Microtubule Motors Drive Hedgehog Signaling in Primary Cilia

被引:53
作者
He, Mu [1 ,2 ,3 ]
Agbu, Stephanie [4 ,5 ]
Anderson, Kathryn V. [4 ]
机构
[1] Univ Calif San Francisco, Dept Physiol, San Francisco, CA 94158 USA
[2] Univ Calif San Francisco, Dept Biochem & Biophys, San Francisco, CA 94158 USA
[3] Univ Calif San Francisco, Howard Hughes Med Inst, San Francisco, CA 94158 USA
[4] Mem Sloan Kettering Canc Ctr, Sloan Kettering Inst, Dev Biol Program, 1275 York Ave, New York, NY 10065 USA
[5] Cornell Univ, Biochem Cell & Mol Biol Program, Weill Grad Sch Med Sci, 1300 York Ave, New York, NY 10065 USA
关键词
RIB-POLYDACTYLY SYNDROME; ASPHYXIATING THORACIC DYSTROPHY; COUPLED RECEPTOR GPR161; LEFT-RIGHT ASYMMETRY; IFT-A COMPLEX; INTRAFLAGELLAR TRANSPORT; CYTOPLASMIC DYNEIN; KINESIN-II; DEPOLYMERIZING KINESIN; DYNC2H1; MUTATIONS;
D O I
10.1016/j.tcb.2016.09.010
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The mammalian Hedgehog (Hh) signaling pathway is required for development and for maintenance of adult stem cells, and overactivation of the pathway can cause tumorigenesis. All responses to Hh family ligands in mammals require the primary cilium, an ancient microtubule-based organelle that extends from the cell surface. Genetic studies in mice and humans have defined specific functions for cilium-associated microtubule motor proteins: they act in the construction and disassembly of the primary cilium, they control ciliary length and stability, and some have direct roles in mammalian Hh signal transduction. These studies highlight how integrated genetic and cell biological studies can define the molecular mechanisms that underlie cilium-associated health and disease.
引用
收藏
页码:110 / 125
页数:16
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