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dc.contributor.authorPicard, Colette Lafontaine
dc.contributor.authorGehring, Mary
dc.date.accessioned2018-06-20T13:45:39Z
dc.date.available2018-06-20T13:45:39Z
dc.date.issued2017-04
dc.date.submitted2017-01
dc.identifier.issn1474-760X
dc.identifier.urihttp://hdl.handle.net/1721.1/116446
dc.description.abstractBackground: Gene body methylation at CG dinucleotides is a widely conserved feature of methylated genomes but remains poorly understood. The Arabidopsis thaliana strain Cvi has depleted gene body methylation relative to the reference strain Col. Here, we leverage this natural epigenetic difference to investigate gene body methylation stability. Results: Recombinant inbred lines derived from Col and Cvi were used to examine the transmission of distinct gene body methylation states. The vast majority of genic CG methylation patterns are faithfully transmitted over nine generations according to parental genotype, with only 1-4% of CGs either losing or gaining methylation relative to the parent. Genic CGs that fail to maintain the parental methylation state are shared among independent lines, suggesting that these are not random occurrences. We use a logistic regression framework to identify features that best predict sites that fail to maintain parental methylation state. Intermediate levels of CG methylation around a dynamic CG site and high methylation variability across many A. thaliana strains at that site are the strongest predictors. These data suggest that the dynamic CGs we identify are not specific to the Col-Cvi recombinant inbred lines but have an epigenetic state that is inherently less stable within the A. thaliana species. Extending this, variably methylated genic CGs in maize and Brachypodium distachyon are also associated with intermediate local CG methylation. Conclusions: These results provide new insights into the features determining the inheritance of gene body methylation and demonstrate that two different methylation equilibria can be maintained within single individuals.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant T32 GM087237)en_US
dc.publisherBiomed Central Ltden_US
dc.relation.isversionofhttp://dx.doi.org/10.1186/S13059-017-1206-2en_US
dc.rightsCreative Commons Attribution 4.0 International Licenseen_US
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_US
dc.sourceBioMedCentralen_US
dc.titleProximal methylation features associated with nonrandom changes in gene body methylationen_US
dc.typeArticleen_US
dc.identifier.citationPicard, Colette L. and Mary Gehring. “Proximal Methylation Features Associated with Nonrandom Changes in Gene Body Methylation.” Genome Biology 18, 1 (April 2017): 73 © 2017 The Author(s)en_US
dc.contributor.departmentMassachusetts Institute of Technology. Computational and Systems Biology Programen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.contributor.mitauthorPicard, Colette Lafontaine
dc.contributor.mitauthorGehring, Mary
dc.relation.journalGenome Biologyen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2018-06-15T19:32:27Z
dspace.orderedauthorsPicard, Colette L.; Gehring, Maryen_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0002-2177-2216
dc.identifier.orcidhttps://orcid.org/0000-0003-2280-1522
mit.licensePUBLISHER_CCen_US


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