The CSC connects three major axonemal complexes involved in dynein regulation

被引:63
|
作者
Heuser, Thomas [1 ]
Dymek, Erin E. [2 ]
Lin, Jianfeng [1 ]
Smith, Elizabeth F. [2 ]
Nicastro, Daniela [1 ]
机构
[1] Brandeis Univ, Rosenstiel Ctr, Dept Biol, Waltham, MA 02454 USA
[2] Dartmouth Coll, Dept Biol Sci, Hanover, NH 03755 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
SLIDING FILAMENT MODEL; RADIAL SPOKE PROTEINS; CRYOELECTRON TOMOGRAPHY; CHLAMYDOMONAS FLAGELLA; WILD-TYPE; MOLECULAR ARCHITECTURE; MICROSCOPE TOMOGRAPHY; ARTIFICIAL MICRORNAS; EUKARYOTIC FLAGELLA; CILIA;
D O I
10.1091/mbc.E12-05-0357
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Motile cilia and flagella are highly conserved organelles that play important roles in human health and development. We recently discovered a calmodulin-and spoke-associated complex (CSC) that is required for wild-type motility and for the stable assembly of a subset of radial spokes. Using cryo-electron tomography, we present the first structure-based localization model of the CSC. Chlamydomonas flagella have two full-length radial spokes, RS1 and RS2, and a shorter RS3 homologue, the RS3 stand-in (RS3S). Using newly developed techniques for analyzing samples with structural heterogeneity, we demonstrate that the CSC connects three major axonemal complexes involved in dynein regulation: RS2, the nexin-dynein regulatory complex (N-DRC), and RS3S. These results provide insights into how signals from the radial spokes may be transmitted to the N-DRC and ultimately to the dynein motors. Our results also indicate that although structurally very similar, RS1 and RS2 likely serve different functions in regulating flagellar motility.
引用
收藏
页码:3143 / 3155
页数:13
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