SP600125 suppresses Cdk1 and induces endoreplication directly from G2 phase, independent of JNK inhibition
Cell cycle controls ensure that DNA replication (S phase) follows mitosis resulting in two precise copies of the genome. A failure of the control mechanisms can result in multiple rounds of DNA replication without cell division. In endoreplication, cells with replicated genomes bypass mitosis, then...
Gespeichert in:
Veröffentlicht in: | Oncogene 2010-03, Vol.29 (11), p.1702-1716 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 1716 |
---|---|
container_issue | 11 |
container_start_page | 1702 |
container_title | Oncogene |
container_volume | 29 |
creator | Kim, J A Lee, J Margolis, R L Fotedar, R |
description | Cell cycle controls ensure that DNA replication (S phase) follows mitosis resulting in two precise copies of the genome. A failure of the control mechanisms can result in multiple rounds of DNA replication without cell division. In endoreplication, cells with replicated genomes bypass mitosis, then replicate their DNA again, resulting in polyploidy. Endoreplication from G2 phase lacks all hallmarks of mitosis. Using synchronized cells, we show that the c-Jun N-terminal kinase (JNK) inhibitor, SP600125, prevents the entry of cells into mitosis and leads to endoreplication of DNA from G2 phase. We show that cells proceed from G2 phase to replicate their DNA in the absence of mitosis. This effect of SP600125 is independent of its suppression of JNK activity. Instead, the inhibitory effect of SP600125 on mitotic entry predominantly occurs upstream of Aurora A kinase and Polo-like kinase 1, resulting in a failure to remove the inhibitory phosphorylation of Cdk1. Importantly, our results directly show that the inhibition of Cdk1 activity and the persistence of Cdk2 activity in G2 cells induces endoreplication without mitosis. Furthermore, endoreplication from G2 phase is independent of p53 control. |
doi_str_mv | 10.1038/onc.2009.464 |
format | Article |
fullrecord | <record><control><sourceid>gale_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3145494</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A222252638</galeid><sourcerecordid>A222252638</sourcerecordid><originalsourceid>FETCH-LOGICAL-c605t-a634b9df37890fe82212bd3e27dea1d3eb770f22d990afbf33c996c6a1ddfc193</originalsourceid><addsrcrecordid>eNp1kttrFDEUhwdR7Fp981kGRXzprLln8iKUReulqKA-h0wuu1lnk2kyI_S_N8OuXSs1eUg45ztXflX1FIIlBLh9HYNeIgDEkjByr1pAwllDqSD3qwUQFDQCYXRSPcp5CwDgAqCH1UnhGQKcL6rtt68MAIhonadhSDZnm-uV-QlrFUztg5l0MdhgYrJD77UafQy18cnqsb-uXYq7-gLVw0ZlezbzdiiwDWMdXf3x86di2vjOz1GPqwdO9dk-Obyn1Y93b7-v3jeXXy4-rM4vG80AHRvFMOmEcZi3AjjbIgRRZ7BF3FgFy6fjHDiEjBBAuc5hrIVgmhWfcRoKfFq92ecdpm5njS7NJNXLIfmdStcyKi9ve4LfyHX8JTEklAhSErw6JEjxarJ5lDufte17FWycsuSEMEhZywv54h9yG6cUynQSMQJxQQQu1PP_UohjxgGlx1Rr1Vvpg4ulNz0XlueoHIoYbgu1vIMq19id1zFY54v9VsDZPkCnmHOy7mYPEMhZP7LoR876kUU_BX_29-5u4D-CKcDLA6CyVr1LKmifjxziFLVwrtvsuVxcYW3TceY7C_8GhGLagg</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>227367055</pqid></control><display><type>article</type><title>SP600125 suppresses Cdk1 and induces endoreplication directly from G2 phase, independent of JNK inhibition</title><source>MEDLINE</source><source>Springer Nature - Complete Springer Journals</source><source>Nature Journals Online</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><creator>Kim, J A ; Lee, J ; Margolis, R L ; Fotedar, R</creator><creatorcontrib>Kim, J A ; Lee, J ; Margolis, R L ; Fotedar, R</creatorcontrib><description>Cell cycle controls ensure that DNA replication (S phase) follows mitosis resulting in two precise copies of the genome. A failure of the control mechanisms can result in multiple rounds of DNA replication without cell division. In endoreplication, cells with replicated genomes bypass mitosis, then replicate their DNA again, resulting in polyploidy. Endoreplication from G2 phase lacks all hallmarks of mitosis. Using synchronized cells, we show that the c-Jun N-terminal kinase (JNK) inhibitor, SP600125, prevents the entry of cells into mitosis and leads to endoreplication