Inhibition of S/G2 Phase CDK4 Reduces Mitotic Fidelity
Cyclin-dependent kinase 4 (CDK4)/cyclin D has a key role in regulating progression through late G1 into S phase of the cell cycle. CDK4-cyclin D complexes then persist through the latter phases of the cell cycle, although little is known about their potential roles. We have developed small molecule...
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Veröffentlicht in: | The Journal of biological chemistry 2006-04, Vol.281 (15), p.9987-9995 |
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creator | Burgess, Andrew Wigan, Matthew Giles, Nichole DePinto, Wanda Gillespie, Paul Stevens, Frankie Gabrielli, Brian |
description | Cyclin-dependent kinase 4 (CDK4)/cyclin D has a key role in regulating progression through late G1 into S phase of the cell cycle. CDK4-cyclin D complexes then persist through the latter phases of the cell cycle, although little is known about their potential roles. We have developed small molecule inhibitors that are highly selective for CDK4 and have used these to define a role for CDK4-cyclin D in G2 phase. The addition of the CDK4 inhibitor or small interfering RNA knockdown of cyclin D3, the cyclin D partner, delayed progression through G2 phase and mitosis. The G2 phase delay was independent of ATM/ATR and p38 MAPK but associated with elevated Wee1. The mitotic delay was because of failure of chromosomes to migrate to the metaphase plate. However, cells eventually exited mitosis, with a resultant increase in cells with multiple or micronuclei. Inhibiting CDK4 delayed the expression of the chromosomal passenger proteins survivin and borealin, although this was unlikely to account for the mitotic phenotype. These data provide evidence for a novel function for CDK4-cyclin D3 activity in S and G2 phase that is critical for G2/M progression and the fidelity of mitosis. |
doi_str_mv | 10.1074/jbc.M512714200 |
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CDK4-cyclin D complexes then persist through the latter phases of the cell cycle, although little is known about their potential roles. We have developed small molecule inhibitors that are highly selective for CDK4 and have used these to define a role for CDK4-cyclin D in G2 phase. The addition of the CDK4 inhibitor or small interfering RNA knockdown of cyclin D3, the cyclin D partner, delayed progression through G2 phase and mitosis. The G2 phase delay was independent of ATM/ATR and p38 MAPK but associated with elevated Wee1. The mitotic delay was because of failure of chromosomes to migrate to the metaphase plate. However, cells eventually exited mitosis, with a resultant increase in cells with multiple or micronuclei. Inhibiting CDK4 delayed the expression of the chromosomal passenger proteins survivin and borealin, although this was unlikely to account for the mitotic phenotype. These data provide evidence for a novel function for CDK4-cyclin D3 activity in S and G2 phase that is critical for G2/M progression and the fidelity of mitosis.</description><identifier>ISSN: 0021-9258</identifier><identifier>EISSN: 1083-351X</identifier><identifier>DOI: 10.1074/jbc.M512714200</identifier><identifier>PMID: 16476733</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Caffeine - pharmacology ; Cell Cycle ; Cell Cycle Proteins - metabolism ; Cell Line ; Cell Proliferation ; Cyclin-Dependent Kinase 4 - chemistry ; Cyclin-Dependent Kinase 4 - metabolism ; DNA, Complementary - metabolism ; Enzyme Inhibitors - pharmacology ; G1 Phase ; G2 Phase ; HeLa Cells ; Humans ; Imidazoles - pharmacology ; Inhibitor of Apoptosis Proteins ; Inhibitory Concentration 50 ; Kinetics ; Microtubule-Associated Proteins - metabolism ; Mitosis ; Models, Chemical ; Neoplasm Proteins - metabolism ; p38 Mitogen-Activated Protein Kinases - metabolism ; Phenotype ; Phosphorylation ; Protein Binding ; Proto-Oncogene Proteins c-akt - metabolism ; Pyridines - pharmacology ; Retinoblastoma Protein - metabolism ; Reverse Transcriptase Polymerase Chain Reaction ; RNA - chemistry ; RNA, Small Interfering - metabolism ; S Phase ; Survivin ; Time Factors</subject><ispartof>The Journal of biological chemistry, 2006-04, Vol.281 (15), p.9987-9995</ispartof><rights>2006 © 2006 ASBMB. Currently published by Elsevier Inc; originally published by American Society for Biochemistry and Molecular Biology.