| Literature DB >> 28122230 |
Hyun Cheol Roh1, Linus T-Y Tsai1, Anna Lyubetskaya1, Danielle Tenen1, Manju Kumari1, Evan D Rosen2.
Abstract
Epigenomic mechanisms direct distinct gene expression programs for different cell types. Various in vivo tissues have been subjected to epigenomic analysis; however, these studies have been limited by cellular heterogeneity, resulting in composite gene expression and epigenomic profiles. Here, we introduce "NuTRAP," a transgenic mouse that allows simultaneous isolation of cell-type-specific translating mRNA and chromatin from complex tissues. Using NuTRAP, we successfully characterize gene expression and epigenomic states of various adipocyte populations in vivo, revealing significant differences compared to either whole adipose tissue or in vitro adipocyte cell lines. We find that chromatin immunoprecipitation sequencing (ChIP-seq) using NuTRAP is highly efficient, scalable, and robust with even limited cell input. We further demonstrate the general utility of NuTRAP by analyzing hepatocyte-specific epigenomic states. The NuTRAP mouse is a resource that provides a powerful system for cell-type-specific gene expression and epigenomic profiling.Entities:
Keywords: ChIP-seq; NuTRAP; RNA-seq; adipocyte; epigenomics
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Year: 2017 PMID: 28122230 PMCID: PMC5291126 DOI: 10.1016/j.celrep.2016.12.087
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423