| Literature DB >> 27851968 |
Davide Pellacani1, Misha Bilenky2, Nagarajan Kannan1, Alireza Heravi-Moussavi2, David J H F Knapp1, Sitanshu Gakkhar2, Michelle Moksa3, Annaick Carles3, Richard Moore2, Andrew J Mungall2, Marco A Marra2, Steven J M Jones2, Samuel Aparicio4, Martin Hirst5, Connie J Eaves6.
Abstract
The normal adult human mammary gland is a continuous bilayered epithelial system. Bipotent and myoepithelial progenitors are prominent and unique components of the outer (basal) layer. The inner (luminal) layer includes both luminal-restricted progenitors and a phenotypically separable fraction that lacks progenitor activity. We now report an epigenomic comparison of these three subsets with one another, with their associated stromal cells, and with three immortalized, non-tumorigenic human mammary cell lines. Each genome-wide analysis contains profiles for six histone marks, methylated DNA, and RNA transcripts. Analysis of these datasets shows that each cell type has unique features, primarily within genomic regulatory regions, and that the cell lines group together. Analyses of the promoter and enhancer profiles place the luminal progenitors in between the basal cells and the non-progenitor luminal subset. Integrative analysis reveals networks of subset-specific transcription factors.Entities:
Keywords: chromatin; enhancer; epigenomic; mammary cells; normal human breast; profiling; regulatory network; stem cells; transcription factors; transcriptome
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Year: 2016 PMID: 27851968 DOI: 10.1016/j.celrep.2016.10.058
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423