Ku antigen, an origin-specific binding protein that associates with replication proteins, is required for mammalian DNA replication

Ors binding activity (OBA) represents a HeLa cell protein activity that binds in a sequence-specific manner to A3/4, a 36-bp mammalian replication origin sequence. OBA's DNA binding domain is identical to the 80-kDa subunit of Ku antigen. Ku antigen associates with mammalian origins of DNA repl...

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Veröffentlicht in:Biochimica et biophysica acta 2002-10, Vol.1578 (1), p.59-72
Hauptverfasser: Matheos, Diamanto, Ruiz, Marcia T, Price, Gerald B, Zannis-Hadjopoulos, Maria
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Price, Gerald B
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description Ors binding activity (OBA) represents a HeLa cell protein activity that binds in a sequence-specific manner to A3/4, a 36-bp mammalian replication origin sequence. OBA's DNA binding domain is identical to the 80-kDa subunit of Ku antigen. Ku antigen associates with mammalian origins of DNA replication in vivo, with maximum binding at the G1/S phase. Addition of an A3/4 double-stranded oligonucleotide inhibited in vitro DNA replication of p186, p ors12, and pX24, plasmids containing the monkey replication origins of ors8, ors12, and the Chinese hamster DHFR oriβ, respectively. In contrast, in vitro SV40 DNA replication remained unaffected. The inhibitory effect of A3/4 oligonucleotide was fully reversed upon addition of affinity-purified Ku. Furthermore, depletion of Ku by inclusion of an antibody recognizing the Ku heterodimer, Ku70/Ku80, decreased mammalian replication to basal levels. By co-immunoprecipitation analyses, Ku was found to interact with DNA polymerases α, δ and ε, PCNA, topoisomerase II, RF-C, RP-A, DNA-PKcs, ORC-2, and Oct-1. These interactions were not inhibited by the presence of ethidium bromide in the immunoprecipitation reaction, suggesting DNA-independent protein associations. The data suggest an involvement of Ku in mammalian DNA replication as an origin-specific-binding protein with DNA helicase activity. Ku acts at the initiation step of replication and requires an A3/4-homologous sequence for origin binding. The physical association of Ku with replication proteins reveals a possible mechanism by which Ku is recruited to mammalian origins.
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OBA's DNA binding domain is identical to the 80-kDa subunit of Ku antigen. Ku antigen associates with mammalian origins of DNA replication in vivo, with maximum binding at the G1/S phase. Addition of an A3/4 double-stranded oligonucleotide inhibited in vitro DNA replication of p186, p ors12, and pX24, plasmids containing the monkey replication origins of ors8, ors12, and the Chinese hamster DHFR oriβ, respectively. In contrast, in vitro SV40 DNA replication remained unaffected. The inhibitory effect of A3/4 oligonucleotide was fully reversed upon addition of affinity-purified Ku. Furthermore, depletion of Ku by inclusion of an antibody recognizing the Ku heterodimer, Ku70/Ku80, decreased mammalian replication to basal levels. By co-immunoprecipitation analyses, Ku was found to interact with DNA polymerases α, δ and ε, PCNA, topoisomerase II, RF-C, RP-A, DNA-PKcs, ORC-2, and Oct-1. 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The physical association of Ku with replication proteins reveals a possible mechanism by which Ku is recruited to mammalian origins.