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Cell DOI:10.1016/j.cell.2008.06.016

A mitochondrial protein compendium elucidates complex I disease biology.

Publication TypeJournal Article
Year of Publication2008
AuthorsPagliarini, DJ, Calvo, SE, Chang, B, Sheth, SA, Vafai, SB, Ong, SE, Walford, GA, Sugiana, C, Boneh, A, Chen, WK, Hill, DE, Vidal, M, Evans, JG, Thorburn, DR, Carr, SA, Mootha, VK
JournalCell
Volume134
Issue1
Pages112-23
Date Published2008/07/11
ISSN0092-8674
Abstract

Mitochondria are complex organelles whose dysfunction underlies a broad spectrum of human diseases. Identifying all of the proteins resident in this organelle and understanding how they integrate into pathways represent major challenges in cell biology. Toward this goal, we performed mass spectrometry, GFP tagging, and machine learning to create a mitochondrial compendium of 1098 genes and their protein expression across 14 mouse tissues. We link poorly characterized proteins in this inventory to known mitochondrial pathways by virtue of shared evolutionary history. Using this approach, we predict 19 proteins to be important for the function of complex I (CI) of the electron transport chain. We validate a subset of these predictions using RNAi, including C8orf38, which we further show harbors an inherited mutation in a lethal, infantile CI deficiency. Our results have important implications for understanding CI function and pathogenesis and, more generally, illustrate how our compendium can serve as a foundation for systematic investigations of mitochondria.

URLhttp://linkinghub.elsevier.com/retrieve/pii/S0092-8674(08)00768-X
DOI10.1016/j.cell.2008.06.016
Pubmed

http://www.ncbi.nlm.nih.gov/pubmed/18614015?dopt=Abstract