Department of Biological Sciences, Dartmouth College, Hanover, New Hampshire 03755, USA.
Cytoskeleton (Hoboken). 2012 Mar;69(3):179-94. doi: 10.1002/cm.21010. Epub 2012 Feb 8.
Numerous studies have indicated that each of the seven projections associated with the central pair of microtubules plays a distinct role in regulating eukaryotic ciliary/flagellar motility. Mutants which lack specific projections have distinct motility phenotypes. For example, Chlamydomonas pf6 mutants lack the C1a projection and have twitchy, non-beating flagella. The C1a projection is a complex of proteins including PF6, C1a-86, C1a-34, C1a-32, C1a-18, and calmodulin. To define functional domains within PF6 and to potentially assign functions to specific C1a components, we generated deletion constructs of the PF6 gene and tested for their ability to assemble and rescue motility upon transformation of mutant pf6 cells. Our results demonstrate that domains near the carboxyl-terminus of PF6 are essential for motility and/or assembly of the projection. The amino terminal half of PF6 is not required for C1a assembly; however, this region is important for stability of the C1a-34, C1a-32, and C1a-18 sub-complex and wild-type beat frequency. Analysis of double mutants lacking the amino terminus of PF6 and outer dynein arms reveal that C1a may play a role in modulating both inner and outer dynein arm activity.
许多研究表明,与中央对微管相关的七个突起中的每一个在调节真核纤毛/鞭毛运动方面都起着独特的作用。缺乏特定突起的突变体具有不同的运动表型。例如,眼虫 pf6 突变体缺乏 C1a 突起,具有抽搐、不跳动的鞭毛。C1a 突起是包括 PF6、C1a-86、C1a-34、C1a-32、C1a-18 和钙调蛋白在内的蛋白质复合物。为了确定 PF6 内的功能域,并可能为特定的 C1a 成分分配功能,我们生成了 PF6 基因的缺失构建体,并测试了它们在转化突变体 pf6 细胞后组装和恢复运动的能力。我们的结果表明,PF6 羧基末端附近的结构域对于突起的运动和/或组装是必需的。PF6 的氨基末端一半对于 C1a 的组装不是必需的;然而,该区域对于 C1a-34、C1a-32 和 C1a-18 亚复合物以及野生型拍打频率的稳定性很重要。分析缺乏 PF6 和外动力蛋白臂氨基末端的双突变体表明,C1a 可能在调节内动力蛋白臂和外动力蛋白臂的活性方面发挥作用。