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Rab GTPase转运网络的大规模分析:膜组学

Large-scale profiling of Rab GTPase trafficking networks: the membrome.

作者信息

Gurkan Cemal, Lapp Hilmar, Alory Christelle, Su Andrew I, Hogenesch John B, Balch William E

机构信息

Department of Cell Biology, The Scripps Research Institute, La Jolla, CA 92037, USA.

出版信息

Mol Biol Cell. 2005 Aug;16(8):3847-64. doi: 10.1091/mbc.e05-01-0062. Epub 2005 Jun 8.

Abstract

Rab GTPases and SNARE fusion proteins direct cargo trafficking through the exocytic and endocytic pathways of eukaryotic cells. We have used steady state mRNA expression profiling and computational hierarchical clustering methods to generate a global overview of the distribution of Rabs, SNAREs, and coat machinery components, as well as their respective adaptors, effectors, and regulators in 79 human and 61 mouse nonredundant tissues. We now show that this systems biology approach can be used to define building blocks for membrane trafficking based on Rab-centric protein activity hubs. These Rab-regulated hubs provide a framework for an integrated coding system, the membrome network, which regulates the dynamics of the specialized membrane architecture of differentiated cells. The distribution of Rab-regulated hubs illustrates a number of facets that guides the overall organization of subcellular compartments of cells and tissues through the activity of dynamic protein interaction networks. An interactive website for exploring datasets comprising components of the Rab-regulated hubs that define the membrome of different cell and organ systems in both human and mouse is available at http://www.membrome.org/.

摘要

Rab GTP酶和SNARE融合蛋白通过真核细胞的胞吐和胞吞途径指导货物运输。我们利用稳态mRNA表达谱分析和计算层次聚类方法,全面概述了Rabs、SNAREs、包被机制成分及其各自的衔接蛋白、效应蛋白和调节蛋白在79种人类和61种小鼠非冗余组织中的分布情况。我们现在表明,这种系统生物学方法可用于基于以Rab为中心的蛋白质活性中心来定义膜运输的构建模块。这些由Rab调节的中心为一个整合编码系统——膜组网络提供了一个框架,该网络调节分化细胞特化膜结构的动态变化。由Rab调节的中心的分布说明了多个方面,这些方面通过动态蛋白质相互作用网络的活性来指导细胞和组织亚细胞区室的整体组织。可通过http://www.membrome.org/访问一个交互式网站,该网站用于探索包含定义人类和小鼠不同细胞和器官系统膜组的Rab调节中心成分的数据集。

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