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Epigenetic transgenerational inheritance of somatic transcriptomes and epigenetic control regions
BACKGROUND: Environmentally induced epigenetic transgenerational inheritance of adult onset disease involves a variety of phenotypic changes, suggesting a general alteration in genome activity. RESULTS: Investigation of different tissue transcriptomes in male and female F3 generation vinclozolin ver...
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/PMC3491419/ https://www.ncbi.nlm.nih.gov/pubmed/23034163 http://dx.doi.org/10.1186/gb-2012-13-10-r91 |
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author | Skinner, Michael K Mohan, Manikkam Haque, Md M Zhang, Bin Savenkova, Marina I |
author_facet | Skinner, Michael K Mohan, Manikkam Haque, Md M Zhang, Bin Savenkova, Marina I |
author_sort | Skinner, Michael K |
collection | PubMed |
description | BACKGROUND: Environmentally induced epigenetic transgenerational inheritance of adult onset disease involves a variety of phenotypic changes, suggesting a general alteration in genome activity. RESULTS: Investigation of different tissue transcriptomes in male and female F3 generation vinclozolin versus control lineage rats demonstrated all tissues examined had transgenerational transcriptomes. The microarrays from 11 different tissues were compared with a gene bionetwork analysis. Although each tissue transgenerational transcriptome was unique, common cellular pathways and processes were identified between the tissues. A cluster analysis identified gene modules with coordinated gene expression and each had unique gene networks regulating tissue-specific gene expression and function. A large number of statistically significant over-represented clusters of genes were identified in the genome for both males and females. These gene clusters ranged from 2-5 megabases in size, and a number of them corresponded to the epimutations previously identified in sperm that transmit the epigenetic transgenerational inheritance of disease phenotypes. CONCLUSIONS: Combined observations demonstrate that all tissues derived from the epigenetically altered germ line develop transgenerational transcriptomes unique to the tissue, but common epigenetic control regions in the genome may coordinately regulate these tissue-specific transcriptomes. This systems biology approach provides insight into the molecular mechanisms involved in the epigenetic transgenerational inheritance of a variety of adult onset disease phenotypes. |
format | Online Article Text |
id | pubmed-3491419 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-34914192012-11-08 Epigenetic transgenerational inheritance of somatic transcriptomes and epigenetic control regions Skinner, Michael K Mohan, Manikkam Haque, Md M Zhang, Bin Savenkova, Marina I Genome Biol Research BACKGROUND: Environmentally induced epigenetic transgenerational inheritance of adult onset disease involves a variety of phenotypic changes, suggesting a general alteration in genome activity. RESULTS: Investigation of different tissue transcriptomes in male and female F3 generation vinclozolin versus control lineage rats demonstrated all tissues examined had transgenerational transcriptomes. The microarrays from 11 different tissues were compared with a gene bionetwork analysis. Although each tissue transgenerational transcriptome was unique, common cellular pathways and processes were identified between the tissues. A cluster analysis identified gene modules with coordinated gene expression and each had unique gene networks regulating tissue-specific gene expression and function. A large number of statistically significant over-represented clusters of genes were identified in the genome for both males and females. These gene clusters ranged from 2-5 megabases in size, and a number of them corresponded to the epimutations previously identified in sperm that transmit the epigenetic transgenerational inheritance of disease phenotypes. CONCLUSIONS: Combined observations demonstrate that all tissues derived from the epigenetically altered germ line develop transgenerational transcriptomes unique to the tissue, but common epigenetic control regions in the genome may coordinately regulate these tissue-specific transcriptomes. This systems biology approach provides insight into the molecular mechanisms involved in the epigenetic transgenerational inheritance of a variety of adult onset disease phenotypes. BioMed Central 2012 2012-10-03 /pmc/articles/PMC3491419/ /pubmed/23034163 http://dx.doi.org/10.1186/gb-2012-13-10-r91 Text en Copyright ©2012 Skinner 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 Skinner, Michael K Mohan, Manikkam Haque, Md M Zhang, Bin Savenkova, Marina I Epigenetic transgenerational inheritance of somatic transcriptomes and epigenetic control regions |
title | Epigenetic transgenerational inheritance of somatic transcriptomes and epigenetic control
regions |
title_full | Epigenetic transgenerational inheritance of somatic transcriptomes and epigenetic control
regions |
title_fullStr | Epigenetic transgenerational inheritance of somatic transcriptomes and epigenetic control
regions |
title_full_unstemmed | Epigenetic transgenerational inheritance of somatic transcriptomes and epigenetic control
regions |
title_short | Epigenetic transgenerational inheritance of somatic transcriptomes and epigenetic control
regions |
title_sort | epigenetic transgenerational inheritance of somatic transcriptomes and epigenetic control
regions |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3491419/ https://www.ncbi.nlm.nih.gov/pubmed/23034163 http://dx.doi.org/10.1186/gb-2012-13-10-r91 |
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