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Inducible cell-specific mouse models for paired epigenetic and transcriptomic studies of microglia and astroglia.
Chucair-Elliott, Ana J; Ocañas, Sarah R; Stanford, David R; Ansere, Victor A; Buettner, Kyla B; Porter, Hunter; Eliason, Nicole L; Reid, Justin J; Sharpe, Amanda L; Stout, Michael B; Beckstead, Michael J; Miller, Benjamin F; Richardson, Arlan; Freeman, Willard M.
Affiliation
  • Chucair-Elliott AJ; Genes & Human Disease Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, USA.
  • Ocañas SR; Genes & Human Disease Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, USA.
  • Stanford DR; Department of Physiology, University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA.
  • Ansere VA; Genes & Human Disease Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, USA.
  • Buettner KB; Genes & Human Disease Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, USA.
  • Porter H; Department of Physiology, University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA.
  • Eliason NL; Genes & Human Disease Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, USA.
  • Reid JJ; Department of Physiology, University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA.
  • Sharpe AL; Genes & Human Disease Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, USA.
  • Stout MB; Oklahoma Center for Neuroscience, University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA.
  • Beckstead MJ; Department of Pharmaceutical Sciences, University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA.
  • Miller BF; Aging & Metabolism Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, USA.
  • Richardson A; Department of Pharmaceutical Sciences, University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA.
  • Freeman WM; Department of Nutritional Sciences, University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA.
Commun Biol ; 3(1): 693, 2020 11 19.
Article in En | MEDLINE | ID: mdl-33214681
ABSTRACT
Epigenetic regulation of gene expression occurs in a cell type-specific manner. Current cell-type specific neuroepigenetic studies rely on cell sorting methods that can alter cell phenotype and introduce potential confounds. Here we demonstrate and validate a Nuclear Tagging and Translating Ribosome Affinity Purification (NuTRAP) approach for temporally controlled labeling and isolation of ribosomes and nuclei, and thus RNA and DNA, from specific central nervous system cell types. Analysis of gene expression and DNA modifications in astrocytes or microglia from the same animal demonstrates differential usage of DNA methylation and hydroxymethylation in CpG and non-CpG contexts that corresponds to cell type-specific gene expression. Application of this approach in LPS treated mice uncovers microglia-specific transcriptome and epigenome changes in inflammatory pathways that cannot be detected with tissue-level analysis. The NuTRAP model and the validation approaches presented can be applied to any brain cell type for which a cell type-specific cre is available.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Astrocytes / Microglia / Epigenesis, Genetic / Transcriptome Limits: Animals Language: En Journal: Commun Biol Year: 2020 Document type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Astrocytes / Microglia / Epigenesis, Genetic / Transcriptome Limits: Animals Language: En Journal: Commun Biol Year: 2020 Document type: Article Affiliation country: United States