Literature DB >> 15665853

SAS-6 defines a protein family required for centrosome duplication in C. elegans and in human cells.

Sebastian Leidel1, Marie Delattre, Lorenzo Cerutti, Karine Baumer, Pierre Gönczy.   

Abstract

The mechanisms that ensure centrosome duplication are poorly understood. In Caenorhabditis elegans, ZYG-1, SAS-4, SAS-5 and SPD-2 are required for centriole formation. However, it is unclear whether these proteins have functional homologues in other organisms. Here, we identify SAS-6 as a component that is required for daughter centriole formation in C. elegans. SAS-6 is a coiled-coil protein that is recruited to centrioles at the onset of the centrosome duplication cycle. Our analysis indicates that SAS-6 and SAS-5 associate and that this interaction, as well as ZYG-1 function, is required for SAS-6 centriolar recruitment. SAS-6 is the founding member of an evolutionarily conserved protein family that contains the novel PISA motif. We investigated the function of the human homologue of SAS-6. GFP-HsSAS-6 localizes to centrosomes and its overexpression results in excess foci-bearing centriolar markers. Furthermore, siRNA-mediated inactivation of HsSAS-6 in U2OS cells abrogates centrosome overduplication following aphidicolin treatment and interferes with the normal centrosome duplication cycle. Therefore, HsSAS-6 is also required for centrosome duplication, indicating that the function of SAS-6-related proteins has been widely conserved during evolution.

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Year:  2005        PMID: 15665853     DOI: 10.1038/ncb1220

Source DB:  PubMed          Journal:  Nat Cell Biol        ISSN: 1465-7392            Impact factor:   28.824


  194 in total

1.  PLK2 phosphorylation is critical for CPAP function in procentriole formation during the centrosome cycle.

Authors:  Jaerak Chang; Onur Cizmecioglu; Ingrid Hoffmann; Kunsoo Rhee
Journal:  EMBO J       Date:  2010-06-08       Impact factor: 11.598

2.  Analysis of centriole elimination during C. elegans oogenesis.

Authors:  Tamara Mikeladze-Dvali; Lukas von Tobel; Petr Strnad; Graham Knott; Heinrich Leonhardt; Lothar Schermelleh; Pierre Gönczy
Journal:  Development       Date:  2012-05       Impact factor: 6.868

3.  Reconstructing the evolutionary history of the centriole from protein components.

Authors:  Matthew E Hodges; Nicole Scheumann; Bill Wickstead; Jane A Langdale; Keith Gull
Journal:  J Cell Sci       Date:  2010-04-13       Impact factor: 5.285

4.  PP2A targets SAS-5 in centriole assembly.

Authors:  Tim Megraw
Journal:  Dev Cell       Date:  2011-04-19       Impact factor: 12.270

5.  Protein phosphatase 2A-SUR-6/B55 regulates centriole duplication in C. elegans by controlling the levels of centriole assembly factors.

Authors:  Mi Hye Song; Yan Liu; D Eric Anderson; Wan Jin Jahng; Kevin F O'Connell
Journal:  Dev Cell       Date:  2011-04-19       Impact factor: 12.270

6.  Regulated HsSAS-6 levels ensure formation of a single procentriole per centriole during the centrosome duplication cycle.

Authors:  Petr Strnad; Sebastian Leidel; Tatiana Vinogradova; Ursula Euteneuer; Alexey Khodjakov; Pierre Gönczy
Journal:  Dev Cell       Date:  2007-08       Impact factor: 12.270

7.  PIPKIγ targets to the centrosome and restrains centriole duplication.

Authors:  Qingwen Xu; Yuxia Zhang; Xunhao Xiong; Yan Huang; Jeffery L Salisbury; Jinghua Hu; Kun Ling
Journal:  J Cell Sci       Date:  2014-01-16       Impact factor: 5.285

8.  Lack of centrioles and primary cilia in STIL(-/-) mouse embryos.

Authors:  Ahuvit David; Fengying Liu; Alexandra Tibelius; Julia Vulprecht; Diana Wald; Ulrike Rothermel; Reut Ohana; Alexander Seitel; Jasmin Metzger; Ruth Ashery-Padan; Hans-Peter Meinzer; Hermann-Josef Gröne; Shai Izraeli; Alwin Krämer
Journal:  Cell Cycle       Date:  2014       Impact factor: 4.534

9.  Centrosome abnormalities during a Chlamydia trachomatis infection are caused by dysregulation of the normal duplication pathway.

Authors:  Kirsten A Johnson; Ming Tan; Christine Sütterlin
Journal:  Cell Microbiol       Date:  2009-03-12       Impact factor: 3.715

Review 10.  Vertebrate maternal-effect genes: Insights into fertilization, early cleavage divisions, and germ cell determinant localization from studies in the zebrafish.

Authors:  Robin E Lindeman; Francisco Pelegri
Journal:  Mol Reprod Dev       Date:  2010-04       Impact factor: 2.609

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