CUL-4 ubiquitin ligase maintains genome stability by restraining DNA-replication licensing
To maintain genome stability, DNA replication is strictly regulated to occur only once per cell cycle. In eukaryotes, the presence of ‘licensing proteins’ at replication origins during the G1 cell-cycle phase allows the formation of the pre-replicative complex 1 . The removal of licensing proteins f...
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description | To maintain genome stability, DNA replication is strictly regulated to occur only once per cell cycle. In eukaryotes, the presence of ‘licensing proteins’ at replication origins during the G1 cell-cycle phase allows the formation of the pre-replicative complex
1
. The removal of licensing proteins from chromatin during the S phase ensures that origins fire only once per cell cycle
1
. Here we show that the CUL-4 ubiquitin ligase temporally restricts DNA-replication licensing in
Caenorhabditis elegans
. Inactivation of CUL-4 causes massive DNA re-replication, producing cells with up to 100C DNA content. The
C. elegans
orthologue of the replication-licensing factor Cdt1 (refs
2
,
3
) is required for DNA replication.
C. elegans
CDT-1 is present in G1-phase nuclei but disappears as cells enter S phase. In cells lacking CUL-4, CDT-1 levels fail to decrease during S phase and instead remain constant in the re-replicating cells. Removal of one genomic copy of
cdt-1
suppresses the
cul-4
re-replication phenotype. We propose that CUL-4 prevents aberrant re-initiation of DNA replication, at least in part, by facilitating the degradation of CDT-1. |
doi_str_mv | 10.1038/nature01747 |
format | Article |
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1
. The removal of licensing proteins from chromatin during the S phase ensures that origins fire only once per cell cycle
1
. Here we show that the CUL-4 ubiquitin ligase temporally restricts DNA-replication licensing in
Caenorhabditis elegans
. Inactivation of CUL-4 causes massive DNA re-replication, producing cells with up to 100C DNA content. The
C. elegans
orthologue of the replication-licensing factor Cdt1 (refs
2
,
3
) is required for DNA replication.
C. elegans
CDT-1 is present in G1-phase nuclei but disappears as cells enter S phase. In cells lacking CUL-4, CDT-1 levels fail to decrease during S phase and instead remain constant in the re-replicating cells. Removal of one genomic copy of
cdt-1
suppresses the
cul-4
re-replication phenotype. We propose that CUL-4 prevents aberrant re-initiation of DNA replication, at least in part, by facilitating the degradation of CDT-1.</description><identifier>ISSN: 0028-0836</identifier><identifier>EISSN: 1476-4687</identifier><identifier>DOI: 10.1038/nature01747</identifier><identifier>PMID: 12815436</identifier><identifier>CODEN: NATUAS</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>Animals ; Biological and medical sciences ; Caenorhabditis elegans - enzymology ; Caenorhabditis elegans - genetics ; Caenorhabditis elegans - metabolism ; Caenorhabditis elegans Proteins - genetics ; Caenorhabditis elegans Proteins - metabolism ; Cell Cycle ; Deoxyribonucleic acid ; DNA ; DNA Replication ; DNA, Helminth - analysis ; DNA, Helminth - biosynthesis ; DNA, Helminth - genetics ; Enzymes ; Fundamental and applied biological sciences. Psychology ; Genome ; Genomics ; Humanities and Social Sciences ; Inactivation ; letter ; Licensing ; Ligases - genetics ; Ligases - metabolism ; Molecular and cellular biology ; multidisciplinary ; RNA Interference ; RNA, Helminth - genetics ; RNA, Helminth - metabolism ; RNA, Messenger - genetics ; RNA, Messenger - metabolism ; Science ; Ubiquitin-Protein Ligases</subject><ispartof>Nature (London), 2003-06, Vol.423 (6942), p.885-889</ispartof><rights>Macmillan Magazines Ltd. 2003</rights><rights>2003 INIST-CNRS</rights><rights>COPYRIGHT 2003 Nature Publishing Group</rights><rights>Copyright Macmillan Journals Ltd. Jun 19, 2003</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c580t-8585752a66585f57fb950c236929cd016c821c78a3956f9e07ddb61e0d270a53</citedby><cites>FETCH-LOGICAL-c580t-8585752a66585f57fb950c236929cd016c821c78a3956f9e07ddb61e0d270a53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1038/nature01747$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/nature01747$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=14912513$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12815436$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhong, Weiwei</creatorcontrib><creatorcontrib>Feng, Hui</creatorcontrib><creatorcontrib>Santiago, Fernando E.