Bae C D, Min D S, Fleming I N, Exton J H
Howard Hughes Medical Institute and the Department of Molecular Physiology and Biophysics, Vanderbilt University School of Medicine, Nashville, Tennessee 37232, USA.
J Biol Chem. 1998 May 8;273(19):11596-604. doi: 10.1074/jbc.273.19.11596.
Phospholipase D (PLD) has been identified as a target of small G proteins of the Rho family. The present study was directed at defining the interaction sites of RhoA with rat brain PLD in vitro using chimeric proteins between RhoA and Ha-Ras or Cdc42Hs and point mutations. The switch I region of RhoA, which is the common effector domain of Ras-like G proteins, was a crucial interaction site for PLD. Mutations in conserved amino acids (Tyr34, Thr37, Phe39) totally abolished PLD activation, while mutations in Val38 or Tyr42 caused partial loss. Two additional sites were responsible for the differential PLD activation ability between RhoA and Cdc42Hs. Changing Asp76 in the switch II region of RhoA to the corresponding amino acid in Cdc42Hs led to partial loss of PLD activation. A chimeric protein with the N-terminal third of Cdc42Hs changed to RhoA showed enhanced PLD activation. Analysis of other Rho/Ha-Ras chimeric proteins and mutations indicated that Gln52 adjacent to the switch II region is responsible for this gain of function. In conclusion, the present study shows that conserved amino acids in the switch I region of RhoA are major PLD interaction sites and that residues in the switch II and internal regions are responsible for the differential activation of PLD by RhoA and Cdc42Hs.
磷脂酶D(PLD)已被确定为Rho家族小G蛋白的一个靶点。本研究旨在利用RhoA与Ha-Ras或Cdc42Hs之间的嵌合蛋白以及点突变,在体外确定RhoA与大鼠脑PLD的相互作用位点。RhoA的开关I区域是Ras样G蛋白的共同效应结构域,是PLD的关键相互作用位点。保守氨基酸(Tyr34、Thr37、Phe39)的突变完全消除了PLD的激活,而Val38或Tyr42的突变导致部分丧失激活能力。另外两个位点导致了RhoA和Cdc42Hs之间PLD激活能力的差异。将RhoA开关II区域的Asp76替换为Cdc42Hs中的相应氨基酸导致PLD激活部分丧失。一种将Cdc42Hs N端三分之一替换为RhoA的嵌合蛋白显示出增强的PLD激活。对其他Rho/Ha-Ras嵌合蛋白和突变的分析表明,开关II区域附近的Gln52负责这种功能获得。总之,本研究表明,RhoA开关I区域中的保守氨基酸是主要的PLD相互作用位点,开关II区域和内部区域的残基负责RhoA和Cdc42Hs对PLD的差异激活。