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Abiotic and past climatic conditions drive protein abundance variation among natural populations of the caddisfly Crunoecia irrorata
Deducing impacts of environmental change on species and the populations they form in nature is an important goal in contemporary ecology. Achieving this goal is hampered by our limited understanding of the influence of naturally occurring environmental variation on the molecular systems of ecologica...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7512004/ https://www.ncbi.nlm.nih.gov/pubmed/32968134 http://dx.doi.org/10.1038/s41598-020-72569-4 |
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author | Ebner, Joshua Niklas Ritz, Danilo von Fumetti, Stefanie |
author_facet | Ebner, Joshua Niklas Ritz, Danilo von Fumetti, Stefanie |
author_sort | Ebner, Joshua Niklas |
collection | PubMed |
description | Deducing impacts of environmental change on species and the populations they form in nature is an important goal in contemporary ecology. Achieving this goal is hampered by our limited understanding of the influence of naturally occurring environmental variation on the molecular systems of ecologically relevant species, as the pathways underlying fitness-affecting plastic responses have primarily been studied in model organisms and under controlled laboratory conditions. Here, to test the hypothesis that proteome variation systematically relates to variation in abiotic conditions, we establish such relationships by profiling the proteomes of 24 natural populations of the spring-dwelling caddisfly Crunoecia irrorata. We identified protein networks whose abundances correlated with environmental (abiotic) gradients such as in situ pH, oxygen- and nitrate concentrations but also climatic data such as past thermal minima and temperature seasonality. Our analyses suggest that variations in abiotic conditions induce discrete proteome responses such as the differential abundance of proteins associated with cytoskeletal function, heat-shock proteins and proteins related to post-translational modification. Identifying these drivers of proteome divergence characterizes molecular “noise”, and positions it as a background against which molecular signatures of species’ adaptive responses to stressful conditions can be identified. |
format | Online Article Text |
id | pubmed-7512004 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-75120042020-09-29 Abiotic and past climatic conditions drive protein abundance variation among natural populations of the caddisfly Crunoecia irrorata Ebner, Joshua Niklas Ritz, Danilo von Fumetti, Stefanie Sci Rep Article Deducing impacts of environmental change on species and the populations they form in nature is an important goal in contemporary ecology. Achieving this goal is hampered by our limited understanding of the influence of naturally occurring environmental variation on the molecular systems of ecologically relevant species, as the pathways underlying fitness-affecting plastic responses have primarily been studied in model organisms and under controlled laboratory conditions. Here, to test the hypothesis that proteome variation systematically relates to variation in abiotic conditions, we establish such relationships by profiling the proteomes of 24 natural populations of the spring-dwelling caddisfly Crunoecia irrorata. We identified protein networks whose abundances correlated with environmental (abiotic) gradients such as in situ pH, oxygen- and nitrate concentrations but also climatic data such as past thermal minima and temperature seasonality. Our analyses suggest that variations in abiotic conditions induce discrete proteome responses such as the differential abundance of proteins associated with cytoskeletal function, heat-shock proteins and proteins related to post-translational modification. Identifying these drivers of proteome divergence characterizes molecular “noise”, and positions it as a background against which molecular signatures of species’ adaptive responses to stressful conditions can be identified. Nature Publishing Group UK 2020-09-23 /pmc/articles/PMC7512004/ /pubmed/32968134 http://dx.doi.org/10.1038/s41598-020-72569-4 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Ebner, Joshua Niklas Ritz, Danilo von Fumetti, Stefanie Abiotic and past climatic conditions drive protein abundance variation among natural populations of the caddisfly Crunoecia irrorata |
title | Abiotic and past climatic conditions drive protein abundance variation among natural populations of the caddisfly Crunoecia irrorata |
title_full | Abiotic and past climatic conditions drive protein abundance variation among natural populations of the caddisfly Crunoecia irrorata |
title_fullStr | Abiotic and past climatic conditions drive protein abundance variation among natural populations of the caddisfly Crunoecia irrorata |
title_full_unstemmed | Abiotic and past climatic conditions drive protein abundance variation among natural populations of the caddisfly Crunoecia irrorata |
title_short | Abiotic and past climatic conditions drive protein abundance variation among natural populations of the caddisfly Crunoecia irrorata |
title_sort | abiotic and past climatic conditions drive protein abundance variation among natural populations of the caddisfly crunoecia irrorata |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7512004/ https://www.ncbi.nlm.nih.gov/pubmed/32968134 http://dx.doi.org/10.1038/s41598-020-72569-4 |
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