Wang Tuanlao, Wong Ka Khuen, Hong Wanjin
Membrane Biology Laboratory, Institute of Molecular and Cell Biology, Singapore 117609, Singapore.
Mol Biol Cell. 2004 Feb;15(2):815-26. doi: 10.1091/mbc.e03-06-0413. Epub 2003 Dec 10.
Rab7 and Rab34 are implicated in regulation of lysosomal morphology and they share a common effector referred to as the RILP (Rab-interacting lysosomal protein). Two novel proteins related to RILP were identified and are tentatively referred to as RLP1 and RLP2 (for RILP-like protein 1 and 2, respectively). Overexpression of RILP caused enlarged lysosomes that are positioned more centrally in the cell. However, the morphology and distribution of lysosomes were not affected by overexpression of either RLP1 or RLP2. The molecular basis for the effect of RILP on lysosomes was investigated, leading to the demonstration that a 62-residue region (amino acids 272-333) of RILP is necessary for RILP's role in regulating lysosomal morphology. Remarkably, transferring this 62-residue region unique to RILP into corresponding sites in RLP1 rendered the chimeric protein capable of regulating lysosome morphology. A correlation between the interaction with GTP-bound form of both Rab proteins and the capability of regulating lysosomes was established. These results define a unique region in RILP responsible for its specific role in regulating lysosomal morphology as well as in its interaction with Rab7 and Rab34.
Rab7和Rab34参与溶酶体形态的调控,它们共有一个被称为RILP(Rab相互作用溶酶体蛋白)的共同效应器。鉴定出了两种与RILP相关的新蛋白,暂称为RLP1和RLP2(分别为类RILP蛋白1和2)。RILP的过表达导致溶酶体增大,且在细胞中定位更靠近中央。然而,RLP1或RLP2的过表达均未影响溶酶体的形态和分布。对RILP影响溶酶体的分子基础进行了研究,结果表明RILP的一个62个残基的区域(氨基酸272 - 333)对于其在调节溶酶体形态中的作用是必需的。值得注意的是,将RILP特有的这个62个残基的区域转移到RLP1的相应位点,使得嵌合蛋白能够调节溶酶体形态。建立了与两种Rab蛋白的GTP结合形式的相互作用和调节溶酶体能力之间的相关性。这些结果确定了RILP中一个独特的区域,该区域负责其在调节溶酶体形态以及与Rab7和Rab34相互作用中的特定作用。