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Autosomal monoallelic expression in the mouse
BACKGROUND: Random monoallelic expression defines an unusual class of genes displaying random choice for expression between the maternal and paternal alleles. Once established, the allele-specific expression pattern is stably maintained and mitotically inherited. Examples of random monoallelic genes...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3334567/ https://www.ncbi.nlm.nih.gov/pubmed/22348269 http://dx.doi.org/10.1186/gb-2012-13-2-r10 |
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author | Zwemer, Lillian M Zak, Alexander Thompson, Benjamin R Kirby, Andrew Daly, Mark J Chess, Andrew Gimelbrant, Alexander A |
author_facet | Zwemer, Lillian M Zak, Alexander Thompson, Benjamin R Kirby, Andrew Daly, Mark J Chess, Andrew Gimelbrant, Alexander A |
author_sort | Zwemer, Lillian M |
collection | PubMed |
description | BACKGROUND: Random monoallelic expression defines an unusual class of genes displaying random choice for expression between the maternal and paternal alleles. Once established, the allele-specific expression pattern is stably maintained and mitotically inherited. Examples of random monoallelic genes include those found on the X-chromosome and a subset of autosomal genes, which have been most extensively studied in humans. Here, we report a genome-wide analysis of random monoallelic expression in the mouse. We used high density mouse genome polymorphism mapping arrays to assess allele-specific expression in clonal cell lines derived from heterozygous mouse strains. RESULTS: Over 1,300 autosomal genes were assessed for allele-specific expression, and greater than 10% of them showed random monoallelic expression. When comparing mouse and human, the number of autosomal orthologs demonstrating random monoallelic expression in both organisms was greater than would be expected by chance. Random monoallelic expression on the mouse autosomes is broadly similar to that in human cells: it is widespread throughout the genome, lacks chromosome-wide coordination, and varies between cell types. However, for some mouse genes, there appears to be skewing, in some ways resembling skewed X-inactivation, wherein one allele is more frequently active. CONCLUSIONS: These data suggest that autosomal random monoallelic expression was present at least as far back as the last common ancestor of rodents and primates. Random monoallelic expression can lead to phenotypic variation beyond the phenotypic variation dictated by genotypic variation. Thus, it is important to take into account random monoallelic expression when examining genotype-phenotype correlation. |
format | Online Article Text |
id | pubmed-3334567 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-33345672012-04-25 Autosomal monoallelic expression in the mouse Zwemer, Lillian M Zak, Alexander Thompson, Benjamin R Kirby, Andrew Daly, Mark J Chess, Andrew Gimelbrant, Alexander A Genome Biol Research BACKGROUND: Random monoallelic expression defines an unusual class of genes displaying random choice for expression between the maternal and paternal alleles. Once established, the allele-specific expression pattern is stably maintained and mitotically inherited. Examples of random monoallelic genes include those found on the X-chromosome and a subset of autosomal genes, which have been most extensively studied in humans. Here, we report a genome-wide analysis of random monoallelic expression in the mouse. We used high density mouse genome polymorphism mapping arrays to assess allele-specific expression in clonal cell lines derived from heterozygous mouse strains. RESULTS: Over 1,300 autosomal genes were assessed for allele-specific expression, and greater than 10% of them showed random monoallelic expression. When comparing mouse and human, the number of autosomal orthologs demonstrating random monoallelic expression in both organisms was greater than would be expected by chance. Random monoallelic expression on the mouse autosomes is broadly similar to that in human cells: it is widespread throughout the genome, lacks chromosome-wide coordination, and varies between cell types. However, for some mouse genes, there appears to be skewing, in some ways resembling skewed X-inactivation, wherein one allele is more frequently active. CONCLUSIONS: These data suggest that autosomal random monoallelic expression was present at least as far back as the last common ancestor of rodents and primates. Random monoallelic expression can lead to phenotypic variation beyond the phenotypic variation dictated by genotypic variation. Thus, it is important to take into account random monoallelic expression when examining genotype-phenotype correlation. BioMed Central 2012 2012-02-20 /pmc/articles/PMC3334567/ /pubmed/22348269 http://dx.doi.org/10.1186/gb-2012-13-2-r10 Text en Copyright ©2012 Zwemer et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Zwemer, Lillian M Zak, Alexander Thompson, Benjamin R Kirby, Andrew Daly, Mark J Chess, Andrew Gimelbrant, Alexander A Autosomal monoallelic expression in the mouse |
title | Autosomal monoallelic expression in the mouse |
title_full | Autosomal monoallelic expression in the mouse |
title_fullStr | Autosomal monoallelic expression in the mouse |
title_full_unstemmed | Autosomal monoallelic expression in the mouse |
title_short | Autosomal monoallelic expression in the mouse |
title_sort | autosomal monoallelic expression in the mouse |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3334567/ https://www.ncbi.nlm.nih.gov/pubmed/22348269 http://dx.doi.org/10.1186/gb-2012-13-2-r10 |
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