePz1Gk5zHyWGXJW42XfD_ivAHJuagMA</recordid><startdate>20050408</startdate><enddate>20050408</enddate><creator>Naryzhny, Stanislav N.</creator><creator>Zhao, Helen</creator><creator>Lee, Hoyun</creator><general>Elsevier Inc</general><general>American Society for Biochemistry and Molecular Biology</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TM</scope><scope>7X8</scope></search><sort><creationdate>20050408</creationdate><title>Proliferating Cell Nuclear Antigen (PCNA) May Function as a Double Homotrimer Complex in the Mammalian Cell</title><author>Naryzhny, Stanislav N. ; Zhao, Helen ; Lee, Hoyun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c442t-12ee4561b7533b5fb4457e7d96964c4906d121d12aaa7fe99257ead8116b760c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Animals</topic><topic>Arginine - metabolism</topic><topic>CHO Cells</topic><topic>Chromatin - metabolism</topic><topic>Cricetinae</topic><topic>DNA - metabolism</topic><topic>DNA Mutational Analysis</topic><topic>Humans</topic><topic>Lysine - metabolism</topic><topic>Macromolecular Substances</topic><topic>Models, Molecular</topic><topic>Peptides - genetics</topic><topic>Peptides - metabolism</topic><topic>Proliferating Cell Nuclear Antigen - chemistry</topic><topic>Proliferating Cell Nuclear Antigen - genetics</topic><topic>Proliferating Cell Nuclear Antigen - metabolism</topic><topic>Protein Structure, Quaternary</topic><topic>Protein Structure, Tertiary</topic><topic>Recombinant Fusion Proteins - chemistry</topic><topic>Recombinant Fusion Proteins - genetics</topic><topic>Recombinant Fusion Proteins - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Naryzhny, Stanislav N.</creatorcontrib><creatorcontrib>Zhao, Helen</creatorcontrib><creatorcontrib>Lee, Hoyun</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Nucleic Acids Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of biological chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Naryzhny, Stanislav N.</au><au>Zhao, Helen</au><au>Lee, Hoyun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Proliferating Cell Nuclear Antigen (PCNA) May Function as a Double Homotrimer Complex in the Mammalian Cell</atitle><jtitle>The Journal of biological chemistry</jtitle><addtitle>J Biol Chem</addtitle><date>2005-04-08</date><risdate>2005</risdate><volume>280</volume><issue>14</issue><spage>13888</spage><epage>13894</epage><pages>13888-13894</pages><issn>0021-9258</issn><eissn>1083-351X</eissn><abstract>The diverse function of proliferating cell nuclear antigen (PCNA) may be regulated by interactions with different protein partners. Interestingly, the binding sites for all known PCNA-associating proteins are on the outer surface or the C termini (“front”) sides of the PCNA trimer. Using cell extracts and purified human PCNA protein, we show here that two PCNA homotrimers form a back-to-back doublet. Mutation analysis suggests that the Arg-5 and Lys-110 residues on the PCNA back side are the contact points of the two homotrimers in the doublet. Furthermore, short synthetic peptides encompassing either Arg-5 or Lys-110 inhibit double trimer formation. We also found that a PCNA double trimer, but not a homotrimer alone, can simultaneously accommodate chromatin assembly factor-1 and polymerase δ. 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subjects | Animals Arginine - metabolism CHO Cells Chromatin - metabolism Cricetinae DNA - metabolism DNA Mutational Analysis Humans Lysine - metabolism Macromolecular Substances Models, Molecular Peptides - genetics Peptides - metabolism Proliferating Cell Nuclear Antigen - chemistry Proliferating Cell Nuclear Antigen - genetics Proliferating Cell Nuclear Antigen - metabolism Protein Structure, Quaternary Protein Structure, Tertiary Recombinant Fusion Proteins - chemistry Recombinant Fusion Proteins - genetics Recombinant Fusion Proteins - metabolism |
title | Proliferating Cell Nuclear Antigen (PCNA) May Function as a Double Homotrimer Complex in the Mammalian Cell |
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