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A human tissue map of 5-hydroxymethylcytosines exhibits tissue specificity through gene and enhancer modulation.

Xiao-Long CuiJi NieJeremy KuUrszula DoughertyDiana C West-SzymanskiFrancois CollinChristopher K EllisonLaura SiehYuhong NingZifeng DengCarolyn W T ZhaoAnna BergamaschiJoel PekowJiangbo WeiAlana V BeadellSheng ZhangGeeta Geeta SharmaRaman TalwarPatrick ArensdorfJason KarpusAjay GoelMarc BissonnetteTripti KhareSamuel LevyChuan He
Published in: Nature communications (2020)
DNA 5-hydroxymethylcytosine (5hmC) modification is known to be associated with gene transcription and frequently used as a mark to investigate dynamic DNA methylation conversion during mammalian development and in human diseases. However, the lack of genome-wide 5hmC profiles in different human tissue types impedes drawing generalized conclusions about how 5hmC is implicated in transcription activity and tissue specificity. To meet this need, we describe the development of a 5hmC tissue map by characterizing the genomic distributions of 5hmC in 19 human tissues derived from ten organ systems. Subsequent sequencing results enabled the identification of genome-wide 5hmC distributions that uniquely separates samples by tissue type. Further comparison of the 5hmC profiles with transcriptomes and histone modifications revealed that 5hmC is preferentially enriched on tissue-specific gene bodies and enhancers. Taken together, the results provide an extensive 5hmC map across diverse human tissue types that suggests a potential role of 5hmC in tissue-specific development; as well as a resource to facilitate future studies of DNA demethylation in pathogenesis and the development of 5hmC as biomarkers.
Keyphrases
  • genome wide
  • dna methylation
  • endothelial cells
  • copy number
  • induced pluripotent stem cells
  • pluripotent stem cells
  • gene expression
  • single cell
  • binding protein
  • circulating tumor cells
  • structural basis