CP39, CP75 and CP91 are major structural components of the Dictyostelium centrosome’s core structure
The acentriolar Dictyostelium centrosome is a nucleus-associated body consisting of a core structure with three plaque-like layers, which are surrounded by a microtubule-nucleating corona. The core duplicates once per cell cycle at the G2/M transition, whereby its central layer disappears and the tw...
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Veröffentlicht in: | European journal of cell biology 2017-03, Vol.96 (2), p.119-130 |
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creator | Meyer, Irene Peter, Tatjana Batsios, Petros Kuhnert, Oliver Krüger-Genge, Anne Camurça, Carl Gräf, Ralph |
description | The acentriolar Dictyostelium centrosome is a nucleus-associated body consisting of a core structure with three plaque-like layers, which are surrounded by a microtubule-nucleating corona. The core duplicates once per cell cycle at the G2/M transition, whereby its central layer disappears and the two outer layers form the mitotic spindle poles. Through proteomic analysis of isolated centrosomes, we have identified CP39 and CP75, two essential components of the core structure. Both proteins can be assigned to the central core layer as their centrosomal presence is correlated to the disappearance and reappearance of the central core layer in the course of centrosome duplication. Both proteins contain domains with centrosome-binding activity in their N- and C-terminal halves, whereby the respective N-terminal half is required for cell cycle-dependent regulation. CP39 is capable of self-interaction and GFP-CP39 overexpression elicited supernumerary microtubule-organizing centers and pre-centrosomal cytosolic clusters. Underexpression stopped cell growth and reversed the MTOC amplification phenotype. In contrast, in case of CP75 underexpression of the protein by RNAi treatment elicited supernumerary MTOCs. In addition, CP75RNAi affects correct chromosome segregation and causes co-depletion of CP39 and CP91, another central core layer component. CP39 and CP75 interact with each other directly in a yeast two-hybrid assay. Furthermore, CP39, CP75 and CP91 mutually interact in a proximity-dependent biotin identification (BioID) assay. Our data indicate that these three proteins are all required for proper centrosome biogenesis and make up the major structural components of core structure's central layer. |
doi_str_mv | 10.1016/j.ejcb.2017.01.004 |
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The core duplicates once per cell cycle at the G2/M transition, whereby its central layer disappears and the two outer layers form the mitotic spindle poles. Through proteomic analysis of isolated centrosomes, we have identified CP39 and CP75, two essential components of the core structure. Both proteins can be assigned to the central core layer as their centrosomal presence is correlated to the disappearance and reappearance of the central core layer in the course of centrosome duplication. Both proteins contain domains with centrosome-binding activity in their N- and C-terminal halves, whereby the respective N-terminal half is required for cell cycle-dependent regulation. CP39 is capable of self-interaction and GFP-CP39 overexpression elicited supernumerary microtubule-organizing centers and pre-centrosomal cytosolic clusters. Underexpression stopped cell growth and reversed the MTOC amplification phenotype. In contrast, in case of CP75 underexpression of the protein by RNAi treatment elicited supernumerary MTOCs. In addition, CP75RNAi affects correct chromosome segregation and causes co-depletion of CP39 and CP91, another central core layer component. CP39 and CP75 interact with each other directly in a yeast two-hybrid assay. Furthermore, CP39, CP75 and CP91 mutually interact in a proximity-dependent biotin identification (BioID) assay. Our data indicate that these three proteins are all required for proper centrosome biogenesis and make up the major structural components of core structure's central layer.