Kinesin-3 KLP-6 Regulates Intraflagellar Transport in Male-Specific Cilia of Caenorhabditis elegans

被引:47
|
作者
Morsci, Natalia S. [1 ,2 ]
Barr, Maureen M. [1 ]
机构
[1] Rutgers State Univ, Dept Genet, Piscataway, NJ 08854 USA
[2] Univ Wisconsin, Cell & Mol Biol Program, Madison, WI 53706 USA
基金
美国国家卫生研究院;
关键词
C-ELEGANS; SENSORY CILIA; IFT PARTICLES; MOTOR PROTEIN; CHLAMYDOMONAS; MECHANISMS; MOTILITY; FLAGELLA; NEURONS; DISEASE;
D O I
10.1016/j.cub.2011.06.027
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
Cilia are cellular sensory organelles whose integrity of structure and function are important to human health [1]. All cilia are assembled and maintained by kinesin-2 motors in a process termed intraflagellar transport (IFT), but they exhibit great variety of morphology and function. This diversity is proposed to be conferred by cell-specific modulation of the core IFT by additional factors, but examples of such IFT modulators are limited [2-4]. Here we demonstrate that the cell-specific kinesin-3 KLP-6 acts as a modulator of both IFT dynamics and length in the cephalic male (CEM) cilia of Caenorhabditis elegans. Live imaging of GFP-tagged kinesins in CEM cilia shows partial uncoupling of the IFT motors of the kinesin-2 family, kinesin-II and OSM-3/KIF17, with a portion of OSM-3 moving independently of the IFT complex. KLP-6 moves independently of the kinesin-2 motors and acts to reduce the velocity of OSM-3 and IFT. Additionally, kinesin-II mutants display a novel CEM cilia elongation phenotype that is partially dependent on OSM-3 and KLP-6. Our observations illustrate modulation of the general kinesin-2-driven IFT process by a cell-specific kinesin-3 in cilia of C. elegans male neurons.
引用
收藏
页码:1239 / 1244
页数:6
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