Metabolomics,Unknown,Transcriptomics,Genomics,Proteomics

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Transcriptional response to stress in serum deprived mouse fibroblasts in the presence of MSK1/2 inhibitor.


ABSTRACT: We have employed gene expression profiling in order to identify targets of transcriptional response to stress in resting mouse Swiss 3T3 fibroblasts, either untreated (control) or treated with anisomycin for 3 or 6 hours to induce the p38/MAP kinase pathway. In order determine transcriptional effects dependent on MSK1/2 kinase activity, H89 inhibitor was used in the study. Serum starved (72 h 0.2% FCS) mouse 3T3 cells were treated with anisomycin (188.5 nM) for 3 h or 6h (in duplicates) either with or without 15-min pre-treatment with MSK1/2 inhibitor H89 (10 uM). Untreated, serum-starved cells were used as a control. RNA was collected and gene expression profiling using strand-specific RNA-seq was performed.

ORGANISM(S): Mus musculus

SUBMITTER: Anna Sawicka 

PROVIDER: E-GEOD-58746 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress

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Publications

H3S28 phosphorylation is a hallmark of the transcriptional response to cellular stress.

Sawicka Anna A   Hartl Dominik D   Goiser Malgorzata M   Pusch Oliver O   Stocsits Roman R RR   Tamir Ido M IM   Mechtler Karl K   Seiser Christian C  

Genome research 20140818 11


The selectivity of transcriptional responses to extracellular cues is reflected by the deposition of stimulus-specific chromatin marks. Although histone H3 phosphorylation is a target of numerous signaling pathways, its role in transcriptional regulation remains poorly understood. Here, for the first time, we report a genome-wide analysis of H3S28 phosphorylation in a mammalian system in the context of stress signaling. We found that this mark targets as many as 50% of all stress-induced genes,  ...[more]

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