Abstract

ObjectiveSperm ageing has major evolutionary implications but has received comparatively little attention. Ageing in sperm and other cells is driven largely by oxidative damage from reactive oxygen species (ROS) generated by the mitochondria. Rates of organismal ageing differ across species and are theorized to be linked to somatic ROS levels. However, it is unknown whether sperm ageing rates are correlated with organismal ageing rates. Here, we investigate this question by comparing sperm ROS production in four lines of Drosophila melanogaster that have previously been shown to differ in somatic mitochondrial ROS production, including two commonly used wild-type lines and two lines with genetic modifications standardly used in ageing research.ResultsSomatic ROS production was previously shown to be lower in wild-type Oregon-R than in wild-type Dahomey flies; decreased by the expression of alternative oxidase (AOX), a protein that shortens the electron transport chain; and increased by a loss-of-function mutation in dj-1β, a gene involved in ROS scavenging. Contrary to predictions, we found no differences among these four lines in the rate of sperm ROS production. We discuss the implications of our results, the limitations of our study, and possible directions for future research.

Highlights

  • Like sexually reproducing organisms, sperm cells have a life cycle during which they develop, age, and die

  • Somatic reactive oxygen species (ROS) production was previously shown to be lower in wild-type Oregon-R than in wild-type Dahomey flies; decreased by the expression of alternative oxidase (AOX), a protein that shortens the electron trans‐ port chain; and increased by a loss-of-function mutation in dj-1β, a gene involved in ROS scavenging

  • We found no differences among these four lines in the rate of sperm ROS production

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Summary

Results

Sperm ROS production rates, being non-normally distributed (Shapiro–Wilk normality test, p < 1e−7), were compared using a Kruskal–Wallis rank sum test.

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