</description><subject>Animals</subject><subject>Antibodies - pharmacology</subject><subject>Antigens, Nuclear</subject><subject>Cricetinae</subject><subject>Cricetulus</subject><subject>Deoxyribonucleases, Type II Site-Specific</subject><subject>DHFR origin</subject><subject>DNA Helicases - metabolism</subject><subject>DNA Replication - drug effects</subject><subject>DNA-Binding Proteins - immunology</subject><subject>DNA-Binding Proteins - metabolism</subject><subject>DNA-Binding Proteins - pharmacology</subject><subject>DNA-Directed DNA Polymerase - metabolism</subject><subject>Haplorhini</subject><subject>HeLa Cells</subject><subject>Host Cell Factor C1</subject><subject>Humans</subject><subject>Ku antigen</subject><subject>Ku Autoantigen</subject><subject>Mammalian DNA replication</subject><subject>Nuclear Proteins - immunology</subject><subject>Nuclear Proteins - metabolism</subject><subject>Nuclear Proteins - pharmacology</subject><subject>Octamer Transcription Factor-1</subject><subject>Oligonucleotides - antagonists &amp; inhibitors</subject><subject>Oligonucleotides - pharmacology</subject><subject>Origin of DNA replication</subject><subject>Replication Origin</subject><subject>Replication Protein A</subject><subject>SV40 in vitro replication</subject><subject>Transcription Factors - metabolism</subject><issn>0167-4781</issn><issn>0006-3002</issn><issn>1879-2634</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1PFTEUhhsigSv6EzBdGUkY7Md8tCtCQMBAdKGum07nzOWYmc6l7WhY88ft5V7RHV20zelz-p68LyGHnJ1wxuuP3_LWFGWj-AcmjhgrdVPoHbLgqtGFqGX5iiyekX3yOsafLK-a13tknwupJVdqQR5vZmp9wiX443yhU8Al-iKuwGGPjrboO_RLugpTAvQ03dlEbYyTQ5sg0t-Y7miA1YDOJpz8XzAeU4z54X7GAB3tp0BHO452wCxy8eXs_543ZLe3Q4S32_OA_Lj89P38urj9evX5_Oy2cFKLVLSyL4Wthah51bhOKiZtB0pW3CmtS6F5aRmotpOs72Xbuqpy3JawLmjFrDwg7zf_5hnvZ4jJjBgdDIP1MM3RNKISQmj9Ipg9FozxKoPVBnRhijFAb1YBRxseDGdmHZN5ismsMzBMmKeYzFrg3VZgbkfo_nVtc8nA6QaA7McvhGCiQ_AOumynS6ab8AWJP6rZo9o</recordid><startdate>20021011</startdate><enddate>20021011</enddate><creator>Matheos, Diamanto</creator><creator>Ruiz, Marcia T</creator><creator>Price, Gerald B</creator><creator>Zannis-Hadjopoulos, Maria</creator><general>Elsevier B.V</general><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>20021011</creationdate><title>Ku antigen, an origin-specific binding protein that associates with replication proteins, is required for mammalian DNA replication</title><author>Matheos, Diamanto ; Ruiz, Marcia T ; Price, Gerald B ; Zannis-Hadjopoulos, Maria</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c392t-b3f42a6226157cd3803ade8351c89942914a0e8bd30ff3bbc55c1a4ebd30980a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Animals</topic><topic>Antibodies - pharmacology</topic><topic>Antigens, Nuclear</topic><topic>Cricetinae</topic><topic>Cricetulus</topic><topic>Deoxyribonucleases, Type II Site-Specific</topic><topic>DHFR origin</topic><topic>DNA Helicases - metabolism</topic><topic>DNA Replication - drug effects</topic><topic>DNA-Binding Proteins - immunology</topic><topic>DNA-Binding Proteins - metabolism</topic><topic>DNA-Binding Proteins - pharmacology</topic><topic>DNA-Directed DNA Polymerase - metabolism</topic><topic>Haplorhini</topic><topic>HeLa Cells</topic><topic>Host Cell Factor C1</topic><topic>Humans</topic><topic>Ku antigen</topic><topic>Ku Autoantigen</topic><topic>Mammalian DNA replication</topic><topic>Nuclear Proteins - immunology</topic><topic>Nuclear Proteins - metabolism</topic><topic>Nuclear Proteins - pharmacology</topic><topic>Octamer Transcription Factor-1</topic><topic>Oligonucleotides - antagonists &amp; inhibitors</topic><topic>Oligonucleotides - pharmacology</topic><topic>Origin of DNA replication</topic><topic>Replication Origin</topic><topic>Replication Protein A</topic><topic>SV40 in vitro replication</topic><topic>Transcription Factors - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Matheos, Diamanto</creatorcontrib><creatorcontrib>Ruiz, Marcia T</creatorcontrib><creatorcontrib>Price, Gerald B</creatorcontrib><creatorcontrib>Zannis-Hadjopoulos, Maria</creatorcontrib><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>Biochimica et biophysica acta</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Matheos, Diamanto</au><au>Ruiz, Marcia T</au><au>Price, Gerald B</au><au>Zannis-Hadjopoulos, Maria</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ku antigen, an origin-specific binding protein that associates with replication proteins, is required for mammalian DNA replication</atitle><jtitle>Biochimica et biophysica acta</jtitle><addtitle>Biochim Biophys Acta</addtitle><date>2002-10-11</date><risdate>2002</risdate><volume>1578</volume><issue>1</issue><spage>59</spage><epage>72</epage><pages>59-72</pages><issn>0167-4781</issn><issn>0006-3002</issn><eissn>1879-2634</eissn><abstract>Ors binding activity (OBA) represents a HeLa cell protein activity that binds in a sequence-specific manner to A3/4, a 36-bp mammalian replication origin sequence. OBA's DNA binding domain is identical to the 80-kDa subunit of Ku antigen. Ku antigen associates with mammalian origins of DNA replication in vivo, with maximum binding at the G1/S phase. Addition of an A3/4 double-stranded oligonucleotide inhibited in vitro DNA replication of p186, p ors12, and pX24, plasmids containing the monkey replication origins of ors8, ors12, and the Chinese hamster DHFR oriβ, respectively. In contrast, in vitro SV40 DNA replication remained unaffected. The inhibitory effect of A3/4 oligonucleotide was fully reversed upon addition of affinity-purified Ku. Furthermore, depletion of Ku by inclusion of an antibody recognizing the Ku heterodimer, Ku70/Ku80, decreased mammalian replication to basal levels. By co-immunoprecipitation analyses, Ku was found to interact with DNA polymerases α, δ and ε, PCNA, topoisomerase II, RF-C, RP-A, DNA-PKcs, ORC-2, and Oct-1. These interactions were not inhibited by the presence of ethidium bromide in the immunoprecipitation reaction, suggesting DNA-independent protein associations. The data suggest an involvement of Ku in mammalian DNA replication as an origin-specific-binding protein with DNA helicase activity. Ku acts at the initiation step of replication and requires an A3/4-homologous sequence for origin binding. The physical association of Ku with replication proteins reveals a possible mechanism by which Ku is recruited to mammalian origins.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>12393188</pmid><doi>10.1016/S0167-4781(02)00497-9</doi><tpages>14</tpages></addata></record>
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source MEDLINE; Alma/SFX Local Collection
subjects Animals
Antibodies - pharmacology
Antigens, Nuclear
Cricetinae
Cricetulus
Deoxyribonucleases, Type II Site-Specific
DHFR origin
DNA Helicases - metabolism
DNA Replication - drug effects
DNA-Binding Proteins - immunology
DNA-Binding Proteins - metabolism
DNA-Binding Proteins - pharmacology
DNA-Directed DNA Polymerase - metabolism
Haplorhini
HeLa Cells
Host Cell Factor C1
Humans
Ku antigen
Ku Autoantigen
Mammalian DNA replication
Nuclear Proteins - immunology
Nuclear Proteins - metabolism
Nuclear Proteins - pharmacology
Octamer Transcription Factor-1
Oligonucleotides - antagonists & inhibitors
Oligonucleotides - pharmacology
Origin of DNA replication
Replication Origin
Replication Protein A
SV40 in vitro replication
Transcription Factors - metabolism
title Ku antigen, an origin-specific binding protein that associates with replication proteins, is required for mammalian DNA replication
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