Kubo Tomohiro, Oda Toshiyuki
Department of Anatomy and Structural Biology, Graduate School of Medical Science, University of Yamanashi, Yamanashi 409-3898, Japan.
Mol Biol Cell. 2017 Aug 15;28(17):2260-2266. doi: 10.1091/mbc.E17-05-0285. Epub 2017 Jun 21.
Tubulins undergo various posttranslational modifications. Among them, polyglutamylation is involved in the motility of eukaryotic flagella and the stability of the axonemal microtubules. However, it remains unclear where polyglutamylated tubulin localizes precisely within the axoneme and how tubulin polyglutamylation affects flagellar motility. In this study, we identified the three-dimensional localization of the polyglutamylated tubulin in flagella using antibody labeling and cryo-electron tomography. Polyglutamylated tubulins specifically located in close proximity to a microtubule-cross-bridging structure called the nexin-dynein regulatory complex (N-DRC). Because N-DRC is positively charged, we hypothesized that there is an electrostatic interaction between the polyglutamylated tubulin and the N-DRC, and therefore we mutated the amino acid sequences of DRC4 to modify the charge of the N-DRC. We found that both augmentation and reduction of the positive charge on DRC4 resulted in reduced flagellar motility Moreover, reduced motility in a mutant with a structurally defective N-DRC was partially restored by increasing the positive charge on DRC4. These results clearly indicate that beating motion of flagella is maintained by the electrostatic cross-bridge formed between the negatively charged polyglutamylated tubulins and the positively charged N-DRC.
微管蛋白会经历各种翻译后修饰。其中,多聚谷氨酰胺化参与真核生物鞭毛的运动以及轴丝微管的稳定性。然而,多聚谷氨酰胺化微管蛋白在轴丝内的确切定位以及微管蛋白多聚谷氨酰胺化如何影响鞭毛运动仍不清楚。在本研究中,我们使用抗体标记和冷冻电子断层扫描确定了鞭毛中多聚谷氨酰胺化微管蛋白的三维定位。多聚谷氨酰胺化微管蛋白特异性地定位于一种称为连接蛋白 - 动力蛋白调节复合体(N-DRC)的微管交叉桥结构附近。由于N-DRC带正电荷,我们推测多聚谷氨酰胺化微管蛋白与N-DRC之间存在静电相互作用,因此我们对DRC4的氨基酸序列进行突变以改变N-DRC的电荷。我们发现DRC4上正电荷的增加和减少都会导致鞭毛运动能力下降。此外,通过增加DRC4上的正电荷,具有结构缺陷的N-DRC突变体中降低的运动能力得到了部分恢复。这些结果清楚地表明,鞭毛的摆动运动是由带负电荷的多聚谷氨酰胺化微管蛋白与带正电荷的N-DRC之间形成的静电交叉桥维持的。