Nature communications · 2016
Integrative epigenome-wide analysis demonstrates that DNA methylation may mediate genetic risk in inflammatory bowel disease.
СтатьяПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод пока не подготовлен
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Ventham N T, Kennedy N A, Adams A T, Kalla R, Heath S, O'Leary K R, Drummond H, IBD BIOM consortium, IBD CHARACTER consortium, Wilson D C, Gut I G, Nimmo E R, Satsangi J
Аннотация
Epigenetic alterations may provide important insights into gene-environment interaction in inflammatory bowel disease (IBD). Here we observe epigenome-wide DNA methylation differences in 240 newly-diagnosed IBD cases and 190 controls. These include 439 differentially methylated positions (DMPs) and 5 differentially methylated regions (DMRs), which we study in detail using whole genome bisulphite sequencing. We replicate the top DMP (RPS6KA2) and DMRs (VMP1, ITGB2 and TXK) in an independent cohort. Using paired genetic and epigenetic data, we delineate methylation quantitative trait loci; VMP1/microRNA-21 methylation associates with two polymorphisms in linkage disequilibrium with a known IBD susceptibility variant. Separated cell data shows that IBD-associated hypermethylation within the TXK promoter region negatively correlates with gene expression in whole-blood and CD8+ T cells, but not other cell types. Thus, site-specific DNA methylation changes in IBD relate to underlying genotype and associate with cell-specific alteration in gene expression.
Предметные рубрики MeSH
AdultCase-Control StudiesCohort StudiesColitis, UlcerativeCrohn DiseaseDNA MethylationEpigenesis, GeneticEpigenomicsFemaleGene Expression ProfilingGene-Environment InteractionGenetic Predisposition to DiseaseGenotypeHumansLinkage DisequilibriumMaleMembrane ProteinsMicroRNAsMiddle AgedPolymorphism, Single NucleotidePromoter Regions, GeneticProtein-Tyrosine KinasesQuantitative Trait Loci