Hayashi Shuichi, Shingyoji Chikako
Department of Biological Sciences, Graduate School of Science, University of Tokyo, Hongo, Tokyo 113-0033, Japan.
J Cell Sci. 2008 Sep 1;121(Pt 17):2833-43. doi: 10.1242/jcs.031195. Epub 2008 Aug 5.
Oscillatory movement of eukaryotic flagella is caused by dynein-driven microtubule sliding in the axoneme. The mechanical feedback from the bending itself is involved in the regulation of dynein activity, the main mechanism of which is thought to be switching of the activity of dynein between the two sides of the central pair microtubules. To test this, we developed an experimental system using elastase-treated axonemes of sperm flagella, which have a large Ca(2+)-induced principal bend (P-bend) at the base. On photoreleasing ATP from caged ATP, they slid apart into two bundles of doublets. When the distal overlap region of the slid bundles was bent in the direction opposite to the basal P-bend, backward sliding of the thinner bundle was induced along the flagellum including the bent region. The velocity of the backward sliding was significantly lower than that of the forward sliding, supporting the idea that the dynein activity alternated between the two sides of the central pair on bending. Our results show that the combination of the direction of bending and the conformational state of dynein-microtubule interaction induce the switching of the dynein activity in flagella, thus providing the basis for flagellar oscillation.
真核生物鞭毛的摆动运动是由动力蛋白驱动的轴丝中微管滑动引起的。弯曲本身产生的机械反馈参与动力蛋白活性的调节,其主要机制被认为是中央微管对两侧动力蛋白活性的切换。为了验证这一点,我们开发了一个实验系统,使用经弹性蛋白酶处理的精子鞭毛轴丝,其基部有一个大的钙诱导主弯曲(P弯曲)。当从笼形ATP光释放ATP时,它们滑开形成两束双联微管。当滑动束的远端重叠区域向与基部P弯曲相反的方向弯曲时,较细的束会沿着包括弯曲区域在内的鞭毛向后滑动。向后滑动的速度明显低于向前滑动的速度,这支持了弯曲时中央微管对两侧动力蛋白活性交替的观点。我们的结果表明,弯曲方向和动力蛋白-微管相互作用的构象状态的结合诱导了鞭毛中动力蛋白活性的切换,从而为鞭毛摆动提供了基础。