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Genetic diversity in the BXD panel greatly impacts behavioral, metabolic, and molecular traits.

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posted on 2018-08-09, 18:03 authored by Shanaz Diessler, Maxime Jan, Yann Emmenegger, Nicolas Guex, Benita Middleton, Debra J. Skene, Mark Ibberson, Frederic Burdet, Lou Götz, Marco Pagni, Martial Sankar, Robin Liechti, Charlotte N. Hor, Ioannis Xenarios, Paul Franken

The phenome was divided into 3 phenotypic categories: (i) LMA, (ii) EEG features (labeled EEG), and (iii) sleep-wake state characteristics (labeled State), which were subdivided further (see Materials and methods). The 5 classes of metabolites and the gene expression represent intermediate molecular phenotypic categories. (A) Heritability for EEG/behavioral and metabolite phenotypes. Dots represent single phenotypes within each category and subcategory indicated along the x-axis. Red dots represent phenotypes recorded in baseline (labeled bsl; B1 and B2), blue in recovery (labeled rec; R1 and R2), purple during SD, and green dots refer to the recovery-to-baseline contrasts. Values represent narrow-sense heritability. (B) Overview of significant and highly suggestive (FDR < 0.1) QTLs obtained for all 341 EEG/behavioral phenotypes (phQTLs: LMA in red, EEG in blue, and sleep-wake state in green) and 124 blood metabolite levels in baseline and recovery (mQTLs; purple). Note that overlap of neighboring QTLs renders color shading darker. (C) Venn diagram of genes under significant cis-eQTL effect in liver and cortex for the two experimental conditions (SD and controls [labeled Ctr]). EEG, electroencephalography; eQTL, expression quantitative trait locus; FDR, false discovery rate; LMA, locomotor activity; mQTL, metabolic quantitative trait locus; phQTL, phenotypic quantitative trait locus; QTL, quantitative trait locus; SD, sleep deprivation.

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