Human replication protein Cdc6 prevents mitosis through a checkpoint mechanism that implicates Chk1
In yeasts, the replication protein Cdc6/Cdc18 is required for the initiation of DNA replication and also for coupling S phase with the following mitosis. In metazoans a role for Cdc6 has only been shown in S phase entry. Here we provide evidence that human Cdc6 (HuCdc6) also regulates the onset of m...
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creator | Clay-Farrace, Lorena Pelizon, Cristina Santamaria, David Pines, Jonathon Laskey, Ronald A. |
description | In yeasts, the replication protein Cdc6/Cdc18 is required for the initiation of DNA replication and also for coupling S phase with the following mitosis. In metazoans a role for Cdc6 has only been shown in S phase entry. Here we provide evidence that human Cdc6 (HuCdc6) also regulates the onset of mitosis, as overexpression of HuCdc6 in G
2
phase cells prevents entry into mitosis. This block is abolished when HuCdc6 is expressed together with a constitutively active Cyclin B/CDK1 complex or with Cdc25B or Cdc25C. An inhibitor of Chk1 kinase activity, UCN‐01, overcomes the HuCdc6 mediated G
2
arrest indicating that HuCdc6 blocks cells in G
2
phase via a checkpoint pathway involving Chk1. When HuCdc6 is overexpressed in G
2
, we detected phosphorylation of Chk1. Thus, HuCdc6 can trigger a checkpoint response, which could ensure that all DNA is replicated before mitotic entry. We also present evidence that the ability of HuCdc6 to block mitosis may be regulated by its phosphorylation. |
doi_str_mv | 10.1093/emboj/cdg046 |
format | Article |
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2
phase cells prevents entry into mitosis. This block is abolished when HuCdc6 is expressed together with a constitutively active Cyclin B/CDK1 complex or with Cdc25B or Cdc25C. An inhibitor of Chk1 kinase activity, UCN‐01, overcomes the HuCdc6 mediated G
2
arrest indicating that HuCdc6 blocks cells in G
2
phase via a checkpoint pathway involving Chk1. When HuCdc6 is overexpressed in G
2
, we detected phosphorylation of Chk1. Thus, HuCdc6 can trigger a checkpoint response, which could ensure that all DNA is replicated before mitotic entry. We also present evidence that the ability of HuCdc6 to block mitosis may be regulated by its phosphorylation.</description><identifier>ISSN: 0261-4189</identifier><identifier>ISSN: 1460-2075</identifier><identifier>EISSN: 1460-2075</identifier><identifier>DOI: 10.1093/emboj/cdg046</identifier><identifier>PMID: 12554670</identifier><identifier>CODEN: EMJODG</identifier><language>eng</language><publisher>Chichester, UK: John Wiley & Sons, Ltd</publisher><subject>Alkaloids - metabolism ; Cdc6 ; cell cycle ; Cell Cycle Proteins - genetics ; Cell Cycle Proteins - metabolism ; Checkpoint Kinase 1 ; checkpoint pathway ; Deoxyribonucleic acid ; DNA ; DNA Damage ; DNA Replication - physiology ; EMBO06 ; EMBO13 ; Enzyme Inhibitors - metabolism ; G2 phase ; HeLa Cells ; HuCdc6 ; Humans ; Microinjections ; Mitosis - physiology ; Mutation ; Nuclear Proteins - genetics ; Nuclear Proteins - metabolism ; Protein Kinases - metabolism ; Recombinant Fusion Proteins - genetics ; Recombinant Fusion Proteins - metabolism ; Staurosporine - analogs & derivatives ; Yeasts</subject><ispartof>The EMBO journal, 2003-02, Vol.22 (3), p.704-712</ispartof><rights>European Molecular Biology Organization 2003</rights><rights>Copyright © 2003 European Molecular Biology Organization</rights><rights>Copyright Oxford University Press(England) Feb 03, 2003</rights><rights>Copyright © 2003 European Molecular Biology Organization 2003</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5597-15908c28f299a8e290e25e619d82be1a24d6a2beb1d09e2da51f05f5d85885cd3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC140731/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC140731/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,1411,1427,27901,27902,45550,45551,46384,46808,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12554670$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Clay-Farrace, Lorena</creatorcontrib><creatorcontrib>Pelizon, Cristina</creatorcontrib><creatorcontrib>Santamaria, David</creatorcontrib><creatorcontrib>Pines, Jonathon</creatorcontrib><creatorcontrib>Laskey, Ronald A.