Maternal inheritance, epigenetics and the evolution of polyandry.

Genetica

Department of Biology and Program in Ecology, Evolution and Conservation Biology, University of Nevada, Reno, NV, USA.

Published: September 2008

AI Article Synopsis

  • Growing evidence suggests that females may engage in polyandry to enhance their genetic advantages, either by avoiding compatibility issues or favoring superior male genes.
  • The persistence of variation in male fitness traits, despite traditional "good genes" models of sexual selection, can potentially be explained through non-Mendelian inheritance mechanisms, particularly mitochondrial inheritance and epigenetic regulation.
  • Mitochondrial mutations affect sperm traits and can lead to low sperm quality, while epigenetic changes, influenced by environmental factors, also contribute to heritable variation in male fitness, suggesting that both genetic and environmental factors play crucial roles in reproductive success.

Article Abstract

Growing evidence indicates that females actively engage in polyandry either to avoid genetic incompatibility or to bias paternity in favor of genetically superior males. Despite empirical support for the intrinsic male quality hypothesis, the maintenance of variation in male fitness remains a conundrum for traditional "good genes" models of sexual selection. Here, we discuss two mechanisms of non-Mendelian inheritance, maternal inheritance of mitochondria and epigenetic regulation of gene expression, which may explain the persistence of variation in male fitness traits important in post-copulatory sexual selection. The inability of males to transmit mitochondria precludes any direct evolutionary response to selection on mitochondrial mutations that reduce or enhance male fitness. Consequently, mitochondrial-based variation in sperm traits is likely to persist, even in the face of intense sperm competition. Indeed, mitochondrial nucleotide substitutions, deletions and insertions are now known to be a primary cause of low sperm count and poor sperm motility in humans. Paradoxically, in the field of sexual selection, female-limited response to selection has been largely overlooked. Similarly, the contribution of epigenetics (e.g., DNA methylation, histone modifications and non-coding RNAs) to heritable variation in male fitness has received little attention from evolutionary theorists. Unlike DNA sequence based variation, epigenetic variation can be strongly influenced by environmental and stochastic effects experienced during the lifetime of an individual. Remarkably, in some cases, acquired epigenetic changes can be stably transmitted to offspring. A recent study indicates that sperm exhibit particularly high levels of epigenetic variation both within and between individuals. We suggest that such epigenetic variation may have important implications for post-copulatory sexual selection and may account for recent findings linking sperm competitive ability to offspring fitness.

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Source
http://dx.doi.org/10.1007/s10709-007-9192-zDOI Listing

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