Genetic and environmental perturbations lead to regulatory decoherence

dc.contributor.authorAmanda Lea
dc.contributor.authorMeena Subramaniam
dc.contributor.authorArthur Ko
dc.contributor.authorTerho Lehtimäki
dc.contributor.authorEmma Raitoharju
dc.contributor.authorMika Kähönen
dc.contributor.authorIlkka Seppälä
dc.contributor.authorNina Mononen
dc.contributor.authorOlli T Raitakari
dc.contributor.authorMika Ala-Korpela
dc.contributor.authorPäivi Pajukanta
dc.contributor.authorNoah Zaitlen
dc.contributor.authorJulien F Ayroles
dc.contributor.organizationfi=sydäntutkimuskeskus|en=Cardiovascular Medicine (CAPC)|
dc.contributor.organizationfi=tyks, vsshp|en=tyks, varha|
dc.contributor.organization-code1.2.246.10.2458963.20.35734063924
dc.converis.publication-id39957158
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/39957158
dc.date.accessioned2022-10-28T12:43:46Z
dc.date.available2022-10-28T12:43:46Z
dc.description.abstractCorrelation 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 N MR 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.
dc.identifier.jour-issn2050-084X
dc.identifier.olddbid178545
dc.identifier.oldhandle10024/161639
dc.identifier.urihttps://www.utupub.fi/handle/11111/36051
dc.identifier.urnURN:NBN:fi-fe2021042826288
dc.language.isoen
dc.okm.affiliatedauthorRaitakari, Olli
dc.okm.affiliatedauthorDataimport, tyks, vsshp
dc.okm.discipline1184 Genetics, developmental biology, physiologyen_GB
dc.okm.discipline3121 Internal medicineen_GB
dc.okm.discipline1184 Genetiikka, kehitysbiologia, fysiologiafi_FI
dc.okm.discipline3121 Sisätauditfi_FI
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherELIFE SCIENCES PUBLICATIONS LTD
dc.publisher.countryUnited Kingdomen_GB
dc.publisher.countryBritanniafi_FI
dc.publisher.country-codeGB
dc.relation.articlenumberARTN e40538
dc.relation.doi10.7554/eLife.40538
dc.relation.ispartofjournaleLife
dc.relation.volume8
dc.source.identifierhttps://www.utupub.fi/handle/10024/161639
dc.titleGenetic and environmental perturbations lead to regulatory decoherence
dc.year.issued2019

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