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A Bayesian Model for the Analysis of Transgenerational Epigenetic Variation
Epigenetics has become one of the major areas of biological research. However, the degree of phenotypic variability that is explained by epigenetic processes still remains unclear. From a quantitative genetics perspective, the estimation of variance components is achieved by means of the information...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Genetics Society of America
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4390564/ https://www.ncbi.nlm.nih.gov/pubmed/25617408 http://dx.doi.org/10.1534/g3.115.016725 |
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author | Varona, Luis Munilla, Sebastián Mouresan, Elena Flavia González-Rodríguez, Aldemar Moreno, Carlos Altarriba, Juan |
author_facet | Varona, Luis Munilla, Sebastián Mouresan, Elena Flavia González-Rodríguez, Aldemar Moreno, Carlos Altarriba, Juan |
author_sort | Varona, Luis |
collection | PubMed |
description | Epigenetics has become one of the major areas of biological research. However, the degree of phenotypic variability that is explained by epigenetic processes still remains unclear. From a quantitative genetics perspective, the estimation of variance components is achieved by means of the information provided by the resemblance between relatives. In a previous study, this resemblance was described as a function of the epigenetic variance component and a reset coefficient that indicates the rate of dissipation of epigenetic marks across generations. Given these assumptions, we propose a Bayesian mixed model methodology that allows the estimation of epigenetic variance from a genealogical and phenotypic database. The methodology is based on the development of a T matrix of epigenetic relationships that depends on the reset coefficient. In addition, we present a simple procedure for the calculation of the inverse of this matrix (T(−1)) and a Gibbs sampler algorithm that obtains posterior estimates of all the unknowns in the model. The new procedure was used with two simulated data sets and with a beef cattle database. In the simulated populations, the results of the analysis provided marginal posterior distributions that included the population parameters in the regions of highest posterior density. In the case of the beef cattle dataset, the posterior estimate of transgenerational epigenetic variability was very low and a model comparison test indicated that a model that did not included it was the most plausible. |
format | Online Article Text |
id | pubmed-4390564 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Genetics Society of America |
record_format | MEDLINE/PubMed |
spelling | pubmed-43905642015-04-10 A Bayesian Model for the Analysis of Transgenerational Epigenetic Variation Varona, Luis Munilla, Sebastián Mouresan, Elena Flavia González-Rodríguez, Aldemar Moreno, Carlos Altarriba, Juan G3 (Bethesda) Investigations Epigenetics has become one of the major areas of biological research. However, the degree of phenotypic variability that is explained by epigenetic processes still remains unclear. From a quantitative genetics perspective, the estimation of variance components is achieved by means of the information provided by the resemblance between relatives. In a previous study, this resemblance was described as a function of the epigenetic variance component and a reset coefficient that indicates the rate of dissipation of epigenetic marks across generations. Given these assumptions, we propose a Bayesian mixed model methodology that allows the estimation of epigenetic variance from a genealogical and phenotypic database. The methodology is based on the development of a T matrix of epigenetic relationships that depends on the reset coefficient. In addition, we present a simple procedure for the calculation of the inverse of this matrix (T(−1)) and a Gibbs sampler algorithm that obtains posterior estimates of all the unknowns in the model. The new procedure was used with two simulated data sets and with a beef cattle database. In the simulated populations, the results of the analysis provided marginal posterior distributions that included the population parameters in the regions of highest posterior density. In the case of the beef cattle dataset, the posterior estimate of transgenerational epigenetic variability was very low and a model comparison test indicated that a model that did not included it was the most plausible. Genetics Society of America 2015-01-23 /pmc/articles/PMC4390564/ /pubmed/25617408 http://dx.doi.org/10.1534/g3.115.016725 Text en Copyright © 2015 Varona et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Unported License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Investigations Varona, Luis Munilla, Sebastián Mouresan, Elena Flavia González-Rodríguez, Aldemar Moreno, Carlos Altarriba, Juan A Bayesian Model for the Analysis of Transgenerational Epigenetic Variation |
title | A Bayesian Model for the Analysis of Transgenerational Epigenetic Variation |
title_full | A Bayesian Model for the Analysis of Transgenerational Epigenetic Variation |
title_fullStr | A Bayesian Model for the Analysis of Transgenerational Epigenetic Variation |
title_full_unstemmed | A Bayesian Model for the Analysis of Transgenerational Epigenetic Variation |
title_short | A Bayesian Model for the Analysis of Transgenerational Epigenetic Variation |
title_sort | bayesian model for the analysis of transgenerational epigenetic variation |
topic | Investigations |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4390564/ https://www.ncbi.nlm.nih.gov/pubmed/25617408 http://dx.doi.org/10.1534/g3.115.016725 |
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