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Diet, gonadal sex, and sex chromosome complement influence white adipose tissue miRNA expression

BACKGROUND: MicroRNAs (miRNAs) are small non-coding RNA molecules that regulate gene expression by targeting specific mRNA species for degradation or interfering with translation. Specific miRNAs are key regulators of adipogenesis, and are expressed at different levels in adipose tissue from lean an...

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Autores principales: Link, Jenny C., Hasin-Brumshtein, Yehudit, Cantor, Rita M., Chen, Xuqi, Arnold, Arthur P., Lusis, Aldons J., Reue, Karen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5240420/
https://www.ncbi.nlm.nih.gov/pubmed/28095800
http://dx.doi.org/10.1186/s12864-017-3484-1
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author Link, Jenny C.
Hasin-Brumshtein, Yehudit
Cantor, Rita M.
Chen, Xuqi
Arnold, Arthur P.
Lusis, Aldons J.
Reue, Karen
author_facet Link, Jenny C.
Hasin-Brumshtein, Yehudit
Cantor, Rita M.
Chen, Xuqi
Arnold, Arthur P.
Lusis, Aldons J.
Reue, Karen
author_sort Link, Jenny C.
collection PubMed
description BACKGROUND: MicroRNAs (miRNAs) are small non-coding RNA molecules that regulate gene expression by targeting specific mRNA species for degradation or interfering with translation. Specific miRNAs are key regulators of adipogenesis, and are expressed at different levels in adipose tissue from lean and obese mice. The degree of lipid accumulation and distribution of white adipose tissue differs between males and females, and it is unknown whether sex differences in adipose tissue-specific miRNA expression may contribute to this dimorphism. Typically, sex differences are attributed to hormones secreted from ovaries or testes. However, the sex chromosome complement (XX versus XY) is also a determinant of sex differences and may regulate miRNA expression in adipocytes. RESULTS: To identify sex differences in adipose tissue miRNA expression and to understand the underlying mechanisms, we performed high-throughput miRNA sequencing in gonadal fat depots of the Four Core Genotypes mouse model. This model, which consists of XX female, XX male, XY female, and XY male mice, allowed us to assess independent effects of gonadal type (male vs. female) and sex chromosome complement (XX vs. XY) on miRNA expression profiles. We have also assessed the effects of a high fat diet on sex differences in adipose tissue miRNA profiles. We identified a male–female effect on the overall miRNA expression profile in mice fed a chow diet, with a bias toward higher expression in male compared to female gonadal adipose tissue. This sex bias disappeared after gonadectomy, suggesting that circulating levels of gonadal secretions modulate the miRNA expression profile. After 16 weeks of high fat diet, the miRNA expression distribution was shifted toward higher expression in XY vs. XX adipose tissue. Principal component analysis revealed that high fat diet has a substantial effect on miRNA profile variance, while gonadal secretions and sex chromosome complement each have milder effects. CONCLUSIONS: Our results demonstrate that the overall miRNA expression profile in adipose tissue is influenced by gonadal hormones and the sex chromosome complement, and that expression profiles change in response to gonadectomy and high fat diet. Differential miRNA expression profiles may contribute to sex differences in adipose tissue gene expression, adipose tissue development, and diet-induced obesity. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-017-3484-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-52404202017-01-23 Diet, gonadal sex, and sex chromosome complement influence white adipose tissue miRNA expression Link, Jenny C. Hasin-Brumshtein, Yehudit Cantor, Rita M. Chen, Xuqi Arnold, Arthur P. Lusis, Aldons J. Reue, Karen BMC Genomics Research Article BACKGROUND: MicroRNAs (miRNAs) are small non-coding RNA molecules that regulate gene expression by targeting specific mRNA species for degradation or interfering with translation. Specific miRNAs are key regulators of adipogenesis, and are expressed at different levels in adipose tissue from lean and obese mice. The degree of lipid accumulation and distribution of white adipose tissue differs between males and females, and it is unknown whether sex differences in adipose tissue-specific miRNA expression may contribute to this dimorphism. Typically, sex differences are attributed to hormones secreted from ovaries or testes. However, the sex chromosome complement (XX versus XY) is also a determinant of sex differences and may regulate miRNA expression in adipocytes. RESULTS: To identify sex differences in adipose tissue miRNA expression and to understand the underlying mechanisms, we performed high-throughput miRNA sequencing in gonadal fat depots of the Four Core Genotypes mouse model. This model, which consists of XX female, XX male, XY female, and XY male mice, allowed us to assess independent effects of gonadal type (male vs. female) and sex chromosome complement (XX vs. XY) on miRNA expression profiles. We have also assessed the effects of a high fat diet on sex differences in adipose tissue miRNA profiles. We identified a male–female effect on the overall miRNA expression profile in mice fed a chow diet, with a bias toward higher expression in male compared to female gonadal adipose tissue. This sex bias disappeared after gonadectomy, suggesting that circulating levels of gonadal secretions modulate the miRNA expression profile. After 16 weeks of high fat diet, the miRNA expression distribution was shifted toward higher expression in XY vs. XX adipose tissue. Principal component analysis revealed that high fat diet has a substantial effect on miRNA profile variance, while gonadal secretions and sex chromosome complement each have milder effects. CONCLUSIONS: Our results demonstrate that the overall miRNA expression profile in adipose tissue is influenced by gonadal hormones and the sex chromosome complement, and that expression profiles change in response to gonadectomy and high fat diet. Differential miRNA expression profiles may contribute to sex differences in adipose tissue gene expression, adipose tissue development, and diet-induced obesity. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-017-3484-1) contains supplementary material, which is available to authorized users. BioMed Central 2017-01-17 /pmc/articles/PMC5240420/ /pubmed/28095800 http://dx.doi.org/10.1186/s12864-017-3484-1 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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.
spellingShingle Research Article
Link, Jenny C.
Hasin-Brumshtein, Yehudit
Cantor, Rita M.
Chen, Xuqi
Arnold, Arthur P.
Lusis, Aldons J.
Reue, Karen
Diet, gonadal sex, and sex chromosome complement influence white adipose tissue miRNA expression
title Diet, gonadal sex, and sex chromosome complement influence white adipose tissue miRNA expression
title_full Diet, gonadal sex, and sex chromosome complement influence white adipose tissue miRNA expression
title_fullStr Diet, gonadal sex, and sex chromosome complement influence white adipose tissue miRNA expression
title_full_unstemmed Diet, gonadal sex, and sex chromosome complement influence white adipose tissue miRNA expression
title_short Diet, gonadal sex, and sex chromosome complement influence white adipose tissue miRNA expression
title_sort diet, gonadal sex, and sex chromosome complement influence white adipose tissue mirna expression
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5240420/
https://www.ncbi.nlm.nih.gov/pubmed/28095800
http://dx.doi.org/10.1186/s12864-017-3484-1
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