Abstract

Inbreeding depression is a widespread phenomenon of central importance to agriculture, medicine, conservation biology and evolutionary biology. Although the population genetic principles of inbreeding depression are well understood, we know little about its functional genomic causes. To provide insight into the molecular interplay between intrinsic stress responses, inbreeding depression and temperature tolerance, we performed a proteomic characterization of a well-defined conditional inbreeding effect in a single line of Drosophila melanogaster, which suffers from extreme cold sensitivity and lethality. We identified 48 differentially expressed proteins in a conditional lethal line as compared to two control lines. These proteins were enriched for proteins involved in hexose metabolism, in particular pyruvate metabolism, and many were found to be associated with lipid particles. These processes can be linked to known cold tolerance mechanisms, such as the production of cryoprotectants, membrane remodeling and the build-up of energy reserves. We checked mRNA-expression of seven genes with large differential protein expression. Although protein expression poorly correlated with gene expression, we found a single gene (CG18067) that, after cold shock, was upregulated in the conditional lethal line both at the mRNA and protein level. Expression of CG18067 also increased in control flies after cold shock, and has previously been linked to cold exposure and chill coma recovery time. Many differentially expressed proteins in our study appear to be involved in cold tolerance in non-inbred individuals. This suggest the conditional inbreeding effect to be caused by misregulation of physiological cold tolerance mechanisms.

Highlights

  • All genomes harbor a number of deleterious mutations that, at the population level, contribute to the genetic load

  • Using a proteomic approach, we have explored an extreme case of cold sensitivity in D. melanogaster, brought about by inbreeding depression

  • We found enrichment for proteins involved in hexose metabolic process and lipid particles, which might function in known cold tolerance mechanisms, such as the production of cryoprotectants, membrane remodeling and the build-up of energy reserves [38]

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Summary

Introduction

All genomes harbor a number of deleterious mutations that, at the population level, contribute to the genetic load. Inbreeding depression can be caused by the decreased expression of heterozygote superiority and by a breakdown of co-adapted gene complexes due to genetic drift. Inbreeding-by-environment (I6E) interactions are a serious threat to long term persistence of populations. It is unclear how, and to what extent, genetic and environmental effects interact in affecting fitness and adaptation in small, isolated populations [7]. To what extent, genetic and environmental effects interact in affecting fitness and adaptation in small, isolated populations [7] This highlights the importance of investigations on environmentally conditioned inbreeding effects

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