GRO-seq from HCT116 cells
Source: NCBI BioProject (ID PRJNA167277)

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Project name: Homo sapiens
Description: The majority of transcription studies examine steady-state RNA . However steady-state RNA is not a true reflection of the transcriptome, because the RNA levels are affected by both transcription rate and degradation rate. In this experiment we measured the amount of transcription occurring in HCT116 colon cancer cells, regardless of degradation, using GRO-seq (global nuclear run-on sequencing). This information demonstrates that many genes have a pile-up of transcriptionally-engaged polymerase near their 5'-end.Overall design: Nuclei were prepared from HCT116 cells (treated for 1hr with DMSO as control for additional GRO-seq experiments to be reported separately). Transcription run-on was performed (as per Core, L.J., Waterfall, J.J., and Lis, J.T. (2008). Nascent RNA sequencing reveals widespread pausing and divergent initiation at human promoters. Science 322, 1845-1848) and nascent RNAs were purified and sequenced.
Data type: Other
Sample scope: Monoisolate
Relevance: Medical
Organization: Pharmacology & Linda Crnic Institute for Down Syndrome, University of Colorado Anschutz Medical Campus
Literatures
  1. PMID: 23746844
Last updated: 2012-05-22
Statistics: 1 sample; 1 experiment; 3 runs