Cryptic genetic variation of expression quantitative trait locus architecture revealed by genetic perturbation inCaenorhabditis elegans

Author:

van Wijk Marijke H1,Riksen Joost A G1,Elvin Mark2,Poulin Gino B3ORCID,Maulana Muhammad I1,Kammenga Jan E1ORCID,Snoek Basten L4ORCID,Sterken Mark G1ORCID

Affiliation:

1. Laboratory of Nematology, Wageningen University & Research , Droevendaalsesteeg 1, 6708 PB Wageningen , The Netherlands

2. Peak Proteins, Birchwood House, Larkwood Way , Macclesfield, Cheshire, SK10 2XR , UK

3. Division of Molecular and Cellular Function, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester Academic Health Science Centre , Manchester, Oxford Road, M13 9PL , UK

4. Theoretical Biology and Bioinformatics, Utrecht University , 3584 CH Utrecht , The Netherlands

Abstract

AbstractGenetic perturbation in different genetic backgrounds can cause a range of phenotypes within a species. These phenotypic differences can be the result of the interaction between the genetic background and the perturbation. Previously, we reported that perturbation of gld-1, an important player in the developmental control of Caenorhabditis elegans, released cryptic genetic variation (CGV) affecting fitness in different genetic backgrounds. Here, we investigated the change in transcriptional architecture. We found 414 genes with a cis-expression quantitative trait locus (eQTL) and 991 genes with a trans-eQTL that were specifically found in the gld-1 RNAi treatment. In total, we detected 16 eQTL hotspots, of which 7 were only found in the gld-1 RNAi treatment. Enrichment analysis of those 7 hotspots showed that the regulated genes were associated with neurons and the pharynx. Furthermore, we found evidence of accelerated transcriptional aging in the gld-1 RNAi–treated nematodes. Overall, our results illustrate that studying CGV leads to the discovery of hidden polymorphic regulators.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology

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