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SRX3236427: GSM2801052: DMS-MaPSeq of purified cspA mRNA at 10°C, rep1; Escherichia coli str. K-12 substr. MG1655; OTHER
1 ILLUMINA (Illumina MiSeq) run: 642,018 spots, 385.2M bases, 172.7Mb downloads

Submitted by: NCBI (GEO)
Study: A stress response that monitors and regulates mRNA structure is central to cold-shock adaptation
show Abstracthide Abstract
Temperature influences the structural and functional properties of cellular components, necessitating stress responses to restore homeostasis following temperature shift. The heat shock circuitry is well understood, but that controlling the E. coli cold-shock adaptation program is not. We found that during the growth arrest phase (acclimation) that follows shift to low temperature, protein synthesis increases and ORF-wide mRNA secondary structure decreases. We identified two components of an mRNA surveillance system that enable recovery of translation during acclimation: RNase R assures appropriate mRNA degradation and the Csps dynamically adjust mRNA secondary structure to globally modulate protein expression level. Csps also remodel their own mRNAs to tune their expression to cellular need. Thus, appropriate translation is dynamically adjusted with Csp control. The universality of Csps in bacteria suggests broad utilization of this control mechanism. Overall design: Ribosome profiling, total RNA/mRNA-seq and DMS-seq data at 37°C and following cold shock in E. coli Please note that the samples with _1 and _2 (in the sample titles) represent biological replicates of the same experiments.
Sample: DMS-MaPSeq of purified cspA mRNA at 10°C, rep1
SAMN07728443 • SRS2560187 • All experiments • All runs
Library:
Instrument: Illumina MiSeq
Strategy: OTHER
Source: TRANSCRIPTOMIC
Selection: other
Layout: PAIRED
Construction protocol: Extraction was performed as described in detail previously (Li et al., 2012; Oh et al., 2011; Rouskin et al., 2014). For ribosome profiling, 200 ml of cell culture was rapidly filtered by passing through a nitrocellulose filter. Cell pellets was were rapidly collected using a pre-warmed metal table crumber, flash frozen in liquid nitrogen, and combined with frozen droplets of lysis buffer. Cells and lysis buffer were pulverized in 10 ml canisters (Retsch) pre-chilled in liquid nitrogen using Qiagen TissueLyser II. Pulverized lysate was thawed on ice and clarified by centrifugation at 4°C. Lysate containing 0.5 mg of RNA was digested for 1 h with 750 U of micrococcal nuclease (Roche) at 25°C. The ribosome-protected RNA fragments were isolated using a sucrose gradient followed by hot acid phenol extraction. mRNA fragments were size selected via gel purification, and ligated to 5' adenylated DNA oligo. After reverse transcription, the single stranded DNA was circularized, and PCR amplified (Oh et al., 2011; Li et al., 2014; Rouskin et al., 2014).
Experiment attributes:
GEO Accession: GSM2801052
Links:
Runs: 1 run, 642,018 spots, 385.2M bases, 172.7Mb
Run# of Spots# of BasesSizePublished
SRR6123774642,018385.2M172.7Mb2018-04-23

ID:
4551137

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