Epigenetic reprogramming in pancreatic acinar cell in the absence of MIST1
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ABSTRACT: Epigenetic profile of tissues is reprogrammed under diseased conditions. H3K4Me3 and H3K27Me3 represent active and repressive epigenetic marks, respectively. ChIP-seq is an effective tool to study global protein-DNA interactions. To study global epigenetic differences, we used H3K4Me3 antibody to evaluate its enrichment in pancreatic acinar cells of WT and Mist1-/- mice followed by next generation sequencing. We found specific hotspots that showed differential enrichment for H3K4Me3 both in WT and Mist1-/- mice. The data show that pancreatic acinar cells are epigenetically reprogrammed under stressed cellular conditions. Global H3K4Me3 profiling of WT and Mist1-/- pancreatic acinar cells using ChIP-seq.
ORGANISM(S): Mus musculus
SUBMITTER: Christopher Pin
PROVIDER: E-GEOD-49113 | biostudies-arrayexpress |
REPOSITORIES: biostudies-arrayexpress
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