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Wild worm embryogenesis harbors ubiquitous polygenic modifier variation
Embryogenesis is an essential and stereotypic process that nevertheless evolves among species. Its essentiality may favor the accumulation of cryptic genetic variation (CGV) that has no effect in the wild-type but that enhances or suppresses the effects of rare disruptions to gene function. Here, we...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4569889/ https://www.ncbi.nlm.nih.gov/pubmed/26297805 http://dx.doi.org/10.7554/eLife.09178 |
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author | Paaby, Annalise B White, Amelia G Riccardi, David D Gunsalus, Kristin C Piano, Fabio Rockman, Matthew V |
author_facet | Paaby, Annalise B White, Amelia G Riccardi, David D Gunsalus, Kristin C Piano, Fabio Rockman, Matthew V |
author_sort | Paaby, Annalise B |
collection | PubMed |
description | Embryogenesis is an essential and stereotypic process that nevertheless evolves among species. Its essentiality may favor the accumulation of cryptic genetic variation (CGV) that has no effect in the wild-type but that enhances or suppresses the effects of rare disruptions to gene function. Here, we adapted a classical modifier screen to interrogate the alleles segregating in natural populations of Caenorhabditis elegans: we induced gene knockdowns and used quantitative genetic methodology to examine how segregating variants modify the penetrance of embryonic lethality. Each perturbation revealed CGV, indicating that wild-type genomes harbor myriad genetic modifiers that may have little effect individually but which in aggregate can dramatically influence penetrance. Phenotypes were mediated by many modifiers, indicating high polygenicity, but the alleles tend to act very specifically, indicating low pleiotropy. Our findings demonstrate the extent of conditional functionality in complex trait architecture. DOI: http://dx.doi.org/10.7554/eLife.09178.001 |
format | Online Article Text |
id | pubmed-4569889 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-45698892015-09-17 Wild worm embryogenesis harbors ubiquitous polygenic modifier variation Paaby, Annalise B White, Amelia G Riccardi, David D Gunsalus, Kristin C Piano, Fabio Rockman, Matthew V eLife Genomics and Evolutionary Biology Embryogenesis is an essential and stereotypic process that nevertheless evolves among species. Its essentiality may favor the accumulation of cryptic genetic variation (CGV) that has no effect in the wild-type but that enhances or suppresses the effects of rare disruptions to gene function. Here, we adapted a classical modifier screen to interrogate the alleles segregating in natural populations of Caenorhabditis elegans: we induced gene knockdowns and used quantitative genetic methodology to examine how segregating variants modify the penetrance of embryonic lethality. Each perturbation revealed CGV, indicating that wild-type genomes harbor myriad genetic modifiers that may have little effect individually but which in aggregate can dramatically influence penetrance. Phenotypes were mediated by many modifiers, indicating high polygenicity, but the alleles tend to act very specifically, indicating low pleiotropy. Our findings demonstrate the extent of conditional functionality in complex trait architecture. DOI: http://dx.doi.org/10.7554/eLife.09178.001 eLife Sciences Publications, Ltd 2015-08-22 /pmc/articles/PMC4569889/ /pubmed/26297805 http://dx.doi.org/10.7554/eLife.09178 Text en © 2015, Paaby 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 | Genomics and Evolutionary Biology Paaby, Annalise B White, Amelia G Riccardi, David D Gunsalus, Kristin C Piano, Fabio Rockman, Matthew V Wild worm embryogenesis harbors ubiquitous polygenic modifier variation |
title | Wild worm embryogenesis harbors ubiquitous polygenic modifier
variation |
title_full | Wild worm embryogenesis harbors ubiquitous polygenic modifier
variation |
title_fullStr | Wild worm embryogenesis harbors ubiquitous polygenic modifier
variation |
title_full_unstemmed | Wild worm embryogenesis harbors ubiquitous polygenic modifier
variation |
title_short | Wild worm embryogenesis harbors ubiquitous polygenic modifier
variation |
title_sort | wild worm embryogenesis harbors ubiquitous polygenic modifier
variation |
topic | Genomics and Evolutionary Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4569889/ https://www.ncbi.nlm.nih.gov/pubmed/26297805 http://dx.doi.org/10.7554/eLife.09178 |
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