Discovering Transcriptional Regulatory Elements From Run-On and Sequencing Data Using the Web-Based dREG Gateway

Curr Protoc Bioinformatics. 2019 Jun;66(1):e70. doi: 10.1002/cpbi.70. Epub 2018 Dec 27.

Abstract

Transcription is a chromatin mark that can be used effectively to identify the location of active enhancers and promoters, collectively known as transcriptional regulatory elements (TREs). We recently introduced dREG, a tool for the identification of TREs using run-on and sequencing (RO-seq) assays, including global run-on and sequencing (GRO-seq), precision run-on and sequencing (PRO-seq), and chromatin run-on and sequencing (ChRO-seq). In this protocol, we present step-by-step instructions for running dREG on an arbitrary run-on and sequencing dataset. Users provide dREG with bigWig files (in which each read is represented by a single base) representing the location of RNA polymerase in a cell or tissue sample of interest, and dREG returns a list of genomic regions that are predicted to be active TREs. Finally, we demonstrate the use of dREG regions in discovering transcription factors controlling response to a stimulus and predicting their target genes. Together, this protocol provides detailed instructions for running dREG on arbitrary run-on and sequencing data. © 2018 by John Wiley & Sons, Inc.

Keywords: ChRO-seq; GRO-seq; PRO-seq; enhancers; gene regulation.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Base Sequence
  • Genome
  • Internet*
  • Ionomycin / pharmacology
  • Nucleotide Motifs / genetics
  • Regulatory Elements, Transcriptional / genetics*
  • Sequence Analysis, RNA*
  • Software*
  • Tetradecanoylphorbol Acetate / pharmacology
  • Transcription Factors / genetics

Substances

  • Transcription Factors
  • Ionomycin
  • Tetradecanoylphorbol Acetate