Polarity proteins control ciliogenesis via kinesin motor interactions

被引:178
作者
Fan, SL
Hurd, TW
Liu, CJ
Straight, SW
Weimbs, T
Hurd, EA
Domino, SE
Margolis, B [1 ]
机构
[1] Univ Michigan, Howard Hughes Med Inst, Sch Med, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Internal Med, Sch Med, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Dept Obstet & Gynaecol, Sch Med, Cellular & Mol Biol Program, Ann Arbor, MI 48109 USA
[4] Univ Michigan, Dept Biol Chem, Sch Med, Ann Arbor, MI 48109 USA
[5] Cleveland Clin, Dept Cell Biol, Lerner Res Inst, Cleveland, OH 44195 USA
[6] Cleveland Clin, Glickman Urol Inst, Cleveland, OH 44195 USA
关键词
D O I
10.1016/j.cub.2004.08.025
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: Cilia are specialized organelles that play a fundamental role in several mammalian processes including left-right axis determination, sperm motility, and photoreceptor maintenance. Mutations in cilia-localized proteins have been linked to human diseases including cystic kidney disease and retinitis pigmentosa. Retinitis pigmentosa can be caused by loss-of-function mutations in the polarity protein Crumbs1 (CRB1), but the exact role of CRB1 in retinal function is unclear. Results: Here we show that CRB3, a CRB1 -related protein found in epithelia, is localized to cilia and required for proper cilia formation. We also find that the Crumbs-associated Par3/Par6/aPKC polarity cassette localizes to cilia and regulates ciliogenesis. In addition, there appears to be an important role for the polarity-regulating 14-3-3 proteins in this process. Finally, we can demonstrate association of these polarity proteins with microtubules and the microtubular motor KIF3/Kinesin-II. Conclusions: Our findings point to a heretofore unappreciated role for polarity proteins in cilia formation and provide a potentially unique insight into the pathogenesis of human kidney and retinal disease.
引用
收藏
页码:1451 / 1461
页数:11
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