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3490-8c4ca113bb50c485aa2b84e75a0b20dfbbc7dc3d1a39db10a3a8218416c9a2283</citedby><cites>FETCH-LOGICAL-c3490-8c4ca113bb50c485aa2b84e75a0b20dfbbc7dc3d1a39db10a3a8218416c9a2283</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16476733$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Burgess, Andrew</creatorcontrib><creatorcontrib>Wigan, Matthew</creatorcontrib><creatorcontrib>Giles, Nichole</creatorcontrib><creatorcontrib>DePinto, Wanda</creatorcontrib><creatorcontrib>Gillespie, Paul</creatorcontrib><creatorcontrib>Stevens, Frankie</creatorcontrib><creatorcontrib>Gabrielli, Brian</creatorcontrib><title>Inhibition of S/G2 Phase CDK4 Reduces Mitotic Fidelity</title><title>The Journal of biological chemistry</title><addtitle>J Biol Chem</addtitle><description>Cyclin-dependent kinase 4 (CDK4)/cyclin D has a key role in regulating progression through late G1 into S phase of the cell cycle. 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These data provide evidence for a novel function for CDK4-cyclin D3 activity in S and G2 phase that is critical for G2/M progression and the fidelity of mitosis.</description><subject>Animals</subject><subject>Caffeine - pharmacology</subject><subject>Cell Cycle</subject><subject>Cell Cycle Proteins - metabolism</subject><subject>Cell Line</subject><subject>Cell Proliferation</subject><subject>Cyclin-Dependent Kinase 4 - chemistry</subject><subject>Cyclin-Dependent Kinase 4 - metabolism</subject><subject>DNA, Complementary - metabolism</subject><subject>Enzyme Inhibitors - pharmacology</subject><subject>G1 Phase</subject><subject>G2 Phase</subject><subject>HeLa Cells</subject><subject>Humans</subject><subject>Imidazoles - pharmacology</subject><subject>Inhibitor of Apoptosis Proteins</subject><subject>Inhibitory Concentration 50</subject><subject>Kinetics</subject><subject>Microtubule-Associated Proteins - metabolism</subject><subject>Mitosis</subject><subject>Models, Chemical</subject><subject>Neoplasm Proteins - metabolism</subject><subject>p38 Mitogen-Activated Protein Kinases - metabolism</subject><subject>Phenotype</subject><subject>Phosphorylation</subject><subject>Protein Binding</subject><subject>Proto-Oncogene Proteins c-akt - metabolism</subject><subject>Pyridines - pharmacology</subject><subject>Retinoblastoma Protein - metabolism</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>RNA - chemistry</subject><subject>RNA, Small Interfering - metabolism</subject><subject>S Phase</subject><subject>Survivin</subject><subject>Time Factors</subject><issn>0021-9258</issn><issn>1083-351X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kM1PwkAUxDdGI_hx9ahNPBff292226NBQSNGo5J42-xX6RKgpFs0_PeWlIST7zKX30zeDCFXCAOEjN_NtRm8Jkgz5BTgiPQRBItZgt_HpA9AMc5pInrkLIQ5tMdzPCU9THmWZoz1Sfq8Kr32ja9WUVVEn3djGr2XKrho-PDCow9nN8aF6NU3VeNNNPLWLXyzvSAnhVoEd7nXczIdPX4Nn-LJ2_h5eD-JDeM5xMJwoxCZ1gkYLhKlqBbcZYkCTcEWWpvMGmZRsdxqBMWUoCg4piZXlAp2TgZdrqmrEGpXyHXtl6reSgS5G0C2A8jDAK3hujOsN3rp7AHfN26B2w4o_az89bWT2lemdEtJBUpMZJ6LrKVuOqpQlVSz2gc5_aSADBDaGLojREe4tv6Pd7UMxruVcbbNNI20lf_vxz8SdHuu</recordid><startdate>20060414</startdate><enddate>20060414</enddate><creator>Burgess, Andrew</creator><creator>Wigan, Matthew</creator><creator>Giles, Nichole</creator><creator>DePinto, Wanda</creator><creator>Gillespie, Paul</creator><creator>Stevens, Frankie</creator><creator>Gabrielli, Brian</creator><general>Elsevier Inc</general><general>American Society for Biochemistry and Molecular Biology</general><scope>6I.