A novel Crumbs3 isoform regulates cell division and ciliogenesis via importin β interactions

被引:106
作者
Fan, Shuling
Fogg, Vanessa
Wang, Qian
Chen, Xiao-Wei
Liu, Chia-Jen
Margolis, Ben [1 ]
机构
[1] Univ Michigan, Sch Med, Dept Internal Med, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Sch Med, Dept Biol Chem, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Sch Med, Dept Mol & Integrat Pathol, Ann Arbor, MI 48109 USA
关键词
D O I
10.1083/jcb.200609096
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The Crumbs family of apical transmembrane proteins regulates apicobasal polarity via protein interactions with a conserved C-terminal sequence, ERLI. However, one of the mammalian Crumbs proteins, Crumbs3 (CRB3) has an alternate splice form with a novel C-terminal sequence ending in CLPI (CRB3-CLPI). We report that CRB3-CLPI localizes to the cilia membrane and a membrane compartment at the mitotic spindle poles. Knockdown of CRB3-CLPI leads to both a loss of cilia and a multinuclear phenotype associated with centrosomal and spindle abnormalities. Using protein purification, we find that CRB3-CLPI interacts with importin beta-1 in a Ran-regulated fashion. Importin beta-1 colocalizes with CRB3-CLPI during mitosis, and a dominant-negative form of importin beta-1 closely phenocopies CRB3-CLPI knockdown. Knockdown of importin beta-1 blocks targeting of CRB3-CLPI to the spindle poles. Our data suggest an expanded role for Crumbs proteins in polarized membrane targeting and cell division via unique interactions with importin proteins.
引用
收藏
页码:387 / 398
页数:12
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