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...

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Veröffentlicht in:Oncogene 2010-03, Vol.29 (11), p.1702-1716
Hauptverfasser: Kim, J A, Lee, J, Margolis, R L, Fotedar, R
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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
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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 &amp; inhibitors ; JNK Mitogen-Activated Protein Kinases - genetics ; JNK Mitogen-Activated Protein Kinases - metabolism ; JNK protein ; Medicine ; Medicine &amp; 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&amp;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. 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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
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