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Characterizing Genetic Regulatory Elements in Ovine Tissues

The Ovine Functional Annotation of Animal Genomes (FAANG) project, part of the broader livestock species FAANG initiative, aims to identify and characterize gene regulatory elements in domestic sheep. Regulatory element annotation is essential for identifying genetic variants that affect health and...

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Autores principales: Davenport, Kimberly M., Massa, Alisha T., Bhattarai, Suraj, McKay, Stephanie D., Mousel, Michelle R., Herndon, Maria K., White, Stephen N., Cockett, Noelle E., Smith, Timothy P. L., Murdoch, Brenda M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8173140/
https://www.ncbi.nlm.nih.gov/pubmed/34093640
http://dx.doi.org/10.3389/fgene.2021.628849
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author Davenport, Kimberly M.
Massa, Alisha T.
Bhattarai, Suraj
McKay, Stephanie D.
Mousel, Michelle R.
Herndon, Maria K.
White, Stephen N.
Cockett, Noelle E.
Smith, Timothy P. L.
Murdoch, Brenda M.
author_facet Davenport, Kimberly M.
Massa, Alisha T.
Bhattarai, Suraj
McKay, Stephanie D.
Mousel, Michelle R.
Herndon, Maria K.
White, Stephen N.
Cockett, Noelle E.
Smith, Timothy P. L.
Murdoch, Brenda M.
author_sort Davenport, Kimberly M.
collection PubMed
description The Ovine Functional Annotation of Animal Genomes (FAANG) project, part of the broader livestock species FAANG initiative, aims to identify and characterize gene regulatory elements in domestic sheep. Regulatory element annotation is essential for identifying genetic variants that affect health and production traits in this important agricultural species, as greater than 90% of variants underlying genetic effects are estimated to lie outside of transcribed regions. Histone modifications that distinguish active or repressed chromatin states, CTCF binding, and DNA methylation were used to characterize regulatory elements in liver, spleen, and cerebellum tissues from four yearling sheep. Chromatin immunoprecipitation with sequencing (ChIP-seq) was performed for H3K4me3, H3K27ac, H3K4me1, H3K27me3, and CTCF. Nine chromatin states including active promoters, active enhancers, poised enhancers, repressed enhancers, and insulators were characterized in each tissue using ChromHMM. Whole-genome bisulfite sequencing (WGBS) was performed to determine the complement of whole-genome DNA methylation with the ChIP-seq data. Hypermethylated and hypomethylated regions were identified across tissues, and these locations were compared with chromatin states to better distinguish and validate regulatory elements in these tissues. Interestingly, chromatin states with the poised enhancer mark H3K4me1 in the spleen and cerebellum and CTCF in the liver displayed the greatest number of hypermethylated sites. Not surprisingly, active enhancers in the liver and spleen, and promoters in the cerebellum, displayed the greatest number of hypomethylated sites. Overall, chromatin states defined by histone marks and CTCF occupied approximately 22% of the genome in all three tissues. Furthermore, the liver and spleen displayed in common the greatest percent of active promoter (65%) and active enhancer (81%) states, and the liver and cerebellum displayed in common the greatest percent of poised enhancer (53%), repressed enhancer (68%), hypermethylated sites (75%), and hypomethylated sites (73%). In addition, both known and de novo CTCF-binding motifs were identified in all three tissues, with the highest number of unique motifs identified in the cerebellum. In summary, this study has identified the regulatory regions of genes in three tissues that play key roles in defining health and economically important traits and has set the precedent for the characterization of regulatory elements in ovine tissues using the Rambouillet reference genome.
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spelling pubmed-81731402021-06-04 Characterizing Genetic Regulatory Elements in Ovine Tissues Davenport, Kimberly M. Massa, Alisha T. Bhattarai, Suraj McKay, Stephanie D. Mousel, Michelle R. Herndon, Maria K. White, Stephen N. Cockett, Noelle E. Smith, Timothy P. L. Murdoch, Brenda M. Front Genet Genetics The Ovine Functional Annotation of Animal Genomes (FAANG) project, part of the broader livestock species FAANG initiative, aims to identify and characterize gene regulatory elements in domestic sheep. Regulatory element annotation is essential for identifying genetic variants that affect health and production traits in this important agricultural species, as greater than 90% of variants underlying genetic effects are estimated to lie outside of transcribed regions. Histone modifications that distinguish active or repressed chromatin states, CTCF binding, and DNA methylation were used to characterize regulatory elements in liver, spleen, and cerebellum tissues from four yearling sheep. Chromatin immunoprecipitation with sequencing (ChIP-seq) was performed for H3K4me3, H3K27ac, H3K4me1, H3K27me3, and CTCF. Nine chromatin states including active promoters, active enhancers, poised enhancers, repressed enhancers, and insulators were characterized in each tissue using ChromHMM. Whole-genome bisulfite sequencing (WGBS) was performed to determine the complement of whole-genome DNA methylation with the ChIP-seq data. Hypermethylated and hypomethylated regions were identified across tissues, and these locations were compared with chromatin states to better distinguish and validate regulatory elements in these tissues. Interestingly, chromatin states with the poised enhancer mark H3K4me1 in the spleen and cerebellum and CTCF in the liver displayed the greatest number of hypermethylated sites. Not surprisingly, active enhancers in the liver and spleen, and promoters in the cerebellum, displayed the greatest number of hypomethylated sites. Overall, chromatin states defined by histone marks and CTCF occupied approximately 22% of the genome in all three tissues. Furthermore, the liver and spleen displayed in common the greatest percent of active promoter (65%) and active enhancer (81%) states, and the liver and cerebellum displayed in common the greatest percent of poised enhancer (53%), repressed enhancer (68%), hypermethylated sites (75%), and hypomethylated sites (73%). In addition, both known and de novo CTCF-binding motifs were identified in all three tissues, with the highest number of unique motifs identified in the cerebellum. In summary, this study has identified the regulatory regions of genes in three tissues that play key roles in defining health and economically important traits and has set the precedent for the characterization of regulatory elements in ovine tissues using the Rambouillet reference genome. Frontiers Media S.A. 2021-05-20 /pmc/articles/PMC8173140/ /pubmed/34093640 http://dx.doi.org/10.3389/fgene.2021.628849 Text en Copyright © 2021 Davenport, Massa, Bhattarai, McKay, Mousel, Herndon, White, Cockett, Smith and Murdoch. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Davenport, Kimberly M.
Massa, Alisha T.
Bhattarai, Suraj
McKay, Stephanie D.
Mousel, Michelle R.
Herndon, Maria K.
White, Stephen N.
Cockett, Noelle E.
Smith, Timothy P. L.
Murdoch, Brenda M.
Characterizing Genetic Regulatory Elements in Ovine Tissues
title Characterizing Genetic Regulatory Elements in Ovine Tissues
title_full Characterizing Genetic Regulatory Elements in Ovine Tissues
title_fullStr Characterizing Genetic Regulatory Elements in Ovine Tissues
title_full_unstemmed Characterizing Genetic Regulatory Elements in Ovine Tissues
title_short Characterizing Genetic Regulatory Elements in Ovine Tissues
title_sort characterizing genetic regulatory elements in ovine tissues
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8173140/
https://www.ncbi.nlm.nih.gov/pubmed/34093640
http://dx.doi.org/10.3389/fgene.2021.628849
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