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Biology subjects

Coleen T Murphy

Publications and source records attributed to Coleen T Murphy.

2 recordsLinked to original sources

A simple offspring-to-mother size ratio predicts post-reproductive lifespan

Why do many animals live well beyond their reproductive period? This seems counter to the theory that the fraction of life spent reproducing should be maximized in order to maximize the number of offspring produced in each generation. To resolve this paradox, hypotheses have been developed that evoke parental or grandparental care as reasons for post-reproductive life (e.g., the Mother and Grandmother Hypotheses). However, these hypotheses fail to explain the presence of post-reproductive life in organisms that do not care for their young, such as Caenorhabditis elegans. Here we show that a candidate proxy of the stress of childbirth explains a large portion of the variance in post-reproductive lifespans across many species. A remarkably simple metric, the \"offspring ratio\" (ratio of the size or weight of offspring to that of the mother) explained 77% of the variance of the post-reproductive lifespan in a sample drawn from widely dispersed taxa. Our results suggest that the stress of childbirth is an important and conserved determinant of post-reproductive lifespan. Thus, long post-reproductive lifespan may simply be a byproduct of the somatic health required for reproduction of large progeny, regardless of parental care.

Genetics

Mating-induced Male Death and Pheromone Toxin-regulated Androstasis

How mating affects male lifespan is poorly understood. Using single worm lifespan assays, we discovered that males live significantly shorter after mating in both androdioecious (male and hermaphroditic) and gonochoristic (male and female) Caenorhabditis. Germline-dependent shrinking, glycogen loss, and ectopic expression of vitellogenins contribute to male post-mating lifespan reduction, which is conserved between the sexes. In addition to mating-induced lifespan decrease, worms are subject to killing by male pheromone-dependent toxicity. C. elegans males are the most sensitive, whereas C. remanei are immune, suggesting that males in androdioecious and gonochoristic species utilize male pheromone differently as a toxin or a chemical messenger. Our study reveals two mechanisms involved in male lifespan regulation: germline-dependent shrinking and death is the result of an unavoidable cost of reproduction and is evolutionarily conserved, whereas male pheromone-mediated killing provides a novel mechanism to cull the male population and ensure a return to the self-reproduction mode in androdioecious species. Our work highlights the importance of understanding the shared vs. sex- and species-specific mechanisms that regulate lifespan.

Genetics