</description><identifier>ISSN: 0171-9335</identifier><identifier>EISSN: 1618-1298</identifier><identifier>DOI: 10.1016/j.ejcb.2017.01.004</identifier><identifier>PMID: 28104305</identifier><language>eng</language><publisher>Germany: Elsevier GmbH</publisher><subject>Animals ; Centrosome ; Centrosome - metabolism ; Dictyostelium ; Dictyostelium - cytology ; Dictyostelium - metabolism ; Microtubules ; Microtubules - metabolism ; Mitosis ; Mitosis - physiology ; Nucleus ; Protozoan Proteins - metabolism</subject><ispartof>European journal of cell biology, 2017-03, Vol.96 (2), p.119-130</ispartof><rights>2017 Elsevier GmbH</rights><rights>Copyright © 2017 Elsevier GmbH. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c271t-ab8073197fe0892eefbca0addce6515675b29d593b8e5e6a689f644c606c1cff3</citedby><cites>FETCH-LOGICAL-c271t-ab8073197fe0892eefbca0addce6515675b29d593b8e5e6a689f644c606c1cff3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.ejcb.2017.01.004$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,781,785,3551,27928,27929,45999</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28104305$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Meyer, Irene</creatorcontrib><creatorcontrib>Peter, Tatjana</creatorcontrib><creatorcontrib>Batsios, Petros</creatorcontrib><creatorcontrib>Kuhnert, Oliver</creatorcontrib><creatorcontrib>Krüger-Genge, Anne</creatorcontrib><creatorcontrib>Camurça, Carl</creatorcontrib><creatorcontrib>Gräf, Ralph</creatorcontrib><title>CP39, CP75 and CP91 are major structural components of the Dictyostelium centrosome’s core structure</title><title>European journal of cell biology</title><addtitle>Eur J Cell Biol</addtitle><description>The acentriolar Dictyostelium centrosome is a nucleus-associated body consisting of a core structure with three plaque-like layers, which are surrounded by a microtubule-nucleating corona. 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In contrast, in case of CP75 underexpression of the protein by RNAi treatment elicited supernumerary MTOCs. In addition, CP75RNAi affects correct chromosome segregation and causes co-depletion of CP39 and CP91, another central core layer component. CP39 and CP75 interact with each other directly in a yeast two-hybrid assay. Furthermore, CP39, CP75 and CP91 mutually interact in a proximity-dependent biotin identification (BioID) assay. Our data indicate that these three proteins are all required for proper centrosome biogenesis and make up the major structural components of core structure's central layer.</description><subject>Animals</subject><subject>Centrosome</subject><subject>Centrosome - metabolism</subject><subject>Dictyostelium</subject><subject>Dictyostelium - cytology</subject><subject>Dictyostelium - metabolism</subject><subject>Microtubules</subject><subject>Microtubules - metabolism</subject><subject>Mitosis</subject><subject>Mitosis - physiology</subject><subject>Nucleus</subject><subject>Protozoan Proteins - metabolism</subject><issn>0171-9335</issn><issn>1618-1298</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kMFO3DAQhq2qVdnSvgCHysceSOpJYseWuKAtpUhIcICz5ThjkSiJt7ZTiRuv0dfrk-DVAseextJ8_6_xR8gJsBIYiO9jiaPtyopBWzIoGWvekQ0IkAVUSr4nm7yAQtU1PyKfYhwZAy6V-kiOKgmsqRnfELe9rdUp3d62nJqlzw8F1ASksxl9oDGF1aY1mIlaP-_8gkuK1DuaHpD-GGx69DHhNKwztXkVfPQz_nv6GzOeS17j-Jl8cGaK-OVlHpP7nxd321_F9c3l1fb8urBVC6kwnWRtDap1yKSqEF1nDTN9b1Fw4KLlXaV6rupOIkdhhFRONI0VTFiwztXH5Nuhdxf87xVj0vMQLU6TWdCvUYMU2QFruMhodUBtvjoGdHoXhtmERw1M7_3qUe_96r1fzUBnvzn09aV_7Wbs3yKvQjNwdgAw__LPgEFHO-BisR8C2qR7P_yv_xlxNYzR</recordid><startdate>201703</startdate><enddate>201703</enddate><creator>Meyer, Irene</creator><creator>Peter, Tatjana</creator><creator>Batsios, Petros</creator><creator>Kuhnert, Oliver</creator><creator>Krüger-Genge, Anne</creator><creator>Camurça, Carl</creator><creator>Gräf, Ralph</creator><general>Elsevier GmbH</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>201703</creationdate><title>CP39, CP75 and CP91 are major structural components of the Dictyostelium centrosome’s core