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Links from GEO DataSets

Items: 20

1.

Expression analysis of Listeria monocytogenes LO28 delta-lhrC1-5 mutant and LO28 wt

(Submitter supplied) Investigation of whole genome gene expression level changes in Listeria monocytogenes LO28 delta-lhrC1-5 mutant, compared to the wild type strain. The lhrC1-5 genes encode the regulatory sRNAs LhrC1-5. The microarray studied the gene expression of unstressed cells and cells exposed to cefuroxime for 30 min. The lhrC1-5 mutant employed in this study is further described in Sievers et al. (2014) A multicopy sRNA of Listeria monocytogenes regulates expression of the virulence adhesin LapB. more...
Organism:
Listeria monocytogenes LO28; Listeria monocytogenes
Type:
Expression profiling by array
Platform:
GPL18538
12 Samples
Download data: PAIR
Series
Accession:
GSE68996
ID:
200068996
2.

Genome-wide transcriptional profiling of the cell envelope stress response of Listeria monocytogenes

(Submitter supplied) The Gram-positive bacterium Listeria monocytogenes is widely distributed in the environment and capable of causing food-borne infections in susceptible individuals. In this study, we investigated the cell envelope stress response in L. monocytogenes. Whole-genome transcriptional profiling was performed to investigate the response upon exposure to the cell wall antibiotic cefuroxime. Differential expression (≥ 2-fold difference) of 558 genes was observed, corresponding to 20% of the L. more...
Organism:
Listeria monocytogenes EGD-e; Listeria monocytogenes
Type:
Expression profiling by array
Platform:
GPL14687
16 Samples
Download data: TXT
Series
Accession:
GSE32913
ID:
200032913
3.

Characterize the regulon of 6C sRNA in Mycobacteria smegmatis

(Submitter supplied) Purpose: The goals of this study are to identify the putative mRNA targets that are regulated by the 6C sRNA. We constuct an inducible vector to transiently overexpressed the 6C sRNA in M. smegmatis, and then we perform RNA-Seq to look for genes that are differicently expressed upon the over-expression of 6C sRNA, which we think these genes are the potential targets of the 6C sRNA.
Organism:
Mycolicibacterium smegmatis
Type:
Expression profiling by high throughput sequencing
Platform:
GPL25523
2 Samples
Download data: TXT
Series
Accession:
GSE119364
ID:
200119364
4.

Hfq-coIP overgrowth

(Submitter supplied) The small RNAs associated with protein Hfq constitute one of the largest classes of post-transcriptional regulators known to date. Most previously investigated members of this class are encoded by conserved free-standing genes. Here, deep sequencing of Hfq-bound transcripts from multiple stages of growth of Salmonella Typhimurium revealed a plethora of new small RNA species from within mRNA loci, including DapZ which overlaps with the 3’ region of the biosynthetic gene, dapB. more...
Organism:
Salmonella enterica subsp. enterica serovar Typhimurium str. SL1344
Type:
Other
Platform:
GPL15732
14 Samples
Download data: WIG
Series
Accession:
GSE38884
ID:
200038884
5.

Targets of the small regulatory RNA DapZ

(Submitter supplied) To determine the targets of the small regulatory RNA DapZ in S. Typhimurium, we looked at the effect of a short pulse of DapZ over-expression on the Salmonella transcriptome, as well as a DapZ variant that lacks the GcvB-like R1 region. To achieve over-expression, the wild-type DapZ and its variant were cloned in the pBAD plasmid and induced with 0.2% L-arabinose for 10 min. We then extracted the total RNA for transcriptional profiling. more...
Organism:
Salmonella enterica subsp. enterica serovar Typhimurium str. SL1344
Type:
Expression profiling by array
Platform:
GPL11416
6 Samples
Download data: TXT
Series
Accession:
GSE38523
ID:
200038523
6.

RNA-sequencing based analysis of Listeria monocytogenes 10403S::ΔBCHL Prha-sigH and ΔBCHL Prha

(Submitter supplied) In this study, RNA-seq was used to compare the transcriptomes of Listeria monocytogenes 10403S::ΔBCHL Prha-sigH and ΔBCHL Prha. RNA-seq was performed on ΔBCHL Prha-sigH and ΔBCHL Prha RNA samples representing three independent biological replicates at log phase in Brain Heart Infusion (BHI) broth under rhamnose induction. Indexed and purified cDNA libraries (6 libraries including 3 replicates for 2 strains) were loaded together onto an independent flow cell without any other samples; sequencing was carried out by running Hiseq 2500 (single-end, 150-bp per read). more...
Organism:
Listeria monocytogenes 10403S
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20912
6 Samples
Download data: TXT, XLSX
Series
Accession:
GSE73008
ID:
200073008
7.

Superfolder GFP reporters validate diverse new mRNA targets of the classic porin regulator, MicF RNA

(Submitter supplied) MicF is a textbook example of a small regulatory RNA (sRNA) that acts on a trans-encoded target mRNA through imperfect base paring. The discovery of MicF as a post-transcriptional repressor of the major Escherichia coli porin OmpF established the paradigm for a meanwhile common mechanism of translational inhibition, through antisense sequestration of a ribosome binding site. However, whether MicF regulates additional genes has remained unknown for almost three decades. more...
Organism:
Salmonella enterica subsp. enterica serovar Typhimurium str. SL1344; Salmonella enterica
Type:
Expression profiling by array
Platform:
GPL5780
6 Samples
Download data: TXT
Series
Accession:
GSE35848
ID:
200035848
8.

