β-arrestin-mediated localization of smoothened to the primary cilium

被引:210
作者
Kovacs, Jeffrey J. [1 ,2 ]
Whalen, Erin J. [1 ]
Liu, Renshui [1 ]
Xiao, Kunhong [3 ]
Kim, Jihee [1 ]
Chen, Minyong [1 ]
Wang, Jiangbo [1 ]
Chen, Wei [1 ]
Lefkowitz, Robert J. [1 ,2 ,3 ,4 ]
机构
[1] Duke Univ, Med Ctr, Dept Med, Durham, NC 27710 USA
[2] Duke Univ, Med Ctr, Dept Immunol, Durham, NC 27710 USA
[3] Duke Univ, Med Ctr, Dept Biochem, Durham, NC 27710 USA
[4] Duke Univ, Med Ctr, Howard Hughes Med Inst, Durham, NC 27710 USA
关键词
D O I
10.1126/science.1157983
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
beta-arrestins have important roles in the regulation of seven- transmembrane receptors ( 7TMRs). Smoothened ( Smo) is a 7TMR that mediates effects of Hedgehog on developmental processes and whose dysregulation may cause tumorigenesis. beta-Arrestins are required for endocytosis of Smo and signaling to Gli transcription factors. In mammalian cells, Smo- dependent signaling requires translocation to primary cilia. We demonstrated that beta- arrestins mediate the activity- dependent interaction of Smo and the kinesin motor protein Kif3A. This multimeric complex localized to primary cilia and was disrupted in cells transfected with beta- arrestin small interfering RNA. beta- Arrestin 1 or beta- arrestin 2 depletion prevented the localization of Smo to primary cilia and the Smo- dependent activation of Gli. These results suggest roles for beta- arrestins in mediating the intracellular transport of a 7TMR to its obligate subcellular location for signaling.
引用
收藏
页码:1777 / 1781
页数:5
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