Genetic and environmental perturbations lead to regulatory decoherence
Lea, Amanda; Subramaniam, Meena; Ko, Arthur; Lehtimäki, Terho; Raitoharju, Emma; Kähönen, Mika; Seppälä, Ilkka; Mononen, Nina; Raitakari, Olli T.; Ala-Korpela, Mika; Pajukanta, Päivi; Zaitlen, Noah; Ayroles, Julien F. (2019-03-05)
eLife 2019;8:e40538, doi: 10.7554/eLife.40538
© Lea et al. This article is distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use and redistribution provided that the original author and source are credited.
https://creativecommons.org/licenses/by/4.0/
https://urn.fi/URN:NBN:fi-fe202003279478
Tiivistelmä
Abstract
Correlation among traits is a fundamental feature of biological systems that remains difficult to study. To address this problem, we developed a flexible approach that allows us to identify factors associated with inter-individual variation in correlation. We use data from three human cohorts to study the effects of genetic and environmental variation on correlations among mRNA transcripts and among NMR metabolites. We first show that environmental exposures (infection and disease) lead to a systematic loss of correlation, which we define as ‘decoherence’. Using longitudinal data, we show that decoherent metabolites are better predictors of whether someone will develop metabolic syndrome than metabolites commonly used as biomarkers of this disease. Finally, we demonstrate that correlation itself is under genetic control by mapping hundreds of ‘correlation quantitative trait loci (QTLs)’. Together, this work furthers our understanding of how and why coordinated biological processes break down, and points to a potential role for decoherence in disease.
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