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SRX3796972: GSM3043142: Lrp::kanR Minimal logarithmic rep2-RNAseq; Escherichia coli; RNA-Seq
1 ILLUMINA (NextSeq 500) run: 5.9M spots, 445.8M bases, 141.9Mb downloads

Submitted by: NCBI (GEO)
Study: Escherichia coli Lrp regulates one-third of the genome via direct, cooperative, and indirect paths
show Abstracthide Abstract
The global regulator Lrp plays a crucial role in regulating metabolism, virulence and motility in response to environmental conditions.  Lrp has previously been shown to activate or repress approximately 10% of genes in Escherichia coli.  However, the full spectrum of targets, and how Lrp acts to regulate them, has stymied earlier study.  We have combined matched ChIP-seq and RNA sequencing under nine physiological conditions to map the binding and regulatory activity of Lrp as it directs responses to nutrient abundance. In addition to identifying hundreds of novel Lrp targets, we observe two new global trends: first, that Lrp will often bind to promoters in a poised position under conditions when it has no regulatory activity, and second, that nutrient levels induce a global shift in the equilibrium between non-specific and sequence-specific DNA binding.  The overall regulatory behavior of Lrp, which as we now show regulates 35% of E. coli genes directly or indirectly under at least one condition, thus arises from the interaction between changes in Lrp binding specificity and cooperative action with other regulators. Overall design: Profiles of Lrp binding and global transcription levels determined under nine conditions with duplicates in WT and Lrp::kanR strains
Sample: Lrp::kanR Minimal logarithmic rep2-RNAseq
SAMN08716859 • SRS3049073 • All experiments • All runs
Library:
Instrument: NextSeq 500
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: RNA was harvested using Qiagen RNAProtect. RNA was isolated, and rRNA depletion was performed according to the Illumina Ribo-Zero rRNA Removal Kit for Bacteria. Specific Lrp-DNA complexes were isolated using a monoclonal antibody developed against Lrp, and DNA was isolated by phenol-chloroform extraction. DNA was preprared for sequencing using the NEBNext DNA Library Prep Kit. RNA was prepared fro sequencing using the NEBNext Ultra Directionaly RNA Library Prep Kit.
Experiment attributes:
GEO Accession: GSM3043142
Links:
Runs: 1 run, 5.9M spots, 445.8M bases, 141.9Mb
Run# of Spots# of BasesSizePublished
SRR68411075,865,887445.8M141.9Mb2018-11-28

ID:
5231645

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