Edamatsu Masaki
Department of Life Sciences, Graduate School of Arts and Sciences, The University of Tokyo, Tokyo, Japan.
Biochem Biophys Res Commun. 2018 Feb 19;496(4):1382-1388. doi: 10.1016/j.bbrc.2018.02.038. Epub 2018 Feb 6.
Mutational analyses of axonemal dyneins are useful for elucidating the molecular mechanism of ciliary motility. This study demonstrates a mutation system for characterizing lethal P-loop mutations in Tetrahymena outer arm dynein (Dyh3p). The viable DYH3-knockout (vKO-DYH3) cells isolated in this study enabled the examination of lethal mutations in P-loops 1 and 2. The P1 mutant dynein localized in the oral apparatus and the proximal region of the cilia, and the P2 mutant dynein localized only in the oral apparatus. Both results are different from the localization of wild-type Dyh3p. In addition, a co-precipitation assay showed that the P1 and P2 mutant dyneins did not dissociate from microtubules in ATP plus vanadate or in no-ATP conditions, in contrast to wild-type Dyh3p. This mutation system is useful for further molecular studies of axonemal dyneins and ciliary motility.
轴丝动力蛋白的突变分析对于阐明纤毛运动的分子机制很有用。本研究展示了一种用于表征四膜虫外臂动力蛋白(Dyh3p)中致死性P环突变的突变系统。在本研究中分离出的存活的DYH3基因敲除(vKO-DYH3)细胞能够检测P环1和P环2中的致死性突变。P1突变型动力蛋白定位于口器和纤毛的近端区域,而P2突变型动力蛋白仅定位于口器。这两个结果均与野生型Dyh3p的定位不同。此外,共沉淀分析表明,与野生型Dyh3p相比,P1和P2突变型动力蛋白在ATP加钒酸盐或无ATP条件下不会从微管上解离。该突变系统对于轴丝动力蛋白和纤毛运动的进一步分子研究很有用。