of DNA from G2 phase. We show that cells proceed from G2 phase to replicate their DNA in the absence of mitosis. This effect of SP600125 is independent of its suppression of JNK activity. Instead, the inhibitory effect of SP600125 on mitotic entry predominantly occurs upstream of Aurora A kinase and Polo-like kinase 1, resulting in a failure to remove the inhibitory phosphorylation of Cdk1. Importantly, our results directly show that the inhibition of Cdk1 activity and the persistence of Cdk2 activity in G2 cells induces endoreplication without mitosis. Furthermore, endoreplication from G2 phase is independent of p53 control.</description><identifier>ISSN: 0950-9232</identifier><identifier>EISSN: 1476-5594</identifier><identifier>DOI: 10.1038/onc.2009.464</identifier><identifier>PMID: 20062077</identifier><identifier>CODEN: ONCNES</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/92/436/2388 ; Anthracenes - pharmacology ; Apoptosis ; Aurora Kinases ; Biological and medical sciences ; Blotting, Western ; c-Jun protein ; CDC2 Protein Kinase - antagonists & inhibitors ; CDC2 Protein Kinase - metabolism ; Cell Biology ; Cell cycle ; Cell Cycle Proteins - metabolism ; Cell division ; Cell Line, Tumor ; Cell physiology ; Cell transformation and carcinogenesis. Action of oncogenes and antioncogenes ; Cyclin B - metabolism ; Cyclin-Dependent Kinase 2 - metabolism ; Deoxyribonucleic acid ; DNA ; DNA biosynthesis ; DNA replication ; DNA Replication - drug effects ; Enzyme Activation - drug effects ; Enzyme inhibitors ; Flow Cytometry ; Fundamental and applied biological sciences. Psychology ; G2 phase ; G2 Phase - drug effects ; G2 Phase - genetics ; G2 Phase - physiology ; Genetic aspects ; Genomes ; Genomics ; HCT116 Cells ; Health aspects ; Human Genetics ; Humans ; Internal Medicine ; JNK Mitogen-Activated Protein Kinases - antagonists & inhibitors ; JNK Mitogen-Activated Protein Kinases - genetics ; JNK Mitogen-Activated Protein Kinases - metabolism ; JNK protein ; Medicine ; Medicine & Public Health ; Mitosis ; Mitosis - drug effects ; Molecular and cellular biology ; Oncology ; original-article ; Phosphorylation ; Phosphorylation - drug effects ; Physiological aspects ; Polo-like kinase ; Polo-Like Kinase 1 ; Polyploidy ; Protein Serine-Threonine Kinases - metabolism ; Proto-Oncogene Proteins - metabolism ; Replication ; RNA Interference ; S phase ; Transcription factors ; Tumor suppressor genes ; Tumor Suppressor Protein p53 - metabolism</subject><ispartof>Oncogene, 2010-03, Vol.29 (11), p.1702-1716</ispartof><rights>Macmillan Publishers Limited 2010</rights><rights>2015 INIST-CNRS</rights><rights>COPYRIGHT 2010 Nature Publishing Group</rights><rights>Copyright Nature Publishing Group Mar 18, 2010</rights><rights>Macmillan Publishers Limited 2010.</rights><rights>2010 Macmillan Publishers Limited All rights reserved 2010</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c605t-a634b9df37890fe82212bd3e27dea1d3eb770f22d990afbf33c996c6a1ddfc193</citedby><cites>FETCH-LOGICAL-c605t-a634b9df37890fe82212bd3e27dea1d3eb770f22d990afbf33c996c6a1ddfc193</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/onc.2009.464$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/onc.2009.464$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>230,314,776,780,881,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=22752818$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20062077$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kim, J A</creatorcontrib><creatorcontrib>Lee, J</creatorcontrib><creatorcontrib>Margolis, R L</creatorcontrib><creatorcontrib>Fotedar, R</creatorcontrib><title>SP600125 suppresses Cdk1 and induces endoreplication directly from G2 phase, independent of JNK inhibition</title><title>Oncogene</title><addtitle>Oncogene</addtitle><addtitle>Oncogene</addtitle><description>Cell cycle controls ensure that DNA replication (S phase) follows mitosis resulting in two precise copies of the genome. A failure of the control mechanisms can result in multiple rounds of DNA replication without cell