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cdc2 links the Drosophila cell cycle and asymmetric division machineries
Asymmetric cell divisions can be mediated by the preferential segregation of cell-fate determinants into one of two sibling daughters. In Drosophila neural progenitors, Inscuteable, Partner of Inscuteable and Bazooka localize as an apical cortical complex at interphase, which directs the apical-basa...
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Published in: | Nature (London) 2001-02, Vol.409 (6823), p.1063-1067 |
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creator | Chia, William Tio, Murni Udolph, Gerald Yang, Xiaohang |
description | Asymmetric cell divisions can be mediated by the preferential segregation of cell-fate determinants into one of two sibling daughters. In Drosophila neural progenitors, Inscuteable, Partner of Inscuteable and Bazooka localize as an apical cortical complex at interphase, which directs the apical-basal orientation of the mitotic spindle as well as the basal/cortical localization of the cell-fate determinants Numb and/or Prospero during mitosis. Although localization of these proteins shows dependence on the cell cycle, the involvement of cell-cycle components in asymmetric divisions has not been demonstrated. Here we show that neural progenitor asymmetric divisions require the cell-cycle regulator cdc2. By attenuating Drosophila cdc2 function without blocking mitosis, normally asymmetric progenitor divisions become defective, failing to correctly localize asymmetric components during mitosis and/or to resolve distinct sibling fates. cdc2 is not necessary for initiating apical complex formation during interphase; however, maintaining the asymmetric localization of the apical components during mitosis requires Cdc2/B-type cyclin complexes. Our findings link cdc2 with asymmetric divisions, and explain why the asymmetric localization of molecules like Inscuteable show cell-cycle dependence. |
doi_str_mv | 10.1038/35059124 |
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In Drosophila neural progenitors, Inscuteable, Partner of Inscuteable and Bazooka localize as an apical cortical complex at interphase, which directs the apical-basal orientation of the mitotic spindle as well as the basal/cortical localization of the cell-fate determinants Numb and/or Prospero during mitosis. Although localization of these proteins shows dependence on the cell cycle, the involvement of cell-cycle components in asymmetric divisions has not been demonstrated. Here we show that neural progenitor asymmetric divisions require the cell-cycle regulator cdc2. By attenuating Drosophila cdc2 function without blocking mitosis, normally asymmetric progenitor divisions become defective, failing to correctly localize asymmetric components during mitosis and/or to resolve distinct sibling fates. cdc2 is not necessary for initiating apical complex formation during interphase; however, maintaining the asymmetric localization of the apical components during mitosis requires Cdc2/B-type cyclin complexes. Our findings link cdc2 with asymmetric divisions, and explain why the asymmetric localization of molecules like Inscuteable show cell-cycle dependence.</description><identifier>ISSN: 0028-0836</identifier><identifier>EISSN: 1476-4687</identifier><identifier>DOI: 10.1038/35059124</identifier><identifier>PMID: 11234018</identifier><identifier>CODEN: NATUAS</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>Animals ; Asymmetry ; Biological and medical sciences ; Carrier Proteins - physiology ; Cdc2 protein ; CDC2 Protein Kinase - genetics ; CDC2 Protein Kinase - physiology ; Cell Cycle ; Cell Cycle Proteins - physiology ; Cell Division ; Cells ; Central Nervous System - cytology ; Cyclins - metabolism ; Cytoskeletal Proteins - physiology ; Determinants ; Division ; Drosophila ; Drosophila Proteins ; Embryology: invertebrates and vertebrates. Teratology ; Embryos ; Fundamental and applied biological sciences. Psychology ; Genotype ; Humanities and Social Sciences ; Insects ; letter ; Links ; Localization ; Mitosis ; multidisciplinary ; Mutation ; Nerve Tissue Proteins - physiology ; Nervous system ; Neuropeptides ; Nuclear Proteins - physiology ; Organogenesis. Fetal development ; Organogenesis. Physiological fonctions ; Phenotype ; Phosphorylation ; Position (location) ; Proteins ; Science ; Science (multidisciplinary) ; Transcription Factors</subject><ispartof>Nature (London), 2001-02, Vol.409 (6823), p.1063-1067</ispartof><rights>Macmillan Magazines Ltd. 2001</rights><rights>2001 INIST-CNRS</rights><rights>COPYRIGHT 2001 Nature Publishing Group</rights><rights>Copyright Macmillan Journals Ltd. 