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
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