A mammalian organelle map by protein correlation profiling

被引:443
|
作者
Foster, LJ
de Hoog, CL
Zhang, YL
Zhang, Y
Xie, XH
Mootha, VK
Mann, M
机构
[1] Univ So Denmark, Dept Biochem & Mol Biol, CEBI, DK-5230 Odense, Denmark
[2] Univ British Columbia, Dept Biochem & Mol Biol, Ctr Proteom, Vancouver, BC V6T 1Z4, Canada
[3] Max Planck Inst Biochem, Dept Proteom & Signal Transduct, D-82152 Martinsried, Germany
[4] Chinese Acad Sci, Beijing Inst Genom, Beijing 101300, Peoples R China
[5] Harvard Univ, Broad Inst, Cambridge, MA 02139 USA
[6] MIT, Cambridge, MA 02139 USA
[7] Harvard Univ, Sch Med, Massachusetts Gen Hosp, Dept Syst Biol, Boston, MA 02115 USA
基金
加拿大健康研究院;
关键词
D O I
10.1016/j.cell.2006.03.022
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Protein localization to membrane-enclosed organelles is a central feature of cellular organization. Using protein correlation profiling, we have mapped 1,404 proteins to ten subcellular locations in mouse liver, and these correspond with enzymatic assays, marker protein profiles, and confocal microscopy. These localizations allowed assessment of the specificity in published organellar proteomic inventories and demonstrate multiple locations for 39% of all organellar proteins. Integration of proteomic and genomic data enabled us to identify networks of coexpressed genes, cis-regulatory motifs, and putative transcriptional regulators involved in organelle biogenesis., Our analysis ties biochemistry, cell biology, and genomics into a common framework for organelle analysis.
引用
收藏
页码:187 / 199
页数:13
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