Abstract

Here we determine the sex-specific influence of mtDNA type (mitotype) and diet on mitochondrial functions and physiology in two Drosophila melanogaster lines. In many species, males and females differ in aspects of their energy production. These sex-specific influences may be caused by differences in evolutionary history and physiological functions. We predicted the influence of mtDNA mutations should be stronger in males than females as a result of the organelle’s maternal mode of inheritance in the majority of metazoans. In contrast, we predicted the influence of diet would be greater in females due to higher metabolic flexibility. We included four diets that differed in their protein: carbohydrate (P:C) ratios as they are the two-major energy-yielding macronutrients in the fly diet. We assayed four mitochondrial function traits (Complex I oxidative phosphorylation, reactive oxygen species production, superoxide dismutase activity, and mtDNA copy number) and four physiological traits (fecundity, longevity, lipid content, and starvation resistance). Traits were assayed at 11 d and 25 d of age. Consistent with predictions we observe that the mitotype influenced males more than females supporting the hypothesis of a sex-specific selective sieve in the mitochondrial genome caused by the maternal inheritance of mitochondria. Also, consistent with predictions, we found that the diet influenced females more than males.

Highlights

  • Sex-specific differences in energy metabolism have motivated research into their evolution and their underlying mechanisms

  • We aim to identify evolutionary and mechanistic sex-specific effects on mitochondrial functions and related physiological traits in two Drosophila melanogaster lines

  • The putative His182Tyr ND2 substitution in Japan mtDNA is predicted to have slightly deleterious implications for proton movement through the ND2 pump. It corresponds to residue 305 in the NuoN subunit for E. coli (Fig 1)

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Summary

Introduction

Sex-specific differences in energy metabolism have motivated research into their evolution and their underlying mechanisms. Sex-specific evolutionary differences are predicted to occur because it is only females that transmit the cellular energy-producing mitochondria, in the majority of species [1]. One clear difference lies in the production and survival of gametes, the sperm, and the egg. Males produce numerous, small, and highly mobile sperm that are disposable. Females produce a small number of large and immobile eggs [2]. While the male shares autosomal and sex-chromosomes, the female provides these chromosomes and cytosolic energy and nutrients for the embryo to develop.

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