</creatorcontrib><title>Human replication protein Cdc6 prevents mitosis through a checkpoint mechanism that implicates Chk1</title><title>The EMBO journal</title><addtitle>EMBO J</addtitle><addtitle>EMBO J</addtitle><description>In yeasts, the replication protein Cdc6/Cdc18 is required for the initiation of DNA replication and also for coupling S phase with the following mitosis. In metazoans a role for Cdc6 has only been shown in S phase entry. Here we provide evidence that human Cdc6 (HuCdc6) also regulates the onset of mitosis, as overexpression of HuCdc6 in G
2
phase cells prevents entry into mitosis. This block is abolished when HuCdc6 is expressed together with a constitutively active Cyclin B/CDK1 complex or with Cdc25B or Cdc25C. An inhibitor of Chk1 kinase activity, UCN‐01, overcomes the HuCdc6 mediated G
2
arrest indicating that HuCdc6 blocks cells in G
2
phase via a checkpoint pathway involving Chk1. When HuCdc6 is overexpressed in G
2
, we detected phosphorylation of Chk1. Thus, HuCdc6 can trigger a checkpoint response, which could ensure that all DNA is replicated before mitotic entry. We also present evidence that the ability of HuCdc6 to block mitosis may be regulated by its phosphorylation.</description><subject>Alkaloids - metabolism</subject><subject>Cdc6</subject><subject>cell cycle</subject><subject>Cell Cycle Proteins - genetics</subject><subject>Cell Cycle Proteins - metabolism</subject><subject>Checkpoint Kinase 1</subject><subject>checkpoint pathway</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA Damage</subject><subject>DNA Replication - physiology</subject><subject>EMBO06</subject><subject>EMBO13</subject><subject>Enzyme Inhibitors - metabolism</subject><subject>G2 phase</subject><subject>HeLa Cells</subject><subject>HuCdc6</subject><subject>Humans</subject><subject>Microinjections</subject><subject>Mitosis - physiology</subject><subject>Mutation</subject><subject>Nuclear Proteins - genetics</subject><subject>Nuclear Proteins - metabolism</subject><subject>Protein Kinases - metabolism</subject><subject>Recombinant Fusion Proteins - genetics</subject><subject>Recombinant Fusion Proteins - metabolism</subject><subject>Staurosporine - analogs & derivatives</subject><subject>Yeasts</subject><issn>0261-4189</issn><issn>1460-2075</issn><issn>1460-2075</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqFkUtv1DAUhSMEokNhxxpZLFgRajvxa8GijcoUVMqCIpaWx7kz8UwSBzvp499jyKgUhGBlW_c7x8c-Wfac4DcEq-IIupXfHtl6g0v-IFuQkuOcYsEeZgtMOclLItVB9iTGLcaYSUEeZweEMlZygReZPZs606MAQ-usGZ3v0RD8CK5HVW15OsAV9GNEnRt9dBGNTfDTpkEG2QbsbvCuH1EHtjG9i10amxG5bnaDiKpmR55mj9amjfBsvx5mX96dXlZn-fmn5fvq-Dy3jCmRE6awtFSuqVJGAlUYKANOVC3pCoihZc1N2q1IjRXQ2jCyxmzNasmkZLYuDrO3s-8wrTqobcodTKuH4DoTbrU3Tv8-6V2jN_5KkxKLgiT9q70--G8TxFF3LlpoW9ODn6IWVAlFivK_IJG8LAoqE_jyD3Drp9CnT9BEMcpTISpBr2fIBh9jgPVdYoL1j4r1z4r1XHHCX9x_5S9432kC2AxcuxZu_2mmTz-efBBMlYqJpMtnXUySfgPhXti_B9nzLo5wc3ePCTvNRSGY_nqx1J-r5cnygl5qWXwHhqjVFg</recordid><startdate>20030203</startdate><enddate>20030203</enddate><creator>Clay-Farrace, Lorena</creator><creator>Pelizon, Cristina</creator><creator>Santamaria, David</creator><creator>Pines, Jonathon</creator><creator>Laskey, Ronald A.