division. In endoreplication, cells with replicated genomes bypass mitosis, then replicate their DNA again, resulting in polyploidy. Endoreplication from G2 phase lacks all hallmarks of mitosis. Using synchronized cells, we show that the c-Jun N-terminal kinase (JNK) inhibitor, SP600125, prevents the entry of cells into mitosis and leads to endoreplication of DNA from G2 phase. We show that cells proceed from G2 phase to replicate their DNA in the absence of mitosis. This effect of SP600125 is independent of its suppression of JNK activity. Instead, the inhibitory effect of SP600125 on mitotic entry predominantly occurs upstream of Aurora A kinase and Polo-like kinase 1, resulting in a failure to remove the inhibitory phosphorylation of Cdk1. Importantly, our results directly show that the inhibition of Cdk1 activity and the persistence of Cdk2 activity in G2 cells induces endoreplication without mitosis. Furthermore, endoreplication from G2 phase is independent of p53 control.</description><subject>631/92/436/2388</subject><subject>Anthracenes - pharmacology</subject><subject>Apoptosis</subject><subject>Aurora Kinases</subject><subject>Biological and medical sciences</subject><subject>Blotting, Western</subject><subject>c-Jun protein</subject><subject>CDC2 Protein Kinase - antagonists & inhibitors</subject><subject>CDC2 Protein Kinase - metabolism</subject><subject>Cell Biology</subject><subject>Cell cycle</subject><subject>Cell Cycle Proteins - metabolism</subject><subject>Cell division</subject><subject>Cell Line, Tumor</subject><subject>Cell physiology</subject><subject>Cell transformation and carcinogenesis. Action of oncogenes and antioncogenes</subject><subject>Cyclin B - metabolism</subject><subject>Cyclin-Dependent Kinase 2 - metabolism</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA biosynthesis</subject><subject>DNA replication</subject><subject>DNA Replication - drug effects</subject><subject>Enzyme Activation - drug effects</subject><subject>Enzyme inhibitors</subject><subject>Flow Cytometry</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>G2 phase</subject><subject>G2 Phase - drug effects</subject><subject>G2 Phase - genetics</subject><subject>G2 Phase - physiology</subject><subject>Genetic aspects</subject><subject>Genomes</subject><subject>Genomics</subject><subject>HCT116 Cells</subject><subject>Health aspects</subject><subject>Human Genetics</subject><subject>Humans</subject><subject>Internal Medicine</subject><subject>JNK Mitogen-Activated Protein Kinases - antagonists & inhibitors</subject><subject>JNK Mitogen-Activated Protein Kinases - genetics</subject><subject>JNK Mitogen-Activated Protein Kinases - metabolism</subject><subject>JNK protein</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Mitosis</subject><subject>Mitosis - drug effects</subject><subject>Molecular and cellular biology</subject><subject>Oncology</subject><subject>original-article</subject><subject>Phosphorylation</subject><subject>Phosphorylation - drug effects</subject><subject>Physiological aspects</subject><subject>Polo-like kinase</subject><subject>Polo-Like Kinase 1</subject><subject>Polyploidy</subject><subject>Protein Serine-Threonine Kinases - metabolism</subject><subject>Proto-Oncogene Proteins - metabolism</subject><subject>Replication</subject><subject>RNA Interference</subject><subject>S phase</subject><subject>Transcription factors</subject><subject>Tumor suppressor genes</subject><subject>Tumor Suppressor Protein p53 - metabolism</subject><issn>0950-9232</issn><issn>1476-5594</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNp1kttrFDEUhwdR7Fp981kGRXzprLln8iKUReulqKA-h0wuu1lnk2kyI_S_N8OuXSs1eUg45ztXflX1FIIlBLh9HYNeIgDEkjByr1pAwllDqSD3qwUQFDQCYXRSPcp5CwDgAqCH1UnhGQKcL6rtt68MAIhonadhSDZnm-uV-QlrFUztg5l0MdhgYrJD77UafQy18cnqsb-uXYq7-gLVw0ZlezbzdiiwDWMdXf3x86di2vjOz1GPqwdO9dk-Obyn1Y93b7-v3jeXXy4-rM4vG80AHRvFMOmEcZi3AjjbIgRRZ7BF3FgFy6fjHDiEjBBAuc5hrIVgmhWfcRoKfFq92ecdpm5njS7NJNXLIfmdStcyKi9ve4LfyHX8JTEklAhSErw6JEjxarJ5lDufte17FWycsuSEMEhZywv54h9yG6cUynQSMQJxQQQu1PP_UohjxgGlx1Rr1Vvpg4ulNz0XlueoHIoYbgu1vIMq19id1zFY54v9VsDZPkCnmHOy7mYPEMhZP7LoR876kUU_BX_29-5u4D-CKcDLA6CyVr1LKmifjxziFLVwrtvsuVxcYW3TceY7C_8GhGLagg</recordid><startdate>20100318</startdate><enddate>20100318</enddate><creator>Kim, J