Gardner L C, O'Toole E, Perrone C A, Giddings T, Porter M E
Department of Cell Biology and Neuroanatomy, University of Minnesota Medical School, Minneapolis 55455.
J Cell Biol. 1994 Dec;127(5):1311-25. doi: 10.1083/jcb.127.5.1311.
Previous studies of flagellar mutants have identified six axonemal polypeptides as components of a "dynein regulatory complex" (DRC). The DRC is though to coordinate the activity of the multiple flagellar dyneins, but its location within the axoneme has been unknown (Huang et al., 1982; Piperno et al., 1992). We have used improved chromatographic procedures (Kagami and Kamiya, 1992) and computer averaging of EM images (Mastronarde et al., 1992) to analyze the relationship between the DRC and the dynein arms. Our results suggest that some of the DRC components are located at the base of the second radial spoke in close association with the inner dynein arms. (a) Averages of axoneme cross-sections indicate that inner arm structures are significantly reduced in three DRC mutants (pf3 < pf2 < sup-pf-3 < wt). (b) These defects are more pronounced in distal/medial regions of the axoneme than in proximal regions. (c) Analysis of flagellar extracts by fast protein liquid chromatography and SDS-PAGE indicates that a specific dynein I2 isoform is missing in pf3 and reduced in pf2 and sup-pf-3. Comparison with ida4 and pf3ida4 extracts reveals that this isoform differs from those missing in ida4. (d) When viewed in longitudinal section, all three DRC mutants lack a crescent-shaped density above the second radial spoke, and pf3 axonemes lack additional structures adjacent to the crescent. We propose that the crescent corresponds in part to the location of the DRC, and that this structure is also directly associated with a subset of the inner dynein arms. This position is appropriate for a complex that is thought to mediate signals between the radial spokes and the dynein arms.
以往对鞭毛突变体的研究已鉴定出六种轴丝多肽是“动力蛋白调节复合体”(DRC)的组成成分。DRC被认为可协调多种鞭毛动力蛋白的活性,但其在轴丝中的位置一直未知(Huang等人,1982年;Piperno等人,1992年)。我们采用了改进的色谱方法(Kagami和Kamiya,1992年)以及电子显微镜图像的计算机平均技术(Mastronarde等人,1992年)来分析DRC与动力蛋白臂之间的关系。我们的结果表明,一些DRC成分位于第二条径向辐条的基部,与内侧动力蛋白臂紧密相连。(a)轴丝横截面的平均值表明,在三个DRC突变体中内侧臂结构显著减少(pf3 < pf2 < sup-pf-3 < 野生型)。(b)这些缺陷在轴丝的远端/中部区域比近端区域更明显。(c)通过快速蛋白质液相色谱和SDS-PAGE对鞭毛提取物进行分析表明,pf3中一种特定的动力蛋白I2亚型缺失,pf2和sup-pf-3中则减少。与ida4和pf3ida4提取物的比较表明,这种亚型与ida4中缺失的亚型不同。(d)在纵切面上观察时,所有三个DRC突变体在第二条径向辐条上方均缺乏新月形密度,并且pf3轴丝在新月形附近缺乏其他结构。我们提出,新月形部分对应于DRC的位置,并且该结构也与内侧动力蛋白臂的一个子集直接相关。这个位置对于一个被认为在径向辐条和动力蛋白臂之间介导信号的复合体来说是合适的。