Christensen S T, Guerra C, Wada Y, Valentin T, Angeletti R H, Satir P, Hamasaki T
Departments of Anatomy and Structural Biology and Developmental and Molecular Biology, Albert Einstein College of Medicine of Yeshiva University, Bronx, New York 10461, USA.
J Biol Chem. 2001 Jun 8;276(23):20048-54. doi: 10.1074/jbc.M008412200. Epub 2001 Mar 23.
Ciliary beat frequency is primarily regulated by outer arm dyneins (22 S dynein). Chilcote and Johnson (Chilcote, T. J., and Johnson, K. A. (1990) J. Biol. Chem. 256, 17257-17266) previously studied isolated Tetrahymena 22 S dynein, identifying a protein p34, which showed cAMP-dependent phosphorylation. Here, we characterize the molecular biochemistry of p34 further, demonstrating that it is the functional ortholog of the 22 S dynein regulatory light chain, p29, in Paramecium. p34, thiophosphorylated in isolated axonemes in the presence of cAMP, co-purified with 22 S dynein and not with inner arm dynein (14 S dynein). Isolated 22 S dynein containing phosphorylated p34 showed approximately 70% increase in in vitro microtubule translocation velocity compared with its unphosphorylated counterpart. Extracted p34 rebound to isolated 22 S dynein from either Tetrahymena or Paramecium but not to 14 S dynein from either ciliate. Binding of radiolabeled p34 to 22 S dynein was competitive with p29. Phosphorylated p34 was not present in axonemes isolated from a mutant lacking outer arms. Two-dimensional gel electrophoresis followed by phosphorimaging revealed at least five phosphorylated p34-related spots, consistent with multiple phosphorylation sites in p34 or perhaps multiple isoforms of p34. These new features suggest that a class of outer arm dynein light chains including p34 regulates microtubule sliding velocity and consequently ciliary beat frequency through phosphorylation.
纤毛摆动频率主要由外臂动力蛋白(22S动力蛋白)调节。奇尔科特和约翰逊(奇尔科特,T.J.,和约翰逊,K.A.(1990年)《生物化学杂志》256卷,17257 - 17266页)先前研究了分离的嗜热四膜虫22S动力蛋白,鉴定出一种蛋白p34,它表现出cAMP依赖性磷酸化。在这里,我们进一步表征了p34的分子生物化学,证明它是草履虫中22S动力蛋白调节轻链p29的功能直系同源物。在cAMP存在下,在分离的轴丝中硫代磷酸化的p34与22S动力蛋白共纯化,而不与内臂动力蛋白(14S动力蛋白)共纯化。与未磷酸化的对应物相比,含有磷酸化p34的分离的22S动力蛋白在体外微管转运速度上显示出约70%的增加。从嗜热四膜虫或草履虫中提取的p34能与分离的22S动力蛋白结合,但不能与来自任何一种纤毛虫的14S动力蛋白结合。放射性标记的p34与22S动力蛋白的结合与p29具有竞争性。从缺乏外臂的突变体中分离的轴丝中不存在磷酸化的p34。二维凝胶电泳随后进行磷成像显示至少有五个与磷酸化p34相关的斑点,这与p34中的多个磷酸化位点或可能的p34多种异构体一致。这些新特征表明,包括p34在内的一类外臂动力蛋白轻链通过磷酸化调节微管滑动速度,从而调节纤毛摆动频率。