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The MBD7 complex promotes expression of methylated transgenes without significantly altering their methylation status

DNA methylation is associated with gene silencing in eukaryotic organisms. Although pathways controlling the establishment, maintenance and removal of DNA methylation are known, relatively little is understood about how DNA methylation influences gene expression. Here we identified a METHYL-CpG-BIND...

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Autores principales: Li, Dongming, Palanca, Ana Marie S, Won, So Youn, Gao, Lei, Feng, Ying, Vashisht, Ajay A, Liu, Li, Zhao, Yuanyuan, Liu, Xigang, Wu, Xiuyun, Li, Shaofang, Le, Brandon, Kim, Yun Ju, Yang, Guodong, Li, Shengben, Liu, Jinyuan, Wohlschlegel, James A, Guo, Hongwei, Mo, Beixin, Chen, Xuemei, Law, Julie A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5462541/
https://www.ncbi.nlm.nih.gov/pubmed/28452714
http://dx.doi.org/10.7554/eLife.19893
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author Li, Dongming
Palanca, Ana Marie S
Won, So Youn
Gao, Lei
Feng, Ying
Vashisht, Ajay A
Liu, Li
Zhao, Yuanyuan
Liu, Xigang
Wu, Xiuyun
Li, Shaofang
Le, Brandon
Kim, Yun Ju
Yang, Guodong
Li, Shengben
Liu, Jinyuan
Wohlschlegel, James A
Guo, Hongwei
Mo, Beixin
Chen, Xuemei
Law, Julie A
author_facet Li, Dongming
Palanca, Ana Marie S
Won, So Youn
Gao, Lei
Feng, Ying
Vashisht, Ajay A
Liu, Li
Zhao, Yuanyuan
Liu, Xigang
Wu, Xiuyun
Li, Shaofang
Le, Brandon
Kim, Yun Ju
Yang, Guodong
Li, Shengben
Liu, Jinyuan
Wohlschlegel, James A
Guo, Hongwei
Mo, Beixin
Chen, Xuemei
Law, Julie A
author_sort Li, Dongming
collection PubMed
description DNA methylation is associated with gene silencing in eukaryotic organisms. Although pathways controlling the establishment, maintenance and removal of DNA methylation are known, relatively little is understood about how DNA methylation influences gene expression. Here we identified a METHYL-CpG-BINDING DOMAIN 7 (MBD7) complex in Arabidopsis thaliana that suppresses the transcriptional silencing of two LUCIFERASE (LUC) reporters via a mechanism that is largely downstream of DNA methylation. Although mutations in components of the MBD7 complex resulted in modest increases in DNA methylation concomitant with decreased LUC expression, we found that these hyper-methylation and gene expression phenotypes can be genetically uncoupled. This finding, along with genome-wide profiling experiments showing minimal changes in DNA methylation upon disruption of the MBD7 complex, places the MBD7 complex amongst a small number of factors acting downstream of DNA methylation. This complex, however, is unique as it functions to suppress, rather than enforce, DNA methylation-mediated gene silencing. DOI: http://dx.doi.org/10.7554/eLife.19893.001
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spelling pubmed-54625412017-06-09 The MBD7 complex promotes expression of methylated transgenes without significantly altering their methylation status Li, Dongming Palanca, Ana Marie S Won, So Youn Gao, Lei Feng, Ying Vashisht, Ajay A Liu, Li Zhao, Yuanyuan Liu, Xigang Wu, Xiuyun Li, Shaofang Le, Brandon Kim, Yun Ju Yang, Guodong Li, Shengben Liu, Jinyuan Wohlschlegel, James A Guo, Hongwei Mo, Beixin Chen, Xuemei Law, Julie A eLife Genes and Chromosomes DNA methylation is associated with gene silencing in eukaryotic organisms. Although pathways controlling the establishment, maintenance and removal of DNA methylation are known, relatively little is understood about how DNA methylation influences gene expression. Here we identified a METHYL-CpG-BINDING DOMAIN 7 (MBD7) complex in Arabidopsis thaliana that suppresses the transcriptional silencing of two LUCIFERASE (LUC) reporters via a mechanism that is largely downstream of DNA methylation. Although mutations in components of the MBD7 complex resulted in modest increases in DNA methylation concomitant with decreased LUC expression, we found that these hyper-methylation and gene expression phenotypes can be genetically uncoupled. This finding, along with genome-wide profiling experiments showing minimal changes in DNA methylation upon disruption of the MBD7 complex, places the MBD7 complex amongst a small number of factors acting downstream of DNA methylation. This complex, however, is unique as it functions to suppress, rather than enforce, DNA methylation-mediated gene silencing. DOI: http://dx.doi.org/10.7554/eLife.19893.001 eLife Sciences Publications, Ltd 2017-04-28 /pmc/articles/PMC5462541/ /pubmed/28452714 http://dx.doi.org/10.7554/eLife.19893 Text en © 2017, Li 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 Genes and Chromosomes
Li, Dongming
Palanca, Ana Marie S
Won, So Youn
Gao, Lei
Feng, Ying
Vashisht, Ajay A
Liu, Li
Zhao, Yuanyuan
Liu, Xigang
Wu, Xiuyun
Li, Shaofang
Le, Brandon
Kim, Yun Ju
Yang, Guodong
Li, Shengben
Liu, Jinyuan
Wohlschlegel, James A
Guo, Hongwei
Mo, Beixin
Chen, Xuemei
Law, Julie A
The MBD7 complex promotes expression of methylated transgenes without significantly altering their methylation status
title The MBD7 complex promotes expression of methylated transgenes without significantly altering their methylation status
title_full The MBD7 complex promotes expression of methylated transgenes without significantly altering their methylation status
title_fullStr The MBD7 complex promotes expression of methylated transgenes without significantly altering their methylation status
title_full_unstemmed The MBD7 complex promotes expression of methylated transgenes without significantly altering their methylation status
title_short The MBD7 complex promotes expression of methylated transgenes without significantly altering their methylation status
title_sort mbd7 complex promotes expression of methylated transgenes without significantly altering their methylation status
topic Genes and Chromosomes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5462541/
https://www.ncbi.nlm.nih.gov/pubmed/28452714
http://dx.doi.org/10.7554/eLife.19893
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