</scope><scope>AAFTH</scope><scope>FBQ</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></search><sort><creationdate>20060414</creationdate><title>Inhibition of S/G2 Phase CDK4 Reduces Mitotic Fidelity</title><author>Burgess, Andrew ; Wigan, Matthew ; Giles, Nichole ; DePinto, Wanda ; Gillespie, Paul ; Stevens, Frankie ; Gabrielli, Brian</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3490-8c4ca113bb50c485aa2b84e75a0b20dfbbc7dc3d1a39db10a3a8218416c9a2283</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Animals</topic><topic>Caffeine - pharmacology</topic><topic>Cell Cycle</topic><topic>Cell Cycle Proteins - metabolism</topic><topic>Cell Line</topic><topic>Cell Proliferation</topic><topic>Cyclin-Dependent Kinase 4 - chemistry</topic><topic>Cyclin-Dependent Kinase 4 - metabolism</topic><topic>DNA, Complementary - metabolism</topic><topic>Enzyme Inhibitors - pharmacology</topic><topic>G1 Phase</topic><topic>G2 Phase</topic><topic>HeLa Cells</topic><topic>Humans</topic><topic>Imidazoles - pharmacology</topic><topic>Inhibitor of Apoptosis Proteins</topic><topic>Inhibitory Concentration 50</topic><topic>Kinetics</topic><topic>Microtubule-Associated Proteins - metabolism</topic><topic>Mitosis</topic><topic>Models, Chemical</topic><topic>Neoplasm Proteins - metabolism</topic><topic>p38 Mitogen-Activated Protein Kinases - metabolism</topic><topic>Phenotype</topic><topic>Phosphorylation</topic><topic>Protein Binding</topic><topic>Proto-Oncogene Proteins c-akt - metabolism</topic><topic>Pyridines - pharmacology</topic><topic>Retinoblastoma Protein - metabolism</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>RNA - chemistry</topic><topic>RNA, Small Interfering - metabolism</topic><topic>S Phase</topic><topic>Survivin</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Burgess, Andrew</creatorcontrib><creatorcontrib>Wigan, Matthew</creatorcontrib><creatorcontrib>Giles, Nichole</creatorcontrib><creatorcontrib>DePinto, Wanda</creatorcontrib><creatorcontrib>Gillespie, Paul</creatorcontrib><creatorcontrib>Stevens, Frankie</creatorcontrib><creatorcontrib>Gabrielli, Brian</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>The Journal of biological chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Burgess, Andrew</au><au>Wigan, Matthew</au><au>Giles, Nichole</au><au>DePinto, Wanda</au><au>Gillespie, Paul</au><au>Stevens, Frankie</au><au>Gabrielli, Brian</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Inhibition of S/G2 Phase CDK4 Reduces Mitotic Fidelity</atitle><jtitle>The Journal of biological chemistry</jtitle><addtitle>J Biol Chem</addtitle><date>2006-04-14</date><risdate>2006</risdate><volume>281</volume><issue>15</issue><spage>9987</spage><epage>9995</epage><pages>9987-9995</pages><issn>0021-9258</issn><eissn>1083-351X</eissn><abstract>Cyclin-dependent kinase 4 (CDK4)/cyclin D has a key role in regulating progression through late G1 into S phase of the cell cycle. CDK4-cyclin D complexes then persist through the latter phases of the cell cycle, although little is known about their potential roles. We have developed small molecule inhibitors that are highly selective for CDK4 and have used these to define a role for CDK4-cyclin D in G2 phase. The addition of the CDK4 inhibitor or small interfering RNA knockdown of cyclin D3, the cyclin D partner, delayed progression through G2 phase and mitosis. The G2 phase delay was independent of ATM/ATR and p38 MAPK but associated with elevated Wee1. The mitotic delay was because of failure of chromosomes to migrate to the metaphase plate. However, cells eventually exited mitosis, with a resultant increase in cells with multiple or micronuclei. Inhibiting CDK4 delayed the expression of the chromosomal passenger proteins survivin and borealin, although this was unlikely to account for the mitotic phenotype. 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subjects | Animals Caffeine - pharmacology Cell Cycle Cell Cycle Proteins - metabolism Cell Line Cell Proliferation Cyclin-Dependent Kinase 4 - chemistry Cyclin-Dependent Kinase 4 - metabolism DNA, Complementary - metabolism Enzyme Inhibitors - pharmacology G1 Phase G2 Phase HeLa Cells Humans Imidazoles - pharmacology Inhibitor of Apoptosis Proteins Inhibitory Concentration 50 Kinetics Microtubule-Associated Proteins - metabolism Mitosis Models, Chemical Neoplasm Proteins - metabolism p38 Mitogen-Activated Protein Kinases - metabolism Phenotype Phosphorylation Protein Binding Proto-Oncogene Proteins c-akt - metabolism Pyridines - pharmacology Retinoblastoma Protein - metabolism Reverse Transcriptase Polymerase Chain Reaction RNA - chemistry RNA, Small Interfering - metabolism S Phase Survivin Time Factors |
title | Inhibition of S/G2 Phase CDK4 Reduces Mitotic Fidelity |
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