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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2016
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
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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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