Cargando…

Ontogenetic Change in Male Expression of Testosterone-Responsive Genes Contributes to the Emergence of Sex-Biased Gene Expression in Anolis sagrei

Sex differences in gene expression tend to increase with age across a variety of species, often coincident with the development of sexual dimorphism and maturational changes in hormone levels. However, because most transcriptome-wide characterizations of sexual divergence are framed as comparisons o...

Descripción completa

Detalles Bibliográficos
Autores principales: Hale, Matthew D., Robinson, Christopher D., Cox, Christian L., Cox, Robert M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9203151/
https://www.ncbi.nlm.nih.gov/pubmed/35721538
http://dx.doi.org/10.3389/fphys.2022.886973
_version_ 1784728667102904320
author Hale, Matthew D.
Robinson, Christopher D.
Cox, Christian L.
Cox, Robert M.
author_facet Hale, Matthew D.
Robinson, Christopher D.
Cox, Christian L.
Cox, Robert M.
author_sort Hale, Matthew D.
collection PubMed
description Sex differences in gene expression tend to increase with age across a variety of species, often coincident with the development of sexual dimorphism and maturational changes in hormone levels. However, because most transcriptome-wide characterizations of sexual divergence are framed as comparisons of sex-biased gene expression across ages, it can be difficult to determine the extent to which age-biased gene expression within each sex contributes to the emergence of sex-biased gene expression. Using RNAseq in the liver of the sexually dimorphic brown anole lizard (Anolis sagrei), we found that a pronounced increase in sex-biased gene expression with age was associated with a much greater degree of age-biased gene expression in males than in females. This pattern suggests that developmental changes in males, such as maturational increases in circulating testosterone, contribute disproportionately to the ontogenetic emergence of sex-biased gene expression. To test this hypothesis, we used four different experimental contrasts to independently characterize sets of genes whose expression differed as a function of castration and/or treatment with exogenous testosterone. We found that genes that were significantly male-biased in expression or upregulated as males matured tended to be upregulated by testosterone, whereas genes that were female-biased or downregulated as males matured tended to be downregulated by testosterone. Moreover, the first two principal components describing multivariate gene expression indicated that exogenous testosterone reversed many of the feminizing effects of castration on the liver transcriptome of maturing males. Collectively, our results suggest that developmental changes that occur in males contribute disproportionately to the emergence of sex-biased gene expression in the Anolis liver, and that many of these changes are orchestrated by androgens such as testosterone.
format Online
Article
Text
id pubmed-9203151
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-92031512022-06-17 Ontogenetic Change in Male Expression of Testosterone-Responsive Genes Contributes to the Emergence of Sex-Biased Gene Expression in Anolis sagrei Hale, Matthew D. Robinson, Christopher D. Cox, Christian L. Cox, Robert M. Front Physiol Physiology Sex differences in gene expression tend to increase with age across a variety of species, often coincident with the development of sexual dimorphism and maturational changes in hormone levels. However, because most transcriptome-wide characterizations of sexual divergence are framed as comparisons of sex-biased gene expression across ages, it can be difficult to determine the extent to which age-biased gene expression within each sex contributes to the emergence of sex-biased gene expression. Using RNAseq in the liver of the sexually dimorphic brown anole lizard (Anolis sagrei), we found that a pronounced increase in sex-biased gene expression with age was associated with a much greater degree of age-biased gene expression in males than in females. This pattern suggests that developmental changes in males, such as maturational increases in circulating testosterone, contribute disproportionately to the ontogenetic emergence of sex-biased gene expression. To test this hypothesis, we used four different experimental contrasts to independently characterize sets of genes whose expression differed as a function of castration and/or treatment with exogenous testosterone. We found that genes that were significantly male-biased in expression or upregulated as males matured tended to be upregulated by testosterone, whereas genes that were female-biased or downregulated as males matured tended to be downregulated by testosterone. Moreover, the first two principal components describing multivariate gene expression indicated that exogenous testosterone reversed many of the feminizing effects of castration on the liver transcriptome of maturing males. Collectively, our results suggest that developmental changes that occur in males contribute disproportionately to the emergence of sex-biased gene expression in the Anolis liver, and that many of these changes are orchestrated by androgens such as testosterone. Frontiers Media S.A. 2022-06-02 /pmc/articles/PMC9203151/ /pubmed/35721538 http://dx.doi.org/10.3389/fphys.2022.886973 Text en Copyright © 2022 Hale, Robinson, Cox and Cox. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Hale, Matthew D.
Robinson, Christopher D.
Cox, Christian L.
Cox, Robert M.
Ontogenetic Change in Male Expression of Testosterone-Responsive Genes Contributes to the Emergence of Sex-Biased Gene Expression in Anolis sagrei
title Ontogenetic Change in Male Expression of Testosterone-Responsive Genes Contributes to the Emergence of Sex-Biased Gene Expression in Anolis sagrei
title_full Ontogenetic Change in Male Expression of Testosterone-Responsive Genes Contributes to the Emergence of Sex-Biased Gene Expression in Anolis sagrei
title_fullStr Ontogenetic Change in Male Expression of Testosterone-Responsive Genes Contributes to the Emergence of Sex-Biased Gene Expression in Anolis sagrei
title_full_unstemmed Ontogenetic Change in Male Expression of Testosterone-Responsive Genes Contributes to the Emergence of Sex-Biased Gene Expression in Anolis sagrei
title_short Ontogenetic Change in Male Expression of Testosterone-Responsive Genes Contributes to the Emergence of Sex-Biased Gene Expression in Anolis sagrei
title_sort ontogenetic change in male expression of testosterone-responsive genes contributes to the emergence of sex-biased gene expression in anolis sagrei
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9203151/
https://www.ncbi.nlm.nih.gov/pubmed/35721538
http://dx.doi.org/10.3389/fphys.2022.886973
work_keys_str_mv AT halematthewd ontogeneticchangeinmaleexpressionoftestosteroneresponsivegenescontributestotheemergenceofsexbiasedgeneexpressioninanolissagrei
AT robinsonchristopherd ontogeneticchangeinmaleexpressionoftestosteroneresponsivegenescontributestotheemergenceofsexbiasedgeneexpressioninanolissagrei
AT coxchristianl ontogeneticchangeinmaleexpressionoftestosteroneresponsivegenescontributestotheemergenceofsexbiasedgeneexpressioninanolissagrei
AT coxrobertm ontogeneticchangeinmaleexpressionoftestosteroneresponsivegenescontributestotheemergenceofsexbiasedgeneexpressioninanolissagrei