</creator><general>John Wiley & Sons, Ltd</general><general>Nature Publishing Group UK</general><general>Springer Nature B.V</general><general>Oxford University Press</general><scope>BSCLL</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>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QP</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>BKSAR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M7N</scope><scope>M7P</scope><scope>MBDVC</scope><scope>P64</scope><scope>PCBAR</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20030203</creationdate><title>Human replication protein Cdc6 prevents mitosis through a checkpoint mechanism that implicates Chk1</title><author>Clay-Farrace, Lorena ; Pelizon, Cristina ; Santamaria, David ; Pines, Jonathon ; Laskey, Ronald A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5597-15908c28f299a8e290e25e619d82be1a24d6a2beb1d09e2da51f05f5d85885cd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Alkaloids - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The EMBO journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Clay-Farrace, Lorena</au><au>Pelizon, Cristina</au><au>Santamaria, David</au><au>Pines, Jonathon</au><au>Laskey, Ronald A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Human replication protein Cdc6 prevents mitosis through a checkpoint mechanism that implicates Chk1</atitle><jtitle>The EMBO journal</jtitle><stitle>EMBO J</stitle><addtitle>EMBO J</addtitle><date>2003-02-03</date><risdate>2003</risdate><volume>22</volume><issue>3</issue><spage>704</spage><epage>712</epage><pages>704-712</pages><issn>0261-4189</issn><issn>1460-2075</issn><eissn>1460-2075</eissn><coden>EMJODG</coden><abstract>In yeasts, the replication protein Cdc6/Cdc18 is required for the initiation of DNA replication and also for coupling S phase with the following mitosis. In metazoans a role for Cdc6 has only been shown in S phase entry. Here we provide evidence that human Cdc6 (HuCdc6) also regulates the onset of mitosis, as overexpression of HuCdc6 in G
2
phase cells prevents entry into mitosis. This block is abolished when HuCdc6 is expressed together with a constitutively active Cyclin B/CDK1 complex or with Cdc25B or Cdc25C. An inhibitor of Chk1 kinase activity, UCN‐01, overcomes the HuCdc6 mediated G
2
arrest indicating that HuCdc6 blocks cells in G
2
phase via a checkpoint pathway involving Chk1. When HuCdc6 is overexpressed in G
2
, we detected phosphorylation of Chk1. Thus, HuCdc6 can trigger a checkpoint response, which could ensure that all DNA is replicated before mitotic entry. We also present evidence that the ability of HuCdc6 to block mitosis may be regulated by its phosphorylation.</abstract><cop>Chichester, UK</cop><pub>John Wiley & Sons, Ltd</pub><pmid>12554670</pmid><doi>10.1093/emboj/cdg046</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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source | Wiley Free Content; MEDLINE; Wiley Online Library Journals Frontfile Complete; EZB-FREE-00999 freely available EZB journals; PubMed Central; Free Full-Text Journals in Chemistry |
subjects | Alkaloids - metabolism Cdc6 cell cycle Cell Cycle Proteins - genetics Cell Cycle Proteins - metabolism Checkpoint Kinase 1 checkpoint pathway Deoxyribonucleic acid DNA DNA Damage DNA Replication - physiology EMBO06 EMBO13 Enzyme Inhibitors - metabolism G2 phase HeLa Cells HuCdc6 Humans Microinjections Mitosis - physiology Mutation Nuclear Proteins - genetics Nuclear Proteins - metabolism Protein Kinases - metabolism Recombinant Fusion Proteins - genetics Recombinant Fusion Proteins - metabolism Staurosporine - analogs & derivatives Yeasts |
title | Human replication protein Cdc6 prevents mitosis through a checkpoint mechanism that implicates Chk1 |
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