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Proteome-wide association studies identify biochemical modules associated with a wing-size phenotype in Drosophila melanogaster

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  • Hirokazu Okada

    (Institute of Molecular Systems Biology, ETH Zurich)

  • H. Alexander Ebhardt

    (Institute of Molecular Systems Biology, ETH Zurich)

  • Sibylle Chantal Vonesch

    (Institute of Molecular Systems Biology, ETH Zurich)

  • Ruedi Aebersold

    (Institute of Molecular Systems Biology, ETH Zurich
    Faculty of Science, University of Zurich)

  • Ernst Hafen

    (Institute of Molecular Systems Biology, ETH Zurich
    Faculty of Science, University of Zurich)

Abstract

The manner by which genetic diversity within a population generates individual phenotypes is a fundamental question of biology. To advance the understanding of the genotype–phenotype relationships towards the level of biochemical processes, we perform a proteome-wide association study (PWAS) of a complex quantitative phenotype. We quantify the variation of wing imaginal disc proteomes in Drosophila genetic reference panel (DGRP) lines using SWATH mass spectrometry. In spite of the very large genetic variation (1/36 bp) between the lines, proteome variability is surprisingly small, indicating strong molecular resilience of protein expression patterns. Proteins associated with adult wing size form tight co-variation clusters that are enriched in fundamental biochemical processes. Wing size correlates with some basic metabolic functions, positively with glucose metabolism but negatively with mitochondrial respiration and not with ribosome biogenesis. Our study highlights the power of PWAS to filter functional variants from the large genetic variability in natural populations.

Suggested Citation

  • Hirokazu Okada & H. Alexander Ebhardt & Sibylle Chantal Vonesch & Ruedi Aebersold & Ernst Hafen, 2016. "Proteome-wide association studies identify biochemical modules associated with a wing-size phenotype in Drosophila melanogaster," Nature Communications, Nature, vol. 7(1), pages 1-11, November.
  • Handle: RePEc:nat:natcom:v:7:y:2016:i:1:d:10.1038_ncomms12649
    DOI: 10.1038/ncomms12649
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