Albatross/FBF1 contributes to both centriole duplication and centrosome separation
The centrosome is a small but important organelle that participates in centriole duplication, spindle formation, and ciliogenesis. Each event is regulated by key enzymatic reactions, but how these processes are integrated remains unknown. Recent studies have reported that ciliogenesis is controlled...
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Veröffentlicht in: | Genes to cells : devoted to molecular & cellular mechanisms 2018-12, Vol.23 (12), p.1023-1042 |
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description | The centrosome is a small but important organelle that participates in centriole duplication, spindle formation, and ciliogenesis. Each event is regulated by key enzymatic reactions, but how these processes are integrated remains unknown. Recent studies have reported that ciliogenesis is controlled by distal appendage proteins such as FBF1, also known as Albatross. However, the precise role of Albatross in the centrosome cycle, including centriole duplication and centrosome separation, remains to be determined. Here, we report a novel function for Albatross at the proximal ends of centrioles. Using Albatross monospecific antibodies, full‐length constructs, and siRNAs for rescue experiments, we found that Albatross mediates centriole duplication by recruiting HsSAS‐6, a cartwheel protein of centrioles. Moreover, Albatross participates in centrosome separation during mitosis by recruiting Plk1 to residue S348 of Albatross after its phosphorylation. Taken together, our results show that Albatross is a novel protein that spatiotemporally integrates different aspects of centrosome function, namely ciliogenesis, centriole duplication, and centrosome separation.
Protein–protein interactions involved in the centrosome cycle (Adapted from “Regulating the transition from centriole to basal body”, The Journal of Cell Biology, Vol. 193, No. 3, p436). Full‐length Albatross was confirmed to contribute to ciliation (1), and the C‐terminus and the N‐terminus of Albatross were found to interact with the Plk4‐STIL‐HsSAS‐6 complex and Plk1 for centriole duplication (2) and centrosome separation (3), respectively. |
doi_str_mv | 10.1111/gtc.12648 |
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Protein–protein interactions involved in the centrosome cycle (Adapted from “Regulating the transition from centriole to basal body”, The Journal of Cell Biology, Vol. 193, No. 3, p436). Full‐length Albatross was confirmed to contribute to ciliation (1), and the C‐terminus and the N‐terminus of Albatross were found to interact with the Plk4‐STIL‐HsSAS‐6 complex and Plk1 for centriole duplication (2) and centrosome separation (3), respectively.</description><identifier>ISSN: 1356-9597</identifier><identifier>EISSN: 1365-2443</identifier><identifier>DOI: 10.1111/gtc.12648</identifier><identifier>PMID: 30318703</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>Adaptor Proteins, Signal Transducing - chemistry ; Adaptor Proteins, Signal Transducing - metabolism ; Animals ; cell cycle ; Cell Cycle Proteins - metabolism ; centriole duplication ; Centrioles ; Centrioles - metabolism ; centrosome ; Centrosome - metabolism ; centrosome separation ; cilia ; HEK293 Cells ; HeLa Cells - metabolism ; Humans ; Mice ; Mice, Inbred C57BL ; Mitosis ; NIH 3T3 Cells ; Phosphorylation ; Phosphoserine - metabolism ; Polo-Like Kinase 1 ; Protein Binding ; Protein Domains ; Protein Serine-Threonine Kinases - metabolism ; Proto-Oncogene Proteins - metabolism ; Serine - metabolism ; siRNA</subject><ispartof>Genes to cells : devoted to molecular & cellular mechanisms, 2018-12, Vol.23 (12), p.1023-1042</ispartof><rights>2018 Molecular Biology Society of Japan and John Wiley & Sons Australia, Ltd</rights><rights>2018 Molecular Biology Society of Japan and John Wiley & Sons Australia, Ltd.</rights><rights>Copyright © 2018 Molecular Biology Society of Japan and John Wiley & Sons Australia, Ltd</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4548-acfe115c5a94e81ba6acbf1b30da21023ab12fe050d8c7cef732aaf04db262713</citedby><cites>FETCH-LOGICAL-c4548-acfe115c5a94e81ba6acbf1b30da21023ab12fe050d8c7cef732aaf04db262713</cites><orcidid>0000-0002-6739-2948</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fgtc.12648$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fgtc.12648$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,1427,27901,27902,45550,45551,46384,46808</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30318703$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Inoko, Akihito</creatorcontrib><creatorcontrib>Yano, Tomoki</creatorcontrib><creatorcontrib>Miyamoto, Tatsuo</creatorcontrib><creatorcontrib>Matsuura, Shinya</creatorcontrib><creatorcontrib>Kiyono, Tohru</creatorcontrib><creatorcontrib>Goshima, Naoki</creatorcontrib><creatorcontrib>Inagaki, Masaki</creatorcontrib><creatorcontrib>Hayashi, Yuko</creatorcontrib><title>Albatross/FBF1 contributes to both centriole duplication and centrosome separation</title><title>Genes to cells : devoted to molecular & cellular mechanisms</title><addtitle>Genes Cells</addtitle><description>The centrosome is a small but important organelle that participates in centriole duplication, spindle formation, and ciliogenesis. Each event is regulated by key enzymatic reactions, but how these processes are integrated remains unknown. Recent studies have reported that ciliogenesis is controlled by distal appendage proteins such as FBF1, also known as Albatross. However, the precise role of Albatross in the centrosome cycle, including centriole duplication and centrosome separation, remains to be determined. Here, we report a novel function for Albatross at the proximal ends of centrioles. Using Albatross monospecific antibodies, full‐length constructs, and siRNAs for rescue experiments, we found that Albatross mediates centriole duplication by recruiting HsSAS‐6, a cartwheel protein of centrioles. Moreover, Albatross participates in centrosome separation during mitosis by recruiting Plk1 to residue S348 of Albatross after its phosphorylation. Taken together, our results show that Albatross is a novel protein that spatiotemporally integrates different aspects of centrosome function, namely ciliogenesis, centriole duplication, and centrosome separation.
