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Identification, Characterization, and Heritability of Murine Metastable Epialleles: Implications for Non-genetic Inheritance
Generally repressed by epigenetic mechanisms, retrotransposons represent around 40% of the murine genome. At the Agouti viable yellow (A(vy)) locus, an endogenous retrovirus (ERV) of the intracisternal A particle (IAP) class retrotransposed upstream of the agouti coat-color locus, providing an alter...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6242299/ https://www.ncbi.nlm.nih.gov/pubmed/30454646 http://dx.doi.org/10.1016/j.cell.2018.09.043 |
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author | Kazachenka, Anastasiya Bertozzi, Tessa M. Sjoberg-Herrera, Marcela K. Walker, Nic Gardner, Joseph Gunning, Richard Pahita, Elena Adams, Sarah Adams, David Ferguson-Smith, Anne C. |
author_facet | Kazachenka, Anastasiya Bertozzi, Tessa M. Sjoberg-Herrera, Marcela K. Walker, Nic Gardner, Joseph Gunning, Richard Pahita, Elena Adams, Sarah Adams, David Ferguson-Smith, Anne C. |
author_sort | Kazachenka, Anastasiya |
collection | PubMed |
description | Generally repressed by epigenetic mechanisms, retrotransposons represent around 40% of the murine genome. At the Agouti viable yellow (A(vy)) locus, an endogenous retrovirus (ERV) of the intracisternal A particle (IAP) class retrotransposed upstream of the agouti coat-color locus, providing an alternative promoter that is variably DNA methylated in genetically identical individuals. This results in variable expressivity of coat color that is inherited transgenerationally. Here, a systematic genome-wide screen identifies multiple C57BL/6J murine IAPs with A(vy) epigenetic properties. Each exhibits a stable methylation state within an individual but varies between individuals. Only in rare instances do they act as promoters controlling adjacent gene expression. Their methylation state is locus-specific within an individual, and their flanking regions are enriched for CTCF. Variably methylated IAPs are reprogrammed after fertilization and re-established as variable loci in the next generation, indicating reconstruction of metastable epigenetic states and challenging the generalizability of non-genetic inheritance at these regions. |
format | Online Article Text |
id | pubmed-6242299 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-62422992018-11-21 Identification, Characterization, and Heritability of Murine Metastable Epialleles: Implications for Non-genetic Inheritance Kazachenka, Anastasiya Bertozzi, Tessa M. Sjoberg-Herrera, Marcela K. Walker, Nic Gardner, Joseph Gunning, Richard Pahita, Elena Adams, Sarah Adams, David Ferguson-Smith, Anne C. Cell Article Generally repressed by epigenetic mechanisms, retrotransposons represent around 40% of the murine genome. At the Agouti viable yellow (A(vy)) locus, an endogenous retrovirus (ERV) of the intracisternal A particle (IAP) class retrotransposed upstream of the agouti coat-color locus, providing an alternative promoter that is variably DNA methylated in genetically identical individuals. This results in variable expressivity of coat color that is inherited transgenerationally. Here, a systematic genome-wide screen identifies multiple C57BL/6J murine IAPs with A(vy) epigenetic properties. Each exhibits a stable methylation state within an individual but varies between individuals. Only in rare instances do they act as promoters controlling adjacent gene expression. Their methylation state is locus-specific within an individual, and their flanking regions are enriched for CTCF. Variably methylated IAPs are reprogrammed after fertilization and re-established as variable loci in the next generation, indicating reconstruction of metastable epigenetic states and challenging the generalizability of non-genetic inheritance at these regions. Cell Press 2018-11-15 /pmc/articles/PMC6242299/ /pubmed/30454646 http://dx.doi.org/10.1016/j.cell.2018.09.043 Text en © 2018 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Kazachenka, Anastasiya Bertozzi, Tessa M. Sjoberg-Herrera, Marcela K. Walker, Nic Gardner, Joseph Gunning, Richard Pahita, Elena Adams, Sarah Adams, David Ferguson-Smith, Anne C. Identification, Characterization, and Heritability of Murine Metastable Epialleles: Implications for Non-genetic Inheritance |
title | Identification, Characterization, and Heritability of Murine Metastable Epialleles: Implications for Non-genetic Inheritance |
title_full | Identification, Characterization, and Heritability of Murine Metastable Epialleles: Implications for Non-genetic Inheritance |
title_fullStr | Identification, Characterization, and Heritability of Murine Metastable Epialleles: Implications for Non-genetic Inheritance |
title_full_unstemmed | Identification, Characterization, and Heritability of Murine Metastable Epialleles: Implications for Non-genetic Inheritance |
title_short | Identification, Characterization, and Heritability of Murine Metastable Epialleles: Implications for Non-genetic Inheritance |
title_sort | identification, characterization, and heritability of murine metastable epialleles: implications for non-genetic inheritance |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6242299/ https://www.ncbi.nlm.nih.gov/pubmed/30454646 http://dx.doi.org/10.1016/j.cell.2018.09.043 |
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