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A primer on the use of mouse models for identifying direct sex chromosome effects that cause sex differences in non-gonadal tissues
In animals with heteromorphic sex chromosomes, all sex differences originate from the sex chromosomes, which are the only factors that are consistently different in male and female zygotes. In mammals, the imbalance in Y gene expression, specifically the presence vs. absence of Sry, initiates the di...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5154145/ https://www.ncbi.nlm.nih.gov/pubmed/27999654 http://dx.doi.org/10.1186/s13293-016-0115-5 |
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author | Burgoyne, Paul S. Arnold, Arthur P. |
author_facet | Burgoyne, Paul S. Arnold, Arthur P. |
author_sort | Burgoyne, Paul S. |
collection | PubMed |
description | In animals with heteromorphic sex chromosomes, all sex differences originate from the sex chromosomes, which are the only factors that are consistently different in male and female zygotes. In mammals, the imbalance in Y gene expression, specifically the presence vs. absence of Sry, initiates the differentiation of testes in males, setting up lifelong sex differences in the level of gonadal hormones, which in turn cause many sex differences in the phenotype of non-gonadal tissues. The inherent imbalance in the expression of X and Y genes, or in the epigenetic impact of X and Y chromosomes, also has the potential to contribute directly to the sexual differentiation of non-gonadal cells. Here, we review the research strategies to identify the X and Y genes or chromosomal regions that cause direct, sexually differentiating effects on non-gonadal cells. Some mouse models are useful for separating the effects of sex chromosomes from those of gonadal hormones. Once direct “sex chromosome effects” are detected in these models, further studies are required to narrow down the list of candidate X and/or Y genes and then to identify the sexually differentiating genes themselves. Logical approaches to the search for these genes are reviewed here. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13293-016-0115-5) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5154145 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-51541452016-12-20 A primer on the use of mouse models for identifying direct sex chromosome effects that cause sex differences in non-gonadal tissues Burgoyne, Paul S. Arnold, Arthur P. Biol Sex Differ Review In animals with heteromorphic sex chromosomes, all sex differences originate from the sex chromosomes, which are the only factors that are consistently different in male and female zygotes. In mammals, the imbalance in Y gene expression, specifically the presence vs. absence of Sry, initiates the differentiation of testes in males, setting up lifelong sex differences in the level of gonadal hormones, which in turn cause many sex differences in the phenotype of non-gonadal tissues. The inherent imbalance in the expression of X and Y genes, or in the epigenetic impact of X and Y chromosomes, also has the potential to contribute directly to the sexual differentiation of non-gonadal cells. Here, we review the research strategies to identify the X and Y genes or chromosomal regions that cause direct, sexually differentiating effects on non-gonadal cells. Some mouse models are useful for separating the effects of sex chromosomes from those of gonadal hormones. Once direct “sex chromosome effects” are detected in these models, further studies are required to narrow down the list of candidate X and/or Y genes and then to identify the sexually differentiating genes themselves. Logical approaches to the search for these genes are reviewed here. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13293-016-0115-5) contains supplementary material, which is available to authorized users. BioMed Central 2016-12-13 /pmc/articles/PMC5154145/ /pubmed/27999654 http://dx.doi.org/10.1186/s13293-016-0115-5 Text en © The Author(s). 2016 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 | Review Burgoyne, Paul S. Arnold, Arthur P. A primer on the use of mouse models for identifying direct sex chromosome effects that cause sex differences in non-gonadal tissues |
title | A primer on the use of mouse models for identifying direct sex chromosome effects that cause sex differences in non-gonadal tissues |
title_full | A primer on the use of mouse models for identifying direct sex chromosome effects that cause sex differences in non-gonadal tissues |
title_fullStr | A primer on the use of mouse models for identifying direct sex chromosome effects that cause sex differences in non-gonadal tissues |
title_full_unstemmed | A primer on the use of mouse models for identifying direct sex chromosome effects that cause sex differences in non-gonadal tissues |
title_short | A primer on the use of mouse models for identifying direct sex chromosome effects that cause sex differences in non-gonadal tissues |
title_sort | primer on the use of mouse models for identifying direct sex chromosome effects that cause sex differences in non-gonadal tissues |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5154145/ https://www.ncbi.nlm.nih.gov/pubmed/27999654 http://dx.doi.org/10.1186/s13293-016-0115-5 |
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