Protein–protein interactions involved in the centrosome cycle (Adapted from “Regulating the transition from centriole to basal body”, The Journal of Cell Biology, Vol. 193, No. 3, p436). Full‐length Albatross was confirmed to contribute to ciliation (1), and the C‐terminus and the N‐terminus of Albatross were found to interact with the Plk4‐STIL‐HsSAS‐6 complex and Plk1 for centriole duplication (2) and centrosome separation (3), respectively.</description><subject>Adaptor Proteins, Signal Transducing - chemistry</subject><subject>Adaptor Proteins, Signal Transducing - metabolism</subject><subject>Animals</subject><subject>cell cycle</subject><subject>Cell Cycle Proteins - metabolism</subject><subject>centriole duplication</subject><subject>Centrioles</subject><subject>Centrioles - metabolism</subject><subject>centrosome</subject><subject>Centrosome - metabolism</subject><subject>centrosome separation</subject><subject>cilia</subject><subject>HEK293 Cells</subject><subject>HeLa Cells - metabolism</subject><subject>Humans</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mitosis</subject><subject>NIH 3T3 Cells</subject><subject>Phosphorylation</subject><subject>Phosphoserine - metabolism</subject><subject>Polo-Like Kinase 1</subject><subject>Protein Binding</subject><subject>Protein Domains</subject><subject>Protein Serine-Threonine Kinases - metabolism</subject><subject>Proto-Oncogene Proteins - metabolism</subject><subject>Serine - metabolism</subject><subject>siRNA</subject><issn>1356-9597</issn><issn>1365-2443</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kMFLwzAUxoMobk4P_gMS8OShW17StN1xDjeFgSDzHJI01Y6uqUmK7L-3Xac33-U93vfje7wPoVsgU-hq9hH0FGgSZ2doDCzhEY1jdt7PPInmfJ6O0JX3O0KAUcIv0YgRBllK2Bi9LSolg7Pez1aPK8Da1sGVqg3G42CxsuETa9PvbGVw3jZVqWUobY1lnQ-K9XZvsDeNdEflGl0UsvLm5tQn6H31tF0-R5vX9ctysYl0zOMskrowAFxzOY9NBkomUqsCFCO5pEAokwpoYQgneaZTbYqUUSkLEueKJjQFNkH3g2_j7FdrfBA727q6OykocJ6QJMt4Rz0MlO6fdKYQjSv30h0EENGnJ7r0xDG9jr07ObZqb_I_8jeuDpgNwHdZmcP_TmK9XQ6WP_fYeeM</recordid><startdate>201812</startdate><enddate>201812</enddate><creator>Inoko, Akihito</creator><creator>Yano, Tomoki</creator><creator>Miyamoto, Tatsuo</creator><creator>Matsuura, Shinya</creator><creator>Kiyono, Tohru</creator><creator>Goshima, Naoki</creator><creator>Inagaki, Masaki</creator><creator>Hayashi, Yuko</creator><general>Wiley Subscription Services, Inc</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>7TK</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><orcidid>https://orcid.org/0000-0002-6739-2948</orcidid></search><sort><creationdate>201812</creationdate><title>Albatross/FBF1 contributes to both centriole duplication and centrosome separation</title><author>Inoko, Akihito ; Yano, Tomoki ; Miyamoto, Tatsuo ; Matsuura, Shinya ; Kiyono, Tohru ; Goshima, Naoki ; Inagaki, Masaki ; Hayashi, Yuko</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4548-acfe115c5a94e81ba6acbf1b30da21023ab12fe050d8c7cef732aaf04db262713</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Adaptor Proteins, Signal Transducing - chemistry</topic><topic>Adaptor Proteins, Signal Transducing - metabolism</topic><topic>Animals</topic><topic>cell cycle</topic><topic>Cell Cycle Proteins - metabolism</topic><topic>centriole duplication</topic><topic>Centrioles</topic><topic>Centrioles - metabolism</topic><topic>centrosome</topic><topic>Centrosome - metabolism</topic><topic>centrosome separation</topic><topic>cilia</topic><topic>HEK293 Cells</topic><topic>HeLa Cells - metabolism</topic><topic>Humans</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Mitosis</topic><topic>NIH 3T3 Cells</topic><topic>Phosphorylation</topic><topic>Phosphoserine - metabolism</topic><topic>Polo-Like Kinase 1</topic><topic>Protein Binding</topic><topic>Protein Domains</topic><topic>Protein Serine-Threonine Kinases - metabolism</topic><topic>Proto-Oncogene