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Sex differences in early transcriptomic responses to oxidative stress in the copepod Tigriopus californicus

BACKGROUND: Patterns of gene expression can be dramatically different between males and females of the same species, in part due to genes on sex chromosomes. Here we test for sex differences in early transcriptomic response to oxidative stress in a species which lacks heteromorphic sex chromosomes,...

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Autores principales: Li, Ning, Flanagan, Ben A., Partridge, MacKenzie, Huang, Elaine J., Edmands, Suzanne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7607713/
https://www.ncbi.nlm.nih.gov/pubmed/33143643
http://dx.doi.org/10.1186/s12864-020-07179-5
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author Li, Ning
Flanagan, Ben A.
Partridge, MacKenzie
Huang, Elaine J.
Edmands, Suzanne
author_facet Li, Ning
Flanagan, Ben A.
Partridge, MacKenzie
Huang, Elaine J.
Edmands, Suzanne
author_sort Li, Ning
collection PubMed
description BACKGROUND: Patterns of gene expression can be dramatically different between males and females of the same species, in part due to genes on sex chromosomes. Here we test for sex differences in early transcriptomic response to oxidative stress in a species which lacks heteromorphic sex chromosomes, the copepod Tigriopus californicus. RESULTS: Male and female individuals were separately exposed to control conditions and pro-oxidant conditions (hydrogen peroxide and paraquat) for periods of 3 hours and 6 hours. Variance partitioning showed the greatest expression variance among individuals, highlighting the important information that can be obscured by the common practice of pooling individuals. Gene expression variance between sexes was greater than that among treatments, showing the profound effect of sex even when males and females share the same genome. Males exhibited a larger response to both pro-oxidants, differentially expressing more than four times as many genes, including up-regulation of more antioxidant genes, heat shock proteins and protease genes. While females differentially expressed fewer genes, the magnitudes of fold change were generally greater, indicating a more targeted response. Although females shared a smaller fraction of differentially expressed genes between stressors and time points, expression patterns of antioxidant and protease genes were more similar between stressors and more GO terms were shared between time points. CONCLUSIONS: Early transcriptomic responses to the pro-oxidants H(2)O(2) and paraquat in copepods revealed substantial variation among individuals and between sexes. The finding of such profound sex differences in oxidative stress response, even in the absence of sex chromosomes, highlights the importance of studying both sexes and the potential for developing sex-specific strategies to promote optimal health and aging in humans. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-020-07179-5.
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spelling pubmed-76077132020-11-03 Sex differences in early transcriptomic responses to oxidative stress in the copepod Tigriopus californicus Li, Ning Flanagan, Ben A. Partridge, MacKenzie Huang, Elaine J. Edmands, Suzanne BMC Genomics Research Article BACKGROUND: Patterns of gene expression can be dramatically different between males and females of the same species, in part due to genes on sex chromosomes. Here we test for sex differences in early transcriptomic response to oxidative stress in a species which lacks heteromorphic sex chromosomes, the copepod Tigriopus californicus. RESULTS: Male and female individuals were separately exposed to control conditions and pro-oxidant conditions (hydrogen peroxide and paraquat) for periods of 3 hours and 6 hours. Variance partitioning showed the greatest expression variance among individuals, highlighting the important information that can be obscured by the common practice of pooling individuals. Gene expression variance between sexes was greater than that among treatments, showing the profound effect of sex even when males and females share the same genome. Males exhibited a larger response to both pro-oxidants, differentially expressing more than four times as many genes, including up-regulation of more antioxidant genes, heat shock proteins and protease genes. While females differentially expressed fewer genes, the magnitudes of fold change were generally greater, indicating a more targeted response. Although females shared a smaller fraction of differentially expressed genes between stressors and time points, expression patterns of antioxidant and protease genes were more similar between stressors and more GO terms were shared between time points. CONCLUSIONS: Early transcriptomic responses to the pro-oxidants H(2)O(2) and paraquat in copepods revealed substantial variation among individuals and between sexes. The finding of such profound sex differences in oxidative stress response, even in the absence of sex chromosomes, highlights the importance of studying both sexes and the potential for developing sex-specific strategies to promote optimal health and aging in humans. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-020-07179-5. BioMed Central 2020-11-03 /pmc/articles/PMC7607713/ /pubmed/33143643 http://dx.doi.org/10.1186/s12864-020-07179-5 Text en © The Author(s) 2020 Open AccessThis 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/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Li, Ning
Flanagan, Ben A.
Partridge, MacKenzie
Huang, Elaine J.
Edmands, Suzanne
Sex differences in early transcriptomic responses to oxidative stress in the copepod Tigriopus californicus
title Sex differences in early transcriptomic responses to oxidative stress in the copepod Tigriopus californicus
title_full Sex differences in early transcriptomic responses to oxidative stress in the copepod Tigriopus californicus
title_fullStr Sex differences in early transcriptomic responses to oxidative stress in the copepod Tigriopus californicus
title_full_unstemmed Sex differences in early transcriptomic responses to oxidative stress in the copepod Tigriopus californicus
title_short Sex differences in early transcriptomic responses to oxidative stress in the copepod Tigriopus californicus
title_sort sex differences in early transcriptomic responses to oxidative stress in the copepod tigriopus californicus
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7607713/
https://www.ncbi.nlm.nih.gov/pubmed/33143643
http://dx.doi.org/10.1186/s12864-020-07179-5
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