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SRX7711434: GSM4307177: 3xdelta-relQ-30min-ohne-AHT-f_S11_R1_001; Staphylococcus aureus; RNA-Seq
1 ILLUMINA (NextSeq 500) run: 11.9M spots, 893.8M bases, 320.9Mb downloads

Submitted by: NCBI (GEO)
Study: Increasing the cellular (pp)pGpp level is associated with activation of stress response genes in Staphylococcus aureus
show Abstracthide Abstract
The stringent response is characterized by the synthesis of the messenger molecules pppGpp, ppGpp or pGpp (collectively designated (pp)pGpp). The phenotypic consequences resulting from (pp)pGpp accumulation vary among species and can be mediated by different underlying mechanisms. Most genome-wide analyses were performed under stress conditions, which often mask the immediate effects of (pp)pGpp mediated regulatory circuits. In Staphylococcus aureus (pp)pGpp can be synthesized via the RelA-SpoT- homologue (RSHSau) upon amino-acid limitation or via one of the two small (p)ppGpp synthetases RelP or RelQ upon cell-wall stress. We used RNA-seq to compare global effects in response to transcriptional induction of the synthetase domain of RSH (RSH- Syn) or RelQ without the need to apply additional stress conditions. We found a significant upregulation of iron and oxidative stress genes. Simultanously, virulence genes psms were upregulated independ of the its regulator Agr. Based and these RNA-Seq results we created mutants of the regulators PerR, Fur and SarA which are associated with the regulation of oxidative stress and iron Overall design: We compared the trascriptional downstream effects of (pp)pGpp by transcriptional induction of RSH-Syn and RelQ by RNA Seq, triplicates, Illumina Next Seq 500 system,
Sample: 3xdelta-relQ-30min-ohne-AHT-f_S11_R1_001
SAMN14087174 • SRS6134507 • All experiments • All runs
Library:
Instrument: NextSeq 500
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: SINGLE
Construction protocol: Pellet was solved in Trizol. Strains were lysed using 0.5mm circonia silicia beads. Chloroform was used seperate RNA from DNA and proteins. RNA extraction was performed following the protocol by Amp Tech ExpressArt® RNA ready RNA was examined by a capillary electrophoresis on a Shimadzu MultiNA microchip followed by rRNA depletion using Ribo-Zero rRNA removel Kit from Illumina. RNA was converted to cDNA by fragmenting RNA samples by ultrasound and ligating an oligonucleotide adapter to the 3'end of the RNA. Using M-MLV reverse transcriptase first strand cDNA was created using 3' adapter as primer. The 5'Illumina TruSeq sequencing adapter was ligated to the 3'end of the purified (Agencourt AMPure XP kit) cDNA and PCR was performed. Samples were pooled in equimolar amounts and fractionated in a size range of 200-500 bp using a preparative agarose gel and Illumina sequencing was performed using 75bp reads.
Experiment attributes:
GEO Accession: GSM4307177
Links:
Runs: 1 run, 11.9M spots, 893.8M bases, 320.9Mb
Run# of Spots# of BasesSizePublished
SRR1107127811,916,969893.8M320.9Mb2020-09-01

ID:
10080143

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