PPP1R35 ensures centriole homeostasis by promoting centriole-to-centrosome conversion

被引:10
作者
Fong, Chii Shyang [1 ]
Ozaki, Kanako [1 ]
Tsou, Meng-Fu Bryan [1 ,2 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Cell Biol Program, New York, NY 10065 USA
[2] Cornell Univ, Weill Cornell Grad Sch Med Sci, New York, NY 10065 USA
基金
美国国家卫生研究院;
关键词
DUPLICATION; DOCKING; POLO;
D O I
10.1091/mbc.E18-08-0525
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Centriole-to-centrosome conversion (CCC) safeguards centriole homeostasis by coupling centriole duplication with segregation, and is essential for stabilization of mature vertebrate centrioles naturally devoid of the geometric scaffold or the cartwheel. Here we identified PPP1R35, a putative regulator of the protein phosphatase PP1, as a novel centriolar protein required for CCC. We found that PPP1R35 is enriched at newborn daughter centrioles in S or G2 phase. In the absence of PPP1R35, centriole assembly initiates normally in S phase, but none of the nascent centrioles can form active centrosomes or recruit CEP295, an essential factor for CCC. Instead, all PPP1R35-null centrioles, although stable during their birth in interphase, become disintegrated after mitosis upon cartwheel removal. Surprisingly, we found that neither the centriolar localization nor the function of PPP1R35 in CCC requires the putative PP1-interacting motif. PPP1R35 is thus acting upstream of CEP295 to induce CCC for proper centriole maintenance.
引用
收藏
页码:2801 / 2808
页数:8
相关论文
共 18 条
[1]   CEP295 interacts with microtubules and is required for centriole elongation [J].
Chang, Ching-Wen ;
Hsu, Wen-Bin ;
Tsai, Jhih-Jie ;
Tang, Chieh-Ju C. ;
Tang, Tang K. .
JOURNAL OF CELL SCIENCE, 2016, 129 (13) :2501-2513
[2]   Identification of the human testis protein phosphatase 1 interactome [J].
Fardilha, Margarida ;
Esteves, Sara L. C. ;
Korrodi-Gregorio, Luis ;
Vintem, Ana Paula ;
Domingues, Sara C. ;
Rebelo, Sandra ;
Morrice, Nick ;
Cohen, Patricia T. W. ;
da Cruz e Silva, Odete A. B. ;
da Cruz e Silva, Edgar F. .
BIOCHEMICAL PHARMACOLOGY, 2011, 82 (10) :1403-1415
[3]   Conserved molecular interactions in centriole-to-centrosome conversion [J].
Fu, Jingyan ;
Lipinszki, Zoltan ;
Rangone, Helene ;
Min, Mingwei ;
Mykura, Charlotte ;
Chao-Chu, Jennifer ;
Schneider, Sandra ;
Dzhindzhev, Nikola S. ;
Gottardo, Marco ;
Riparbelli, Maria Giovanna ;
Callaini, Giuliano ;
Glover, David M. .
NATURE CELL BIOLOGY, 2016, 18 (01) :87-+
[4]   Docking Motif-Guided Mapping of the Interactome of Protein Phosphatase-1 [J].
Hendrickx, Annick ;
Beullens, Monique ;
Ceulemans, Hugo ;
Den Abt, Tom ;
Van Eynde, Aleyde ;
Nicolaescu, Emilia ;
Lesage, Bart ;
Bollen, Mathieu .
CHEMISTRY & BIOLOGY, 2009, 16 (04) :365-371
[5]   Stabilization of Cartwheel-less Centrioles for Duplication Requires CEP295-Mediated Centriole-to-Centrosome Conversion [J].
Izquierdo, Denisse ;
Wang, Won-Jing ;
Uryu, Kunihiro ;
Tsou, Meng-Fu Bryan .
CELL REPORTS, 2014, 8 (04) :957-965
[6]   Novel asymmetrically localizing components of human centrosomes identified by complementary proteomics methods [J].
Jakobsen, Lis ;
Vanselow, Katja ;
Skogs, Marie ;
Toyoda, Yusuke ;
Lundberg, Emma ;
Poser, Ina ;
Falkenby, Lasse G. ;
Bennetzen, Martin ;
Westendorf, Jens ;
Nigg, Erich A. ;
Uhlen, Mathias ;
Hyman, Anthony A. ;
Andersen, Jens S. .
EMBO JOURNAL, 2011, 30 (08) :1520-1535
[7]   Promotion and Suppression of Centriole Duplication Are Catalytically Coupled through PLK4 to Ensure Centriole Homeostasis [J].
Kim, Minhee ;
O'Rourke, Brian P. ;
Soni, Rajesh Kumar ;
Jallepalli, Prasad V. ;
Hendrickson, Ronald C. ;
Tsou, Meng-Fu Bryan .
CELL REPORTS, 2016, 16 (05) :1195-1203
[8]   RNA-Guided Human Genome Engineering via Cas9 [J].
Mali, Prashant ;
Yang, Luhan ;
Esvelt, Kevin M. ;
Aach, John ;
Guell, Marc ;
DiCarlo, James E. ;
Norville, Julie E. ;
Church, George M. .
SCIENCE, 2013, 339 (6121) :823-826
[9]   Cdk1 Phosphorylates Drosophila Sas-4 to Recruit Polo to Daughter Centrioles and Convert Them to Centrosomes [J].
Novak, Zsofia A. ;
Wainman, Alan ;
Gartenmann, Lisa ;
Raff, Jordan W. .
DEVELOPMENTAL CELL, 2016, 37 (06) :545-557
[10]   Combination of Chemical Genetics and Phosphoproteomics for Kinase Signaling Analysis Enables Confident Identification of Cellular Downstream Targets [J].
Oppermann, Felix S. ;
Grundner-Culemann, Kathrin ;
Kumar, Chanchal ;
Gruss, Oliver J. ;
Jallepalli, Prasad V. ;
Daub, Henrik .
MOLECULAR & CELLULAR PROTEOMICS, 2012, 11 (04)