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Epigenomic landscapes of retinal rods and cones
Rod and cone photoreceptors are highly similar in many respects but they have important functional and molecular differences. Here, we investigate genome-wide patterns of DNA methylation and chromatin accessibility in mouse rods and cones and correlate differences in these features with gene express...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4798964/ https://www.ncbi.nlm.nih.gov/pubmed/26949250 http://dx.doi.org/10.7554/eLife.11613 |
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author | Mo, Alisa Luo, Chongyuan Davis, Fred P Mukamel, Eran A Henry, Gilbert L Nery, Joseph R Urich, Mark A Picard, Serge Lister, Ryan Eddy, Sean R Beer, Michael A Ecker, Joseph R Nathans, Jeremy |
author_facet | Mo, Alisa Luo, Chongyuan Davis, Fred P Mukamel, Eran A Henry, Gilbert L Nery, Joseph R Urich, Mark A Picard, Serge Lister, Ryan Eddy, Sean R Beer, Michael A Ecker, Joseph R Nathans, Jeremy |
author_sort | Mo, Alisa |
collection | PubMed |
description | Rod and cone photoreceptors are highly similar in many respects but they have important functional and molecular differences. Here, we investigate genome-wide patterns of DNA methylation and chromatin accessibility in mouse rods and cones and correlate differences in these features with gene expression, histone marks, transcription factor binding, and DNA sequence motifs. Loss of NR2E3 in rods shifts their epigenomes to a more cone-like state. The data further reveal wide differences in DNA methylation between retinal photoreceptors and brain neurons. Surprisingly, we also find a substantial fraction of DNA hypo-methylated regions in adult rods that are not in active chromatin. Many of these regions exhibit hallmarks of regulatory regions that were active earlier in neuronal development, suggesting that these regions could remain undermethylated due to the highly compact chromatin in mature rods. This work defines the epigenomic landscapes of rods and cones, revealing features relevant to photoreceptor development and function. DOI: http://dx.doi.org/10.7554/eLife.11613.001 |
format | Online Article Text |
id | pubmed-4798964 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-47989642016-03-21 Epigenomic landscapes of retinal rods and cones Mo, Alisa Luo, Chongyuan Davis, Fred P Mukamel, Eran A Henry, Gilbert L Nery, Joseph R Urich, Mark A Picard, Serge Lister, Ryan Eddy, Sean R Beer, Michael A Ecker, Joseph R Nathans, Jeremy eLife Genomics and Evolutionary Biology Rod and cone photoreceptors are highly similar in many respects but they have important functional and molecular differences. Here, we investigate genome-wide patterns of DNA methylation and chromatin accessibility in mouse rods and cones and correlate differences in these features with gene expression, histone marks, transcription factor binding, and DNA sequence motifs. Loss of NR2E3 in rods shifts their epigenomes to a more cone-like state. The data further reveal wide differences in DNA methylation between retinal photoreceptors and brain neurons. Surprisingly, we also find a substantial fraction of DNA hypo-methylated regions in adult rods that are not in active chromatin. Many of these regions exhibit hallmarks of regulatory regions that were active earlier in neuronal development, suggesting that these regions could remain undermethylated due to the highly compact chromatin in mature rods. This work defines the epigenomic landscapes of rods and cones, revealing features relevant to photoreceptor development and function. DOI: http://dx.doi.org/10.7554/eLife.11613.001 eLife Sciences Publications, Ltd 2016-03-07 /pmc/articles/PMC4798964/ /pubmed/26949250 http://dx.doi.org/10.7554/eLife.11613 Text en © 2016, Mo et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Genomics and Evolutionary Biology Mo, Alisa Luo, Chongyuan Davis, Fred P Mukamel, Eran A Henry, Gilbert L Nery, Joseph R Urich, Mark A Picard, Serge Lister, Ryan Eddy, Sean R Beer, Michael A Ecker, Joseph R Nathans, Jeremy Epigenomic landscapes of retinal rods and cones |
title | Epigenomic landscapes of retinal rods and cones |
title_full | Epigenomic landscapes of retinal rods and cones |
title_fullStr | Epigenomic landscapes of retinal rods and cones |
title_full_unstemmed | Epigenomic landscapes of retinal rods and cones |
title_short | Epigenomic landscapes of retinal rods and cones |
title_sort | epigenomic landscapes of retinal rods and cones |
topic | Genomics and Evolutionary Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4798964/ https://www.ncbi.nlm.nih.gov/pubmed/26949250 http://dx.doi.org/10.7554/eLife.11613 |
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