Systems proteomics of liver mitochondria function

Author:

Williams Evan G.12,Wu Yibo32,Jha Pooja1,Dubuis Sébastien3,Blattmann Peter3,Argmann Carmen A.4,Houten Sander M.4,Amariuta Tiffany1,Wolski Witold3,Zamboni Nicola3,Aebersold Ruedi35,Auwerx Johan1

Affiliation:

1. Laboratory of Integrative and Systems Physiology, Interfaculty Institute of Bioengineering, École Polytechnique Fédérale de Lausanne, CH-1015, Switzerland.

2. These authors contributed equally to this work.

3. Department of Biology, Institute of Molecular Systems Biology, ETH Zurich, CH-8093, Switzerland.

4. Department of Genetics and Genomic Sciences and Icahn Institute for Genomics and Multiscale Biology, Icahn School of Medicine at Mount Sinai, 1425 Madison Avenue, Box 1498, New York, NY 10029, USA.

5. Faculty of Science, University of Zurich, CH-8057, Switzerland.

Abstract

Expanded proteomic analysis of metabolism Combined analysis of large data sets characterizing genes, transcripts, and proteins can elucidate biological functions and disease processes. Williams et al. report an exceptionally detailed characterization of mitochondrial function in a genetic reference panel of recombinant inbred mice. They measured the metabolic function of nearly 400 mice under various environmental conditions and collected detailed quantitative information from livers of the animals on over 25,000 transcripts. These data were integrated with quantitation of over 2500 proteins and nearly 1000 metabolites. Such analysis showed a frequent lack of correlation of transcript and protein abundance, enabled the identification of genomic variants of mitochondrial enzymes that caused inborn errors in metabolism, and revealed two genes that appear to function in cholesterol metabolism. Science , this issue p. 10.1126/science.aad0189

Funder

EPFL

ETHZ

ERC

Swiss Initiative for Systems Biology

SNSF

NIH

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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