A</creator><creator>Lee, J</creator><creator>Margolis, R L</creator><creator>Fotedar, R</creator><general>Nature Publishing Group UK</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>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>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</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>M7P</scope><scope>MBDVC</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>RC3</scope><scope>5PM</scope></search><sort><creationdate>20100318</creationdate><title>SP600125 suppresses Cdk1 and induces endoreplication directly from G2 phase, independent of JNK inhibition</title><author>Kim, J A ; Lee, J ; Margolis, R L ; Fotedar, R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c605t-a634b9df37890fe82212bd3e27dea1d3eb770f22d990afbf33c996c6a1ddfc193</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>631/92/436/2388</topic><topic>Anthracenes - pharmacology</topic><topic>Apoptosis</topic><topic>Aurora Kinases</topic><topic>Biological and medical sciences</topic><topic>Blotting, Western</topic><topic>c-Jun protein</topic><topic>CDC2 Protein Kinase - antagonists & inhibitors</topic><topic>CDC2 Protein Kinase - metabolism</topic><topic>Cell Biology</topic><topic>Cell cycle</topic><topic>Cell Cycle Proteins - metabolism</topic><topic>Cell division</topic><topic>Cell Line, Tumor</topic><topic>Cell physiology</topic><topic>Cell transformation and carcinogenesis. Action of oncogenes and antioncogenes</topic><topic>Cyclin B - metabolism</topic><topic>Cyclin-Dependent Kinase 2 - metabolism</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>DNA biosynthesis</topic><topic>DNA replication</topic><topic>DNA Replication - drug effects</topic><topic>Enzyme Activation - drug effects</topic><topic>Enzyme inhibitors</topic><topic>Flow Cytometry</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>G2 phase</topic><topic>G2 Phase - drug effects</topic><topic>G2 Phase - genetics</topic><topic>G2 Phase - physiology</topic><topic>Genetic aspects</topic><topic>Genomes</topic><topic>Genomics</topic><topic>HCT116 Cells</topic><topic>Health aspects</topic><topic>Human Genetics</topic><topic>Humans</topic><topic>Internal Medicine</topic><topic>JNK Mitogen-Activated Protein Kinases - antagonists & inhibitors</topic><topic>JNK Mitogen-Activated Protein Kinases - genetics</topic><topic>JNK Mitogen-Activated Protein Kinases - metabolism</topic><topic>JNK protein</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Mitosis</topic><topic>Mitosis - drug effects</topic><topic>Molecular and cellular biology</topic><topic>Oncology</topic><topic>original-article</topic><topic>Phosphorylation</topic><topic>Phosphorylation - drug effects</topic><topic>Physiological aspects</topic><topic>Polo-like kinase</topic><topic>Polo-Like Kinase 1</topic><topic>Polyploidy</topic><topic>Protein Serine-Threonine Kinases - metabolism</topic><topic>Proto-Oncogene Proteins - metabolism</topic><topic>Replication</topic><topic>RNA Interference</topic><topic>S phase</topic><topic>Transcription factors</topic><topic>Tumor suppressor genes</topic><topic>Tumor Suppressor Protein p53 - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kim, J A</creatorcontrib><creatorcontrib>Lee, J</creatorcontrib><creatorcontrib>Margolis, R L</creatorcontrib><creatorcontrib>Fotedar, R</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>Genetics Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Oncogene</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kim, J A</au><au>Lee, J</au><au>Margolis, R L</au><au>Fotedar, R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>SP600125 suppresses Cdk1 and induces endoreplication directly from G2 phase, independent of JNK inhibition</atitle><jtitle>Oncogene</jtitle><stitle>Oncogene</stitle><addtitle>Oncogene</addtitle><date>2010-03-18</date><risdate>2010</risdate><volume>29</volume><issue>11</issue><spage>1702</spage><epage>1716</epage><pages>1702-1716</pages><issn>0950-9232</issn><eissn>1476-5594</eissn><coden>ONCNES</coden><abstract>Cell