Microtubule minus-end anchorage at centrosomal and non-centrosomal sites: the role of ninein
The novel concept of a centrosomal anchoring complex, which is distinct from the gamma-tubulin nucleating complex, has previously been proposed following studies on cochlear epithelial cells. In this investigation we present evidence from two different cell systems which suggests that the centrosoma...
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Veröffentlicht in: | Journal of cell science 2000-09, Vol.113 ( Pt 17) (17), p.3013-3023 |
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creator | Mogensen, M M Malik, A Piel, M Bouckson-Castaing, V Bornens, M |
description | The novel concept of a centrosomal anchoring complex, which is distinct from the gamma-tubulin nucleating complex, has previously been proposed following studies on cochlear epithelial cells. In this investigation we present evidence from two different cell systems which suggests that the centrosomal protein ninein is a strong candidate for the proposed anchoring complex. Ninein has recently been observed in cultured fibroblast cells to localise primarily to the post-mitotic mother centriole, which is the focus for a classic radial microtubule array. We show here by immunoelectron microscopical analyses of centrosomes from mouse L929 cells that ninein concentrates at the appendages surrounding the mother centriole and at the microtubule minus-ends. We further show that localisation of ninein in the cochlear supporting epithelial cells, where the vast majority of the microtubule minus-ends are associated with apical non-centrosomal sites, suggests that it is not directly involved in microtubule nucleation. Ninein seems to play an important role in the positioning and anchorage of the microtubule minus-ends in these epithelial cells. Evidence is presented which suggests that ninein is released from the centrosome, translocated with the microtubules, and is responsible for the anchorage of microtubule minus-ends to the apical sites. We propose that ninein is a non-nucleating microtubule minus-end associated protein which may have a dual role as a minus-end capping and anchoring protein. |
doi_str_mv | 10.1242/jcs.113.17.3013 |
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In this investigation we present evidence from two different cell systems which suggests that the centrosomal protein ninein is a strong candidate for the proposed anchoring complex. Ninein has recently been observed in cultured fibroblast cells to localise primarily to the post-mitotic mother centriole, which is the focus for a classic radial microtubule array. We show here by immunoelectron microscopical analyses of centrosomes from mouse L929 cells that ninein concentrates at the appendages surrounding the mother centriole and at the microtubule minus-ends. We further show that localisation of ninein in the cochlear supporting epithelial cells, where the vast majority of the microtubule minus-ends are associated with apical non-centrosomal sites, suggests that it is not directly involved in microtubule nucleation. Ninein seems to play an important role in the positioning and anchorage of the microtubule minus-ends in these epithelial cells. Evidence is presented which suggests that ninein is released from the centrosome, translocated with the microtubules, and is responsible for the anchorage of microtubule minus-ends to the apical sites. 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In this investigation we present evidence from two different cell systems which suggests that the centrosomal protein ninein is a strong candidate for the proposed anchoring complex. Ninein has recently been observed in cultured fibroblast cells to localise primarily to the post-mitotic mother centriole, which is the focus for a classic radial microtubule array. We show here by immunoelectron microscopical analyses of centrosomes from mouse L929 cells that ninein concentrates at the appendages surrounding the mother centriole and at the microtubule minus-ends. We further show that localisation of ninein in the cochlear supporting epithelial cells, where the vast majority of the microtubule minus-ends are associated with apical non-centrosomal sites, suggests that it is not directly involved in microtubule nucleation. Ninein seems to play an important role in the positioning and anchorage of the microtubule minus-ends in these epithelial cells. Evidence is presented which suggests that ninein is released from the centrosome, translocated with the microtubules, and is responsible for the anchorage of microtubule minus-ends to the apical sites. We propose that ninein is a non-nucleating microtubule minus-end associated protein which may have a dual role as a minus-end capping and anchoring protein.</description><subject>Animals</subject><subject>Calcium-Binding Proteins - analysis</subject><subject>Calcium-Binding Proteins - genetics</subject><subject>Cell Line</subject><subject>Centrosome - metabolism</subject><subject>Centrosome - ultrastructure</subject><subject>centrosomes</subject><subject>Chromosomal Proteins, Non-Histone</subject><subject>Cytoskeletal Proteins</subject><subject>Green Fluorescent Proteins</subject><subject>GTP-Binding Proteins - drug effects</subject><subject>GTP-Binding Proteins - metabolism</subject><subject>GTP-Binding Proteins - physiology</subject><subject>In Vitro Techniques</subject><subject>Indicators and Reagents - pharmacology</subject><subject>Luminescent Proteins - genetics</subject><subject>Luminescent Proteins - pharmacology</subject><subject>Mice</subject><subject>Microscopy, Fluorescence</subject><subject>Microscopy, Immunoelectron</subject><subject>Microtubules - drug effects</subject><subject>Microtubules - metabolism</subject><subject>Microtubules - ultrastructure</subject><subject>Models, Biological</subject><subject>ninein</subject><subject>Nocodazole - pharmacology</subject><subject>Nuclear Proteins</subject><subject>Organ of Corti - cytology</subject><subject>Organ of Corti - metabolism</subject><subject>Recombinant Fusion Proteins - metabolism</subject><issn>0021-9533</issn><issn>1477-9137</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkD1PwzAQQC0EoqUws6FMbEl9dpyL2VDFl1TEAhuS5TgOTZXYxU4G_j2p2oGN6aS7d294hFwDzYDlbLk1MQPgGWDGKfATMoccMZXA8ZTMKWWQSsH5jFzEuKWUIpN4TmZAJc9pTufk87U1wQ9jNXY26Vs3xtS6OtHObHzQXzbRQ2KsG4KPvtfddKgT5136dxfbwca7ZNjYJPhJ45vEtc627pKcNbqL9uo4F-Tj8eF99Zyu355eVvfr1OQMh9RKgXllCl7RWpaFpJRL2ZQ1qysEgFIU2gjUtqrLujJMiKIwGoXgsgTN85wvyO3Buwv-e7RxUH0bje067awfo0LAghcC_wWhBIYM6QQuD-AUJ8ZgG7ULba_DjwKq9uXVVF5N5RWg2pefPm6O6rHqbf2HP6Tmv1TOfyU</recordid><startdate>20000901</startdate><enddate>20000901</enddate><creator>Mogensen, M M</creator><creator>Malik, A</creator><creator>Piel, M</creator><creator>Bouckson-Castaing, V</creator><creator>Bornens, M</creator><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>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20000901</creationdate><title>Microtubule minus-end anchorage at centrosomal and non-centrosomal sites: the role of ninein</title><author>Mogensen, M M ; Malik, A ; Piel, M ; Bouckson-Castaing, V ; Bornens, M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c427t-e9574bc63b0d986900399f8d2db7111856ac57aebd8dbc25566ca7553981a3443</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Animals</topic><topic>Calcium-Binding Proteins - analysis</topic><topic>Calcium-Binding Proteins - genetics</topic><topic>Cell Line</topic><topic>Centrosome - metabolism</topic><topic>Centrosome - ultrastructure</topic><topic>centrosomes</topic><topic>Chromosomal Proteins, Non-Histone</topic><topic>Cytoskeletal Proteins</topic><topic>Green Fluorescent Proteins</topic><topic>GTP-Binding Proteins - drug effects</topic><topic>GTP-Binding Proteins - metabolism</topic><topic>GTP-Binding Proteins - physiology</topic><topic>In Vitro Techniques</topic><topic>Indicators and Reagents - pharmacology</topic><topic>Luminescent Proteins - genetics</topic><topic>Luminescent Proteins - pharmacology</topic><topic>Mice</topic><topic>Microscopy, Fluorescence</topic><topic>Microscopy, Immunoelectron</topic><topic>Microtubules - drug effects</topic><topic>Microtubules - metabolism</topic><topic>Microtubules - ultrastructure</topic><topic>Models, Biological</topic><topic>ninein</topic><topic>Nocodazole - pharmacology</topic><topic>Nuclear Proteins</topic><topic>Organ of Corti - cytology</topic><topic>Organ of Corti - metabolism</topic><topic>Recombinant Fusion Proteins - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mogensen, M M</creatorcontrib><creatorcontrib>Malik, A</creatorcontrib><creatorcontrib>Piel, M</creatorcontrib><creatorcontrib>Bouckson-Castaing, V</creatorcontrib><creatorcontrib>Bornens, M</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of cell science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mogensen, M M</au><au>Malik, A</au><au>Piel, M</au><au>Bouckson-Castaing, V</au><au>Bornens, M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Microtubule minus-end anchorage at centrosomal and non-centrosomal sites: the role of ninein</atitle><jtitle>Journal of cell science</jtitle><addtitle>J Cell Sci</addtitle><date>2000-09-01</date><risdate>2000</risdate><volume>113 ( Pt 17)</volume><issue>17</issue><spage>3013</spage><epage>3023</epage><pages>3013-3023</pages><issn>0021-9533</issn><eissn>1477-9137</eissn><abstract>The novel concept of a centrosomal anchoring complex, which is distinct from the gamma-tubulin nucleating complex, has previously been proposed following studies on cochlear epithelial cells. In this investigation we present evidence from two different cell systems which suggests that the centrosomal protein ninein is a strong candidate for the proposed anchoring complex. Ninein has recently been observed in cultured fibroblast cells to localise primarily to the post-mitotic mother centriole, which is the focus for a classic radial microtubule array. We show here by immunoelectron microscopical analyses of centrosomes from mouse L929 cells that ninein concentrates at the appendages surrounding the mother centriole and at the microtubule minus-ends. We further show that localisation of ninein in the cochlear supporting epithelial cells, where the vast majority of the microtubule minus-ends are associated with apical non-centrosomal sites, suggests that it is not directly involved in microtubule nucleation. Ninein seems to play an important role in the positioning and anchorage of the microtubule minus-ends in these epithelial cells. 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subjects | Animals Calcium-Binding Proteins - analysis Calcium-Binding Proteins - genetics Cell Line Centrosome - metabolism Centrosome - ultrastructure centrosomes Chromosomal Proteins, Non-Histone Cytoskeletal Proteins Green Fluorescent Proteins GTP-Binding Proteins - drug effects GTP-Binding Proteins - metabolism GTP-Binding Proteins - physiology In Vitro Techniques Indicators and Reagents - pharmacology Luminescent Proteins - genetics Luminescent Proteins - pharmacology Mice Microscopy, Fluorescence Microscopy, Immunoelectron Microtubules - drug effects Microtubules - metabolism Microtubules - ultrastructure Models, Biological ninein Nocodazole - pharmacology Nuclear Proteins Organ of Corti - cytology Organ of Corti - metabolism Recombinant Fusion Proteins - metabolism |
title | Microtubule minus-end anchorage at centrosomal and non-centrosomal sites: the role of ninein |
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