Author
Listed:
- Xiao-Long Cui
(University of Chicago
University of Chicago)
- Ji Nie
(University of Chicago
University of Chicago)
- Jeremy Ku
(Bluestar Genomics Inc.)
- Urszula Dougherty
(University of Chicago)
- Diana C. West-Szymanski
(University of Chicago
University of Chicago)
- Francois Collin
(Bluestar Genomics Inc.)
- Christopher K. Ellison
(Bluestar Genomics Inc.)
- Laura Sieh
(University of Chicago
University of Chicago)
- Yuhong Ning
(Bluestar Genomics Inc.)
- Zifeng Deng
(University of Chicago)
- Carolyn W. T. Zhao
(University of Chicago
University of Chicago)
- Anna Bergamaschi
(Bluestar Genomics Inc.)
- Joel Pekow
(University of Chicago)
- Jiangbo Wei
(University of Chicago
University of Chicago)
- Alana V. Beadell
(University of Chicago
University of Chicago)
- Zhou Zhang
(Northwestern University Feinberg School of Medicine)
- Geeta Sharma
(City of Hope Comprehensive Cancer Center)
- Raman Talwar
(Bluestar Genomics Inc.)
- Patrick Arensdorf
(Bluestar Genomics Inc.)
- Jason Karpus
(University of Chicago
University of Chicago)
- Ajay Goel
(City of Hope Comprehensive Cancer Center)
- Marc Bissonnette
(University of Chicago)
- Wei Zhang
(Northwestern University Feinberg School of Medicine)
- Samuel Levy
(Bluestar Genomics Inc.)
- Chuan He
(University of Chicago
University of Chicago)
Abstract
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.
Suggested Citation
Xiao-Long Cui & Ji Nie & Jeremy Ku & Urszula Dougherty & Diana C. West-Szymanski & Francois Collin & Christopher K. Ellison & Laura Sieh & Yuhong Ning & Zifeng Deng & Carolyn W. T. Zhao & Anna Bergama, 2020.
"A human tissue map of 5-hydroxymethylcytosines exhibits tissue specificity through gene and enhancer modulation,"
Nature Communications, Nature, vol. 11(1), pages 1-11, December.
Handle:
RePEc:nat:natcom:v:11:y:2020:i:1:d:10.1038_s41467-020-20001-w
DOI: 10.1038/s41467-020-20001-w
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