cycle controls ensure that DNA replication (S phase) follows mitosis resulting in two precise copies of the genome. A failure of the control mechanisms can result in multiple rounds of DNA replication without cell division. In endoreplication, cells with replicated genomes bypass mitosis, then replicate their DNA again, resulting in polyploidy. Endoreplication from G2 phase lacks all hallmarks of mitosis. Using synchronized cells, we show that the c-Jun N-terminal kinase (JNK) inhibitor, SP600125, prevents the entry of cells into mitosis and leads to endoreplication of DNA from G2 phase. We show that cells proceed from G2 phase to replicate their DNA in the absence of mitosis. This effect of SP600125 is independent of its suppression of JNK activity. Instead, the inhibitory effect of SP600125 on mitotic entry predominantly occurs upstream of Aurora A kinase and Polo-like kinase 1, resulting in a failure to remove the inhibitory phosphorylation of Cdk1. Importantly, our results directly show that the inhibition of Cdk1 activity and the persistence of Cdk2 activity in G2 cells induces endoreplication without mitosis. Furthermore, endoreplication from G2 phase is independent of p53 control.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>20062077</pmid><doi>10.1038/onc.2009.464</doi><tpages>15</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0950-9232 |
ispartof | Oncogene, 2010-03, Vol.29 (11), p.1702-1716 |
issn | 0950-9232 1476-5594 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3145494 |
source | MEDLINE; Springer Nature - Complete Springer Journals; Nature Journals Online; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals |
subjects | 631/92/436/2388 Anthracenes - pharmacology Apoptosis Aurora Kinases Biological and medical sciences Blotting, Western c-Jun protein CDC2 Protein Kinase - antagonists & inhibitors CDC2 Protein Kinase - metabolism Cell Biology Cell cycle Cell Cycle Proteins - metabolism Cell division Cell Line, Tumor Cell physiology Cell transformation and carcinogenesis. Action of oncogenes and antioncogenes Cyclin B - metabolism Cyclin-Dependent Kinase 2 - metabolism Deoxyribonucleic acid DNA DNA biosynthesis DNA replication DNA Replication - drug effects Enzyme Activation - drug effects Enzyme inhibitors Flow Cytometry Fundamental and applied biological sciences. Psychology G2 phase G2 Phase - drug effects G2 Phase - genetics G2 Phase - physiology Genetic aspects Genomes Genomics HCT116 Cells Health aspects Human Genetics Humans Internal Medicine JNK Mitogen-Activated Protein Kinases - antagonists & inhibitors JNK Mitogen-Activated Protein Kinases - genetics JNK Mitogen-Activated Protein Kinases - metabolism JNK protein Medicine Medicine & Public Health Mitosis Mitosis - drug effects Molecular and cellular biology Oncology original-article Phosphorylation Phosphorylation - drug effects Physiological aspects Polo-like kinase Polo-Like Kinase 1 Polyploidy Protein Serine-Threonine Kinases - metabolism Proto-Oncogene Proteins - metabolism Replication RNA Interference S phase Transcription factors Tumor suppressor genes Tumor Suppressor Protein p53 - metabolism |
title | SP600125 suppresses Cdk1 and induces endoreplication directly from G2 phase, independent of JNK inhibition |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-09T23%3A55%3A06IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=SP600125%20suppresses%20Cdk1%20and%20induces%20endoreplication%20directly%20from%20G2%20phase,%20independent%20of%20JNK%20inhibition&rft.jtitle=Oncogene&rft.au=Kim,%20J%20A&rft.date=2010-03-18&rft.volume=29&rft.issue=11&rft.spage=1702&rft.epage=1716&rft.pages=1702-1716&rft.issn=0950-9232&rft.eissn=1476-5594&rft.coden=ONCNES&rft_id=info:doi/10.1038/onc.2009.464&rft_dat=%3Cgale_pubme%3EA222252638%3C/gale_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=227367055&rft_id=info:pmid/20062077&rft_galeid=A222252638&rfr_iscdi=true |