Integrated analysis of protein composition, tissue diversity, and gene regulation in mouse mitochondria

被引:708
作者
Mootha, VK
Bunkenborg, J
Olsen, JV
Hjerrild, M
Wisniewski, JR
Stahl, E
Bolouri, MS
Ray, HN
Sihag, S
Kamal, M
Patterson, N
Lander, ES
Mann, M
机构
[1] MIT, Ctr Genome Res, Whitehead Inst, Cambridge, MA 02139 USA
[2] MDS Proteom, DK-5230 Odense, Denmark
[3] Harvard Univ, Sch Med, Brigham & Womens Hosp, Dept Med, Boston, MA 02115 USA
[4] Univ So Denmark, Ctr Expt Bioinformat, DK-5230 Odense, Denmark
[5] MIT, Dept Biol, Cambridge, MA 02138 USA
关键词
D O I
10.1016/S0092-8674(03)00926-7
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
Mitochondria are tailored to meet the metabolic and signaling needs of each cell. To explore its molecular composition, we performed a proteomic survey of mitochondria from mouse brain, heart, kidney, and liver and combined the results with existing gene annotations to produce a list of 591 mitochondrial proteins, including 163 proteins not previously associated with this organelle. The protein expression data were largely concordant with large-scale surveys of RNA abundance and both measures indicate tissue-specific differences in organelle composition. RNA expression profiles across tissues revealed networks of mitochondrial genes that share functional and regulatory mechanisms. We also determined a larger "neighborhood" of genes whose expression is closely correlated to the mitochondrial genes. The combined analysis identifies specific genes of biological interest, such as candidates for mtDNA repair enzymes, offers new insights into the biogenesis and ancestry of mammalian mitochondria, and provides a framework for understanding the organelle's contribution to human disease.
引用
收藏
页码:629 / 640
页数:12
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