Proteins - metabolism</topic><topic>Serine - metabolism</topic><topic>siRNA</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Inoko, Akihito</creatorcontrib><creatorcontrib>Yano, Tomoki</creatorcontrib><creatorcontrib>Miyamoto, Tatsuo</creatorcontrib><creatorcontrib>Matsuura, Shinya</creatorcontrib><creatorcontrib>Kiyono, Tohru</creatorcontrib><creatorcontrib>Goshima, Naoki</creatorcontrib><creatorcontrib>Inagaki, Masaki</creatorcontrib><creatorcontrib>Hayashi, Yuko</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><jtitle>Genes to cells : devoted to molecular & cellular mechanisms</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Inoko, Akihito</au><au>Yano, Tomoki</au><au>Miyamoto, Tatsuo</au><au>Matsuura, Shinya</au><au>Kiyono, Tohru</au><au>Goshima, Naoki</au><au>Inagaki, Masaki</au><au>Hayashi, Yuko</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Albatross/FBF1 contributes to both centriole duplication and centrosome separation</atitle><jtitle>Genes to cells : devoted to molecular & cellular mechanisms</jtitle><addtitle>Genes Cells</addtitle><date>2018-12</date><risdate>2018</risdate><volume>23</volume><issue>12</issue><spage>1023</spage><epage>1042</epage><pages>1023-1042</pages><issn>1356-9597</issn><eissn>1365-2443</eissn><abstract>The centrosome is a small but important organelle that participates in centriole duplication, spindle formation, and ciliogenesis. Each event is regulated by key enzymatic reactions, but how these processes are integrated remains unknown. Recent studies have reported that ciliogenesis is controlled by distal appendage proteins such as FBF1, also known as Albatross. However, the precise role of Albatross in the centrosome cycle, including centriole duplication and centrosome separation, remains to be determined. Here, we report a novel function for Albatross at the proximal ends of centrioles. Using Albatross monospecific antibodies, full‐length constructs, and siRNAs for rescue experiments, we found that Albatross mediates centriole duplication by recruiting HsSAS‐6, a cartwheel protein of centrioles. Moreover, Albatross participates in centrosome separation during mitosis by recruiting Plk1 to residue S348 of Albatross after its phosphorylation. Taken together, our results show that Albatross is a novel protein that spatiotemporally integrates different aspects of centrosome function, namely ciliogenesis, centriole duplication, and centrosome separation.
Protein–protein interactions involved in the centrosome cycle (Adapted from “Regulating the transition from centriole to basal body”, The Journal of Cell Biology, Vol. 193, No. 3, p436). Full‐length Albatross was confirmed to contribute to ciliation (1), and the C‐terminus and the N‐terminus of Albatross were found to interact with the Plk4‐STIL‐HsSAS‐6 complex and Plk1 for centriole duplication (2) and centrosome separation (3), respectively.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>30318703</pmid><doi>10.1111/gtc.12648</doi><tpages>20</tpages><orcidid>https://orcid.org/0000-0002-6739-2948</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adaptor Proteins, Signal Transducing - chemistry Adaptor Proteins, Signal Transducing - metabolism Animals cell cycle Cell Cycle Proteins - metabolism centriole duplication Centrioles Centrioles - metabolism centrosome Centrosome - metabolism centrosome separation cilia HEK293 Cells HeLa Cells - metabolism Humans Mice Mice, Inbred C57BL Mitosis NIH 3T3 Cells Phosphorylation Phosphoserine - metabolism Polo-Like Kinase 1 Protein Binding Protein Domains Protein Serine-Threonine Kinases - metabolism Proto-Oncogene Proteins - metabolism Serine - metabolism siRNA |
title | Albatross/FBF1 contributes to both centriole duplication and centrosome separation |
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