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In Drosophila neural progenitors, Inscuteable, Partner of Inscuteable and Bazooka localize as an apical cortical complex at interphase, which directs the apical-basal orientation of the mitotic spindle as well as the basal/cortical localization of the cell-fate determinants Numb and/or Prospero during mitosis. Although localization of these proteins shows dependence on the cell cycle, the involvement of cell-cycle components in asymmetric divisions has not been demonstrated. Here we show that neural progenitor asymmetric divisions require the cell-cycle regulator cdc2. 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Our findings link cdc2 with asymmetric divisions, and explain why the asymmetric localization of molecules like Inscuteable show cell-cycle dependence.</description><subject>Animals</subject><subject>Asymmetry</subject><subject>Biological and medical sciences</subject><subject>Carrier Proteins - physiology</subject><subject>Cdc2 protein</subject><subject>CDC2 Protein Kinase - genetics</subject><subject>CDC2 Protein Kinase - physiology</subject><subject>Cell Cycle</subject><subject>Cell Cycle Proteins - physiology</subject><subject>Cell Division</subject><subject>Cells</subject><subject>Central Nervous System - cytology</subject><subject>Cyclins - metabolism</subject><subject>Cytoskeletal Proteins - physiology</subject><subject>Determinants</subject><subject>Division</subject><subject>Drosophila</subject><subject>Drosophila Proteins</subject><subject>Embryology: invertebrates and vertebrates. 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Academic</collection><jtitle>Nature (London)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chia, William</au><au>Tio, Murni</au><au>Udolph, Gerald</au><au>Yang, Xiaohang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>cdc2 links the Drosophila cell cycle and asymmetric division machineries</atitle><jtitle>Nature (London)</jtitle><stitle>Nature</stitle><addtitle>Nature</addtitle><date>2001-02-22</date><risdate>2001</risdate><volume>409</volume><issue>6823</issue><spage>1063</spage><epage>1067</epage><pages>1063-1067</pages><issn>0028-0836</issn><eissn>1476-4687</eissn><coden>NATUAS</coden><abstract>Asymmetric cell divisions can be mediated by the preferential segregation of cell-fate determinants into one of two sibling daughters. In Drosophila neural progenitors, Inscuteable, Partner of Inscuteable and Bazooka localize as an apical cortical complex at interphase, which directs the apical-basal orientation of the mitotic spindle as well as the basal/cortical localization of the cell-fate determinants Numb and/or Prospero during mitosis. Although localization of these proteins shows dependence on the cell cycle, the involvement of cell-cycle components in asymmetric divisions has not been demonstrated. Here we show that neural progenitor asymmetric divisions require the cell-cycle regulator cdc2. By attenuating Drosophila cdc2 function without blocking mitosis, normally asymmetric progenitor divisions become defective, failing to correctly localize asymmetric components during mitosis and/or to resolve distinct sibling fates. cdc2 is not necessary for initiating apical complex formation during interphase; however, maintaining the asymmetric localization of the apical components during mitosis requires Cdc2/B-type cyclin complexes. Our findings link cdc2 with asymmetric divisions, and explain why the asymmetric localization of molecules like Inscuteable show cell-cycle dependence.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>11234018</pmid><doi>10.1038/35059124</doi><tpages>5</tpages></addata></record> |
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subjects | Animals Asymmetry Biological and medical sciences Carrier Proteins - physiology Cdc2 protein CDC2 Protein Kinase - genetics CDC2 Protein Kinase - physiology Cell Cycle Cell Cycle Proteins - physiology Cell Division Cells Central Nervous System - cytology Cyclins - metabolism Cytoskeletal Proteins - physiology Determinants Division Drosophila Drosophila Proteins Embryology: invertebrates and vertebrates. Teratology Embryos Fundamental and applied biological sciences. Psychology Genotype Humanities and Social Sciences Insects letter Links Localization Mitosis multidisciplinary Mutation Nerve Tissue Proteins - physiology Nervous system Neuropeptides Nuclear Proteins - physiology Organogenesis. Fetal development Organogenesis. Physiological fonctions Phenotype Phosphorylation Position (location) Proteins Science Science (multidisciplinary) Transcription Factors |
title | cdc2 links the Drosophila cell cycle and asymmetric division machineries |
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