Mammalian cyclin-dependent kinases
Cyclin-dependent kinases (Cdks) are the catalytic subunits of a family of mammalian heterodimeric serine/threonine kinases that have been implicated in the control of cell-cycle progression, transcription and neuronal function. Recent genetic evidence obtained with gene-targeted mice has shown that...
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Veröffentlicht in: | Trends in biochemical sciences (Amsterdam. Regular ed.) 2005-11, Vol.30 (11), p.630-641 |
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creator | Malumbres, Marcos Barbacid, Mariano |
description | Cyclin-dependent kinases (Cdks) are the catalytic subunits of a family of mammalian heterodimeric serine/threonine kinases that have been implicated in the control of cell-cycle progression, transcription and neuronal function. Recent genetic evidence obtained with gene-targeted mice has shown that Cdk4 and Cdk6 are not needed for entry into the cell cycle after mitogenic stimuli and organogenesis; however, they are essential for the proliferation of some endocrine and hematopoietic cells. Cdk2 is also dispensable for the mitotic cell cycle. Indeed, mice without Cdk2 are normal except for their complete sterility: unexpectedly, Cdk2 is crucial for the first meiotic division of male and female germ cells. These findings have important implications both for our current understanding of the role of Cdks in regulating the mammalian cell cycle and for their potential use as therapeutic targets in cancer. |
doi_str_mv | 10.1016/j.tibs.2005.09.005 |
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Recent genetic evidence obtained with gene-targeted mice has shown that Cdk4 and Cdk6 are not needed for entry into the cell cycle after mitogenic stimuli and organogenesis; however, they are essential for the proliferation of some endocrine and hematopoietic cells. Cdk2 is also dispensable for the mitotic cell cycle. Indeed, mice without Cdk2 are normal except for their complete sterility: unexpectedly, Cdk2 is crucial for the first meiotic division of male and female germ cells. 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These findings have important implications both for our current understanding of the role of Cdks in regulating the mammalian cell cycle and for their potential use as therapeutic targets in cancer.</description><subject>Animals</subject><subject>Cell Cycle - genetics</subject><subject>Cell Cycle - physiology</subject><subject>Cyclin-Dependent Kinase 2 - physiology</subject><subject>Cyclin-Dependent Kinases - genetics</subject><subject>Cyclin-Dependent Kinases - metabolism</subject><subject>Cyclin-Dependent Kinases - physiology</subject><subject>Humans</subject><subject>Mice</subject><subject>Models, Animal</subject><subject>Models, Biological</subject><subject>Neoplasms - drug therapy</subject><subject>Phylogeny</subject><subject>Transcription, Genetic</subject><issn>0968-0004</issn><issn>1362-4326</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kMtKA0EQRRtRTIz-gAsJLtzNWP2eATcSfEHEja6bnp4a6DiP2D0R8vfpkIA7V7cKTl2oQ8g1hZwCVferfPRVzBmAzKHMU5yQKeWKZYIzdUqmUKoiAwAxIRcxrgCo1FqekwlVjCtJyym5fbddZ1tv-7nbutb3WY1r7Gvsx_m3723EeEnOGttGvDrmjHw9P30uXrPlx8vb4nGZOS7FmHFZa9ZgAUWjFApbyQpZKbgVyjmqeRp0aR3XEtOCzCLoBhx1KCtrUfAZuTv0rsPws8E4ms5Hh21rexw20ahCS9BcJ5AdQBeGGAM2Zh18Z8PWUDB7M2Zl9mbM3oyB0qRIRzfH9k3VYf13clSRgIcDgOnHX4_BROexd1j7gG409eD_698BBMZz5Q</recordid><startdate>20051101</startdate><enddate>20051101</enddate><creator>Malumbres, Marcos</creator><creator>Barbacid, Mariano</creator><general>Elsevier Ltd</general><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>7X8</scope></search><sort><creationdate>20051101</creationdate><title>Mammalian cyclin-dependent kinases</title><author>Malumbres, Marcos ; Barbacid, Mariano</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c354t-35d72fe808f66e4ab5be2943a46cc1733a479ac375e733e2ae07f0c1ce5baae43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Animals</topic><topic>Cell Cycle - genetics</topic><topic>Cell Cycle - physiology</topic><topic>Cyclin-Dependent Kinase 2 - physiology</topic><topic>Cyclin-Dependent Kinases - genetics</topic><topic>Cyclin-Dependent Kinases - metabolism</topic><topic>Cyclin-Dependent Kinases - physiology</topic><topic>Humans</topic><topic>Mice</topic><topic>Models, Animal</topic><topic>Models, Biological</topic><topic>Neoplasms - drug therapy</topic><topic>Phylogeny</topic><topic>Transcription, Genetic</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Malumbres, Marcos</creatorcontrib><creatorcontrib>Barbacid, Mariano</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Trends in biochemical sciences (Amsterdam. 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subjects | Animals Cell Cycle - genetics Cell Cycle - physiology Cyclin-Dependent Kinase 2 - physiology Cyclin-Dependent Kinases - genetics Cyclin-Dependent Kinases - metabolism Cyclin-Dependent Kinases - physiology Humans Mice Models, Animal Models, Biological Neoplasms - drug therapy Phylogeny Transcription, Genetic |
title | Mammalian cyclin-dependent kinases |
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