</creatorcontrib><creatorcontrib>Kipreos, Edward T.</creatorcontrib><title>CUL-4 ubiquitin ligase maintains genome stability by restraining DNA-replication licensing</title><title>Nature (London)</title><addtitle>Nature</addtitle><addtitle>Nature</addtitle><description>To maintain genome stability, DNA replication is strictly regulated to occur only once per cell cycle. In eukaryotes, the presence of ‘licensing proteins’ at replication origins during the G1 cell-cycle phase allows the formation of the pre-replicative complex
1
. The removal of licensing proteins from chromatin during the S phase ensures that origins fire only once per cell cycle
1
. Here we show that the CUL-4 ubiquitin ligase temporally restricts DNA-replication licensing in
Caenorhabditis elegans
. Inactivation of CUL-4 causes massive DNA re-replication, producing cells with up to 100C DNA content. The
C. elegans
orthologue of the replication-licensing factor Cdt1 (refs
2
,
3
) is required for DNA replication.
C. elegans
CDT-1 is present in G1-phase nuclei but disappears as cells enter S phase. In cells lacking CUL-4, CDT-1 levels fail to decrease during S phase and instead remain constant in the re-replicating cells. Removal of one genomic copy of
cdt-1
suppresses the
cul-4
re-replication phenotype. We propose that CUL-4 prevents aberrant re-initiation of DNA replication, at least in part, by facilitating the degradation of CDT-1.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Caenorhabditis elegans - enzymology</subject><subject>Caenorhabditis elegans - genetics</subject><subject>Caenorhabditis elegans - metabolism</subject><subject>Caenorhabditis elegans Proteins - genetics</subject><subject>Caenorhabditis elegans Proteins - metabolism</subject><subject>Cell Cycle</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA Replication</subject><subject>DNA, Helminth - analysis</subject><subject>DNA, Helminth - biosynthesis</subject><subject>DNA, Helminth - genetics</subject><subject>Enzymes</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Genome</subject><subject>Genomics</subject><subject>Humanities and Social Sciences</subject><subject>Inactivation</subject><subject>letter</subject><subject>Licensing</subject><subject>Ligases - genetics</subject><subject>Ligases - metabolism</subject><subject>Molecular and cellular biology</subject><subject>multidisciplinary</subject><subject>RNA Interference</subject><subject>RNA, Helminth - genetics</subject><subject>RNA, Helminth - metabolism</subject><subject>RNA, Messenger - genetics</subject><subject>RNA, Messenger - metabolism</subject><subject>Science</subject><subject>Ubiquitin-Protein Ligases</subject><issn>0028-0836</issn><issn>1476-4687</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>BEC</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqF0l2L1DAUBuAgiruuXnkvRVhFtGu-k14O49fCoKDrjTclTdOSpU1nkhScf-9ZZmB2ZFBKacl5cpq-HISeE3xFMNPvg8lzdJgorh6gc8KVLLnU6iE6x5jqEmsmz9CTlG4xxgLUY3RGqCaCM3mOfi1_rkpezI3fzD77UAy-N8kVo_Ehw52K3oVpdEXKpvGDz9ui2RbRpRyh6kNffPi6KKNbD96a7Ke7BtaFBJWn6FFnhuSe7Z8X6ObTx5vll3L17fP1crEqrdA4l1pooQQ1UsJLJ1TXVAJbymRFK9tiIq2mxCptWCVkVzms2raRxOGWKmwEu0Cvd23XcdrMcLB69Mm6YTDBTXOqFWeEcqEVyFf_lowTziCv_0GiFeSnOcCXf8HbaY4B_rammAtGGSaAyh3qzeBqH7oJsrMQq4tmmILrPCwvoKcilRTy0PTI27Xf1PfR1QkEV-tGb092fXO0AUx2v3Nv5pTq6x_fj-3bnbVxSim6rl5HP5q4rQmu72auvjdzoF_sQ5ib0bUHux8yAJd7YJI1QxdNsD4dHK8IFYSBe7dzCUqhd_GQ5qnv_gHYruoL</recordid><startdate>20030619</startdate><enddate>20030619</enddate><creator>Zhong, Weiwei</creator><creator>Feng, Hui</creator><creator>Santiago, Fernando E.</creator><creator>Kipreos, Edward T.