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本文引用的文献

1
Lysosomal cysteine proteases regulate antigen presentation.溶酶体半胱氨酸蛋白酶调节抗原呈递。
Nat Rev Immunol. 2003 Jun;3(6):472-82. doi: 10.1038/nri1110.
2
Use of expression constructs to dissect the functional domains of the CHS/beige protein: identification of multiple phenotypes.利用表达构建体剖析CHS/米色蛋白的功能结构域:多种表型的鉴定。
Traffic. 2003 Jun;4(6):403-15. doi: 10.1034/j.1600-0854.2003.00093.x.
3
The role of microscopy in understanding atherosclerotic lysosomal lipid metabolism.显微镜检查在理解动脉粥样硬化溶酶体脂质代谢中的作用。
Microsc Microanal. 2003 Feb;9(1):54-67. doi: 10.1017/S1431927603030010.
4
Interorganellar regulation of lysosome positioning by the Golgi apparatus through Rab34 interaction with Rab-interacting lysosomal protein.高尔基体通过Rab34与Rab相互作用溶酶体蛋白的相互作用对溶酶体定位进行细胞器间调控。
Mol Biol Cell. 2002 Dec;13(12):4317-32. doi: 10.1091/mbc.e02-05-0280.
5
Enzyme replacement and enhancement therapies: lessons from lysosomal disorders.酶替代和增强疗法:溶酶体贮积症的经验教训。
Nat Rev Genet. 2002 Dec;3(12):954-66. doi: 10.1038/nrg963.
6
[Lysosomes and lysosomal storage diseases].[溶酶体与溶酶体贮积症]
J Soc Biol. 2002;196(2):127-34.
7
Chediak-Higashi syndrome: a clinical and molecular view of a rare lysosomal storage disorder.切迪阿克-希加什综合征:一种罕见的溶酶体贮积症的临床与分子视角
Curr Mol Med. 2002 Aug;2(5):469-77. doi: 10.2174/1566524023362339.
8
Chediak-Higashi Syndrome: a rare disorder of lysosomes and lysosome related organelles.切-东综合征:一种罕见的溶酶体及溶酶体相关细胞器疾病。
Pigment Cell Res. 2002 Aug;15(4):251-7. doi: 10.1034/j.1600-0749.2002.02038.x.
9
The dark side of lysosome-related organelles: specialization of the endocytic pathway for melanosome biogenesis.溶酶体相关细胞器的阴暗面:黑素小体生物发生的内吞途径特化
Traffic. 2002 Apr;3(4):237-48. doi: 10.1034/j.1600-0854.2002.030401.x.
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A view to a kill: signals triggering cytotoxicity.致命一击:触发细胞毒性的信号
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RILP的一个独特区域使其在溶酶体形态调节以及与Rab7和Rab34的相互作用方面有别于其相关蛋白。

A unique region of RILP distinguishes it from its related proteins in its regulation of lysosomal morphology and interaction with Rab7 and Rab34.

作者信息

Wang Tuanlao, Wong Ka Khuen, Hong Wanjin

机构信息

Membrane Biology Laboratory, Institute of Molecular and Cell Biology, Singapore 117609, Singapore.

出版信息

Mol Biol Cell. 2004 Feb;15(2):815-26. doi: 10.1091/mbc.e03-06-0413. Epub 2003 Dec 10.

DOI:10.1091/mbc.e03-06-0413
PMID:14668488
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC329395/
Abstract

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.

摘要

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。