Departments of Cell Biology and Biophysics, University of Texas Southwestern Medical Center, Dallas, TX 75235.
Laboratory of Cytoskeleton and Cilia Biology, Department of Cell Biology, Nencki Institute of Experimental Biology of Polish Academy of Sciences, 02-093 Warsaw, Poland.
Mol Biol Cell. 2018 May 1;29(9):1048-1059. doi: 10.1091/mbc.E18-02-0142. Epub 2018 Mar 22.
Motile cilia are essential for propelling cells and moving fluids across tissues. The activity of axonemal dynein motors must be precisely coordinated to generate ciliary motility, but their regulatory mechanisms are not well understood. The tether and tether head (T/TH) complex was hypothesized to provide mechanical feedback during ciliary beating because it links the motor domains of the regulatory I1 dynein to the ciliary doublet microtubule. Combining genetic and biochemical approaches with cryoelectron tomography, we identified FAP44 and FAP43 (plus the algae-specific, FAP43-redundant FAP244) as T/TH components. WT-mutant comparisons revealed that the heterodimeric T/TH complex is required for the positional stability of the I1 dynein motor domains, stable anchoring of CK1 kinase, and proper phosphorylation of the regulatory IC138-subunit. T/TH also interacts with inner dynein arm d and radial spoke 3, another important motility regulator. The T/TH complex is a conserved regulator of I1 dynein and plays an important role in the signaling pathway that is critical for normal ciliary motility.
纤毛的运动对于推动细胞和在组织间移动液体至关重要。轴丝动力蛋白的活性必须精确协调,才能产生纤毛运动,但它们的调节机制尚不清楚。推测系留蛋白和系留头(T/TH)复合物在纤毛摆动时提供机械反馈,因为它将调节型 I1 动力蛋白的马达结构域与纤毛二联体微管连接起来。通过将遗传和生化方法与冷冻电镜断层扫描相结合,我们鉴定出 FAP44 和 FAP43(以及藻类特有的、冗余的 FAP244)为 T/TH 复合物的组成部分。WT-突变体比较表明,异二聚体 T/TH 复合物对于 I1 动力蛋白的位置稳定性、CK1 激酶的稳定锚定以及调节 IC138 亚基的正确磷酸化是必需的。T/TH 还与内动力蛋白臂 d 和另一个重要的运动调节剂径向辐条 3 相互作用。T/TH 复合物是 I1 动力蛋白的保守调节剂,在对正常纤毛运动至关重要的信号通路中发挥重要作用。