</creator><general>Nature Publishing Group UK</general><general>Nature Publishing</general><general>Nature Publishing Group</general><scope>IQODW</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>7QR</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7ST</scope><scope>7T5</scope><scope>7TG</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88G</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BEC</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>BKSAR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</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>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>M2O</scope><scope>M2P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PCBAR</scope><scope>PDBOC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PSYQQ</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>Q9U</scope><scope>R05</scope><scope>RC3</scope><scope>S0X</scope><scope>SOI</scope><scope>7X8</scope><scope>7SC</scope><scope>7SP</scope><scope>7SR</scope><scope>7TB</scope><scope>7U5</scope><scope>8BQ</scope><scope>F28</scope><scope>JG9</scope><scope>JQ2</scope><scope>KR7</scope><scope>L7M</scope><scope>L~C</scope><scope>L~D</scope></search><sort><creationdate>20030619</creationdate><title>CUL-4 ubiquitin ligase maintains genome stability by restraining DNA-replication licensing</title><author>Zhong, Weiwei ; Feng, Hui ; Santiago, Fernando E. ; Kipreos, Edward T.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c580t-8585752a66585f57fb950c236929cd016c821c78a3956f9e07ddb61e0d270a53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Caenorhabditis elegans - enzymology</topic><topic>Caenorhabditis elegans - genetics</topic><topic>Caenorhabditis elegans - metabolism</topic><topic>Caenorhabditis elegans Proteins - genetics</topic><topic>Caenorhabditis elegans Proteins - metabolism</topic><topic>Cell Cycle</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>DNA Replication</topic><topic>DNA, Helminth - analysis</topic><topic>DNA, Helminth - biosynthesis</topic><topic>DNA, Helminth - genetics</topic><topic>Enzymes</topic><topic>Fundamental and applied biological sciences. 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In eukaryotes, the presence of ‘licensing proteins’ at replication origins during the G1 cell-cycle phase allows the formation of the pre-replicative complex
1
. The removal of licensing proteins from chromatin during the S phase ensures that origins fire only once per cell cycle
1
. Here we show that the CUL-4 ubiquitin ligase temporally restricts DNA-replication licensing in
Caenorhabditis elegans
. Inactivation of CUL-4 causes massive DNA re-replication, producing cells with up to 100C DNA content. The
C. elegans
orthologue of the replication-licensing factor Cdt1 (refs
2
,
3
) is required for DNA replication.
C. elegans
CDT-1 is present in G1-phase nuclei but disappears as cells enter S phase. In cells lacking CUL-4, CDT-1 levels fail to decrease during S phase and instead remain constant in the re-replicating cells. Removal of one genomic copy of
cdt-1
suppresses the
cul-4
re-replication phenotype. We propose that CUL-4 prevents aberrant re-initiation of DNA replication, at least in part, by facilitating the degradation of CDT-1.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>12815436</pmid><doi>10.1038/nature01747</doi><tpages>5</tpages></addata></record> |
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subjects | Animals Biological and medical sciences Caenorhabditis elegans - enzymology Caenorhabditis elegans - genetics Caenorhabditis elegans - metabolism Caenorhabditis elegans Proteins - genetics Caenorhabditis elegans Proteins - metabolism Cell Cycle Deoxyribonucleic acid DNA DNA Replication DNA, Helminth - analysis DNA, Helminth - biosynthesis DNA, Helminth - genetics Enzymes Fundamental and applied biological sciences. Psychology Genome Genomics Humanities and Social Sciences Inactivation letter Licensing Ligases - genetics Ligases - metabolism Molecular and cellular biology multidisciplinary RNA Interference RNA, Helminth - genetics RNA, Helminth - metabolism RNA, Messenger - genetics RNA, Messenger - metabolism Science Ubiquitin-Protein Ligases |
title | CUL-4 ubiquitin ligase maintains genome stability by restraining DNA-replication licensing |
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