Cargando…
Mating and male pheromone kill Caenorhabditis males through distinct mechanisms
Differences in longevity between sexes is a mysterious yet general phenomenon across great evolutionary distances. To test the roles of responses to environmental cues and sexual behaviors in longevity regulation, we examined Caenorhabditis male lifespan under solitary, grouped, and mated conditions...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5378475/ https://www.ncbi.nlm.nih.gov/pubmed/28290982 http://dx.doi.org/10.7554/eLife.23493 |
_version_ | 1782519450308706304 |
---|---|
author | Shi, Cheng Runnels, Alexi M Murphy, Coleen T |
author_facet | Shi, Cheng Runnels, Alexi M Murphy, Coleen T |
author_sort | Shi, Cheng |
collection | PubMed |
description | Differences in longevity between sexes is a mysterious yet general phenomenon across great evolutionary distances. To test the roles of responses to environmental cues and sexual behaviors in longevity regulation, we examined Caenorhabditis male lifespan under solitary, grouped, and mated conditions. We find that neurons and the germline are required for male pheromone-dependent male death. Hermaphrodites with a masculinized nervous system secrete male pheromone and are susceptible to male pheromone killing. Male pheromone-mediated killing is unique to androdioecious Caenorhabditis, and may reduce the number of males in hermaphroditic populations; neither males nor females of gonochoristic species are susceptible to male pheromone killing. By contrast, mating-induced death, which is characterized by germline-dependent shrinking, glycogen loss, and ectopic vitellogenin expression, utilizes distinct molecular pathways and is shared between the sexes and across species. The study of sex- and species-specific regulation of aging reveals deeply conserved mechanisms of longevity and population structure regulation. DOI: http://dx.doi.org/10.7554/eLife.23493.001 |
format | Online Article Text |
id | pubmed-5378475 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-53784752017-04-05 Mating and male pheromone kill Caenorhabditis males through distinct mechanisms Shi, Cheng Runnels, Alexi M Murphy, Coleen T eLife Developmental Biology and Stem Cells Differences in longevity between sexes is a mysterious yet general phenomenon across great evolutionary distances. To test the roles of responses to environmental cues and sexual behaviors in longevity regulation, we examined Caenorhabditis male lifespan under solitary, grouped, and mated conditions. We find that neurons and the germline are required for male pheromone-dependent male death. Hermaphrodites with a masculinized nervous system secrete male pheromone and are susceptible to male pheromone killing. Male pheromone-mediated killing is unique to androdioecious Caenorhabditis, and may reduce the number of males in hermaphroditic populations; neither males nor females of gonochoristic species are susceptible to male pheromone killing. By contrast, mating-induced death, which is characterized by germline-dependent shrinking, glycogen loss, and ectopic vitellogenin expression, utilizes distinct molecular pathways and is shared between the sexes and across species. The study of sex- and species-specific regulation of aging reveals deeply conserved mechanisms of longevity and population structure regulation. DOI: http://dx.doi.org/10.7554/eLife.23493.001 eLife Sciences Publications, Ltd 2017-03-14 /pmc/articles/PMC5378475/ /pubmed/28290982 http://dx.doi.org/10.7554/eLife.23493 Text en © 2017, Shi et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Developmental Biology and Stem Cells Shi, Cheng Runnels, Alexi M Murphy, Coleen T Mating and male pheromone kill Caenorhabditis males through distinct mechanisms |
title | Mating and male pheromone kill Caenorhabditis males through distinct mechanisms |
title_full | Mating and male pheromone kill Caenorhabditis males through distinct mechanisms |
title_fullStr | Mating and male pheromone kill Caenorhabditis males through distinct mechanisms |
title_full_unstemmed | Mating and male pheromone kill Caenorhabditis males through distinct mechanisms |
title_short | Mating and male pheromone kill Caenorhabditis males through distinct mechanisms |
title_sort | mating and male pheromone kill caenorhabditis males through distinct mechanisms |
topic | Developmental Biology and Stem Cells |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5378475/ https://www.ncbi.nlm.nih.gov/pubmed/28290982 http://dx.doi.org/10.7554/eLife.23493 |
work_keys_str_mv | AT shicheng matingandmalepheromonekillcaenorhabditismalesthroughdistinctmechanisms AT runnelsalexim matingandmalepheromonekillcaenorhabditismalesthroughdistinctmechanisms AT murphycoleent matingandmalepheromonekillcaenorhabditismalesthroughdistinctmechanisms |