structure</title><author>Meyer, Irene ; Peter, Tatjana ; Batsios, Petros ; Kuhnert, Oliver ; Krüger-Genge, Anne ; Camurça, Carl ; Gräf, Ralph</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c271t-ab8073197fe0892eefbca0addce6515675b29d593b8e5e6a689f644c606c1cff3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Animals</topic><topic>Centrosome</topic><topic>Centrosome - metabolism</topic><topic>Dictyostelium</topic><topic>Dictyostelium - cytology</topic><topic>Dictyostelium - metabolism</topic><topic>Microtubules</topic><topic>Microtubules - metabolism</topic><topic>Mitosis</topic><topic>Mitosis - physiology</topic><topic>Nucleus</topic><topic>Protozoan Proteins - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Meyer, Irene</creatorcontrib><creatorcontrib>Peter, Tatjana</creatorcontrib><creatorcontrib>Batsios, Petros</creatorcontrib><creatorcontrib>Kuhnert, Oliver</creatorcontrib><creatorcontrib>Krüger-Genge, Anne</creatorcontrib><creatorcontrib>Camurça, Carl</creatorcontrib><creatorcontrib>Gräf, Ralph</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>European journal of cell biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Meyer, Irene</au><au>Peter, Tatjana</au><au>Batsios, Petros</au><au>Kuhnert, Oliver</au><au>Krüger-Genge, Anne</au><au>Camurça, Carl</au><au>Gräf, Ralph</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>CP39, CP75 and CP91 are major structural components of the Dictyostelium centrosome’s core structure</atitle><jtitle>European journal of cell biology</jtitle><addtitle>Eur J Cell Biol</addtitle><date>2017-03</date><risdate>2017</risdate><volume>96</volume><issue>2</issue><spage>119</spage><epage>130</epage><pages>119-130</pages><issn>0171-9335</issn><eissn>1618-1298</eissn><abstract>The acentriolar Dictyostelium centrosome is a nucleus-associated body consisting of a core structure with three plaque-like layers, which are surrounded by a microtubule-nucleating corona. The core duplicates once per cell cycle at the G2/M transition, whereby its central layer disappears and the two outer layers form the mitotic spindle poles. Through proteomic analysis of isolated centrosomes, we have identified CP39 and CP75, two essential components of the core structure. Both proteins can be assigned to the central core layer as their centrosomal presence is correlated to the disappearance and reappearance of the central core layer in the course of centrosome duplication. Both proteins contain domains with centrosome-binding activity in their N- and C-terminal halves, whereby the respective N-terminal half is required for cell cycle-dependent regulation. CP39 is capable of self-interaction and GFP-CP39 overexpression elicited supernumerary microtubule-organizing centers and pre-centrosomal cytosolic clusters. Underexpression stopped cell growth and reversed the MTOC amplification phenotype. In contrast, in case of CP75 underexpression of the protein by RNAi treatment elicited supernumerary MTOCs. In addition, CP75RNAi affects correct chromosome segregation and causes co-depletion of CP39 and CP91, another central core layer component. CP39 and CP75 interact with each other directly in a yeast two-hybrid assay. Furthermore, CP39, CP75 and CP91 mutually interact in a proximity-dependent biotin identification (BioID) assay. Our data indicate that these three proteins are all required for proper centrosome biogenesis and make up the major structural components of core structure's central layer.</abstract><cop>Germany</cop><pub>Elsevier GmbH</pub><pmid>28104305</pmid><doi>10.1016/j.ejcb.2017.01.004</doi><tpages>12</tpages></addata></record> |
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subjects | Animals Centrosome Centrosome - metabolism Dictyostelium Dictyostelium - cytology Dictyostelium - metabolism Microtubules Microtubules - metabolism Mitosis Mitosis - physiology Nucleus Protozoan Proteins - metabolism |
title | CP39, CP75 and CP91 are major structural components of the Dictyostelium centrosome’s core structure |
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