Epigenomic analysis of multilineage differentiation of human embryonic stem cells.

TitleEpigenomic analysis of multilineage differentiation of human embryonic stem cells.
Publication TypeJournal Article
Year of Publication2013
AuthorsXie W, Schultz MD, Lister R, Hou Z, Rajagopal N, Ray P, Whitaker JW, Tian S, Hawkins DR, Leung D, Yang H, Wang T, Lee A Y, Swanson SA, Zhang J, Zhu Y, Kim A, Nery JR, Urich MA, Kuan S, Yen C-an, Klugman S, Yu P, Suknuntha K, Propson NE, Chen H, Edsall LE, Wagner U, Li Y, Ye Z, Kulkarni A, Xuan Z, Chung W-Y, Chi NC, Antosiewicz-Bourget JE, Slukvin I, Stewart R, Zhang MQ, Wang W, Thomson JA, Ecker JR, Ren B
Date Published2013 May 23
KeywordsAnimals, Cell Differentiation, Chromatin, CpG Islands, DNA Methylation, Embryonic Stem Cells, Epigenomics, Gene Expression Regulation, Developmental, Histones, Humans, Methylation, Neoplasms, Promoter Regions, Genetic, Zebrafish

Epigenetic mechanisms have been proposed to play crucial roles in mammalian development, but their precise functions are only partially understood. To investigate epigenetic regulation of embryonic development, we differentiated human embryonic stem cells into mesendoderm, neural progenitor cells, trophoblast-like cells, and mesenchymal stem cells and systematically characterized DNA methylation, chromatin modifications, and the transcriptome in each lineage. We found that promoters that are active in early developmental stages tend to be CG rich and mainly engage H3K27me3 upon silencing in nonexpressing lineages. By contrast, promoters for genes expressed preferentially at later stages are often CG poor and primarily employ DNA methylation upon repression. Interestingly, the early developmental regulatory genes are often located in large genomic domains that are generally devoid of DNA methylation in most lineages, which we termed DNA methylation valleys (DMVs). Our results suggest that distinct epigenetic mechanisms regulate early and late stages of ES cell differentiation.

PubMed URLhttp://www.ncbi.nlm.nih.gov/pubmed/23664764?dopt=Abstract
Alternate TitleCell
PubMed ID23664764