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Genetic and epigenetic architecture of paternal origin contribute to gestation length in cattle

The length of gestation can affect offspring health and performance. Both maternal and fetal effects contribute to gestation length; however, paternal contributions to gestation length remain elusive. Using genome-wide association study (GWAS) in 27,214 Holstein bulls with millions of gestation reco...

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Autores principales: Fang, Lingzhao, Jiang, Jicai, Li, Bingjie, Zhou, Yang, Freebern, Ellen, Vanraden, Paul M., Cole, John B., Liu, George E., Ma, Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6418173/
https://www.ncbi.nlm.nih.gov/pubmed/30886909
http://dx.doi.org/10.1038/s42003-019-0341-6
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author Fang, Lingzhao
Jiang, Jicai
Li, Bingjie
Zhou, Yang
Freebern, Ellen
Vanraden, Paul M.
Cole, John B.
Liu, George E.
Ma, Li
author_facet Fang, Lingzhao
Jiang, Jicai
Li, Bingjie
Zhou, Yang
Freebern, Ellen
Vanraden, Paul M.
Cole, John B.
Liu, George E.
Ma, Li
author_sort Fang, Lingzhao
collection PubMed
description The length of gestation can affect offspring health and performance. Both maternal and fetal effects contribute to gestation length; however, paternal contributions to gestation length remain elusive. Using genome-wide association study (GWAS) in 27,214 Holstein bulls with millions of gestation records, here we identify nine paternal genomic loci associated with cattle gestation length. We demonstrate that these GWAS signals are enriched in pathways relevant to embryonic development, and in differentially methylated regions between sperm samples with long and short gestation length. We reveal that gestation length shares genetic and epigenetic architecture in sperm with calving ability, body depth, and conception rate. While several candidate genes are detected in our fine-mapping analysis, we provide evidence indicating ZNF613 as a promising candidate for cattle gestation length. Collectively, our findings support that the paternal genome and epigenome can impact gestation length potentially through regulation of the embryonic development.
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spelling pubmed-64181732019-03-18 Genetic and epigenetic architecture of paternal origin contribute to gestation length in cattle Fang, Lingzhao Jiang, Jicai Li, Bingjie Zhou, Yang Freebern, Ellen Vanraden, Paul M. Cole, John B. Liu, George E. Ma, Li Commun Biol Article The length of gestation can affect offspring health and performance. Both maternal and fetal effects contribute to gestation length; however, paternal contributions to gestation length remain elusive. Using genome-wide association study (GWAS) in 27,214 Holstein bulls with millions of gestation records, here we identify nine paternal genomic loci associated with cattle gestation length. We demonstrate that these GWAS signals are enriched in pathways relevant to embryonic development, and in differentially methylated regions between sperm samples with long and short gestation length. We reveal that gestation length shares genetic and epigenetic architecture in sperm with calving ability, body depth, and conception rate. While several candidate genes are detected in our fine-mapping analysis, we provide evidence indicating ZNF613 as a promising candidate for cattle gestation length. Collectively, our findings support that the paternal genome and epigenome can impact gestation length potentially through regulation of the embryonic development. Nature Publishing Group UK 2019-03-14 /pmc/articles/PMC6418173/ /pubmed/30886909 http://dx.doi.org/10.1038/s42003-019-0341-6 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Fang, Lingzhao
Jiang, Jicai
Li, Bingjie
Zhou, Yang
Freebern, Ellen
Vanraden, Paul M.
Cole, John B.
Liu, George E.
Ma, Li
Genetic and epigenetic architecture of paternal origin contribute to gestation length in cattle
title Genetic and epigenetic architecture of paternal origin contribute to gestation length in cattle
title_full Genetic and epigenetic architecture of paternal origin contribute to gestation length in cattle
title_fullStr Genetic and epigenetic architecture of paternal origin contribute to gestation length in cattle
title_full_unstemmed Genetic and epigenetic architecture of paternal origin contribute to gestation length in cattle
title_short Genetic and epigenetic architecture of paternal origin contribute to gestation length in cattle
title_sort genetic and epigenetic architecture of paternal origin contribute to gestation length in cattle
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6418173/
https://www.ncbi.nlm.nih.gov/pubmed/30886909
http://dx.doi.org/10.1038/s42003-019-0341-6
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