MS2-affinity purification coupled with RNA sequencing (MAPS) revealed MicF sRNA targetome.

(Submitter supplied) In this study, we performed MAPS (MS2-affinity purification coupled with RNA sequencing) to draw the interacting map of MicF small regulatory RNA in vivo.
Organism:
Escherichia coli K-12
Type:
Other
Platform:
GPL19168
2 Samples
Download data: TXT
Series
Accession:
GSE113584
ID:
200113584
9.

The target spectrum of SdsR small RNA in Salmonella

(Submitter supplied) Enteric model bacteria such as Escherichia coli and Salmonella enterica express hundreds of small non-coding RNAs (sRNAs), targets for most of which are yet unknown. Some of these sRNAs are remarkably well-conserved, indicating that that they serve cellular functions that go beyond the necessities of a single organism. One of these “core sRNA” of largely unknown functions is the abundant ~100-nucleotide SdsR sRNA which accumulates in stationary phase after transcription by the general stress σ-factor, σS. more...
Organism:
Salmonella enterica; Salmonella enterica subsp. enterica serovar Typhimurium str. SL1344
Type:
Expression profiling by array
Platform:
GPL5780
6 Samples
Download data: TXT
Series
Accession:
GSE77157
ID:
200077157
10.

A small RNA controls expression of the chitinase ChiA in Listeria monocytogenes

(Submitter supplied) In recent years, more than 60 small RNAs (sRNAs) have been identified in the gram-positive human pathogen Listeria monocytogenes, but their putative roles and mechanisms of action remain largely unknown. The sRNA LhrA was recently shown to be a post-transcriptional regulator of a single gene, lmo0850, which encodes a small protein of unknown function. LhrA controls the translation and degradation of the lmo0850 mRNA by an antisense mechanism, and it depends on the RNA chaperone Hfq for efficient binding to its target. more...
Organism:
Listeria monocytogenes; Listeria innocua
Type:
Expression profiling by array
Platform:
GPL5029
1 Sample
Download data: GPR
Series
Accession:
GSE26818
ID:
200026818
11.

Transcriptional profile (mRNA and sRNA) of Clostridium acetobutylicum to metabolite stress, butanol and butyrate

(Submitter supplied) The transcription profile of C. acetobutylicum to two major metabolite stress, butanol and butyric acid, was comprehensively investigated at three different concentrations of each metabolite and at four different time points (15, 30, 60 and 75 min post stress). All experiments were performed in 3 parallel biological replicates and the RNA extraction was perfomed in a manner to retain the small RNAs and hence, investigate their role and expression under stress.
Organism:
Clostridium acetobutylicum
Type:
Expression profiling by high throughput sequencing; Non-coding RNA profiling by high throughput sequencing
Platform:
GPL17364
84 Samples
Download data: TXT
Series
Accession:
GSE48349
ID:
200048349
12.

Gene expression profiling of a pressure-tolerant Listeria monocytogenes Scott A ctsR deletion mutant

(Submitter supplied) Transcriptional profling of a Listeria monocytogenes under pressure comparing ctsR mutant and wild type
Organism:
Listeria monocytogenes
Type:
Expression profiling by array
Platform:
GPL6489
4 Samples
Download data
Series
Accession:
GSE22819
ID:
200022819
13.

Identification of RoxS targets

(Submitter supplied) To identify RoxS targets and do the comparison with RoxS targets identified by pulsed SILAC experiment
Organism:
Bacillus subtilis
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19910
6 Samples
Download data: TXT
Series
Accession:
GSE229415
ID:
200229415
14.

Comparison of 5' UTR structures in Listeria monocytogenes

(Submitter supplied) To understand physiological processes in vivo, it is vital to disclose the conformation of biological molecules inside living cells and correlate their structure with their function. Here, we describe a method, FUSE (5’-UTR Structure Elucidation) that was used to characterize changes in the structures of 5’-UTRs at different conditions inside the human bacterial pathogen Listeria monocytogenes. Using FUSE, we discovered a novel RNA thermoswitch and calculated the ratio of two conformations that this thermoswitch assumes at different conditions. more...
Organism:
Listeria monocytogenes EGD-e
Type:
Other
Platform:
GPL19076
10 Samples
Download data: XLSX
Series
Accession:
GSE118387
ID:
200118387
15.

Transcriptome comparison of S. pyogenes strains MGAS2221 and 2221ΔFasX following exposure to human plasma

(Submitter supplied) The fasX gene encodes a small regulatory RNA in the group A Streptococcus (GAS). To determine the FasX regulon during GAS exposure to human plasma we compared parental strain MGAS2221 with isogenic fasX mutant strain 2221ΔFasX. Gene expression was analyzed 0, 15, and 60 minutes post-plasma exposure.
Organism:
Streptococcus pyogenes
Type:
Expression profiling by array
Platform:
GPL9080
12 Samples
Download data: CEL
Series
Accession:
GSE36645
ID:
200036645
16.

Comparative transcriptomics of pathogenic and non-pathogenic Listeria species

(Submitter supplied) Listeria monocytogenes is a human, food-borne pathogen. Genomic comparisons between L. monocytogenes and Listeria innocua, a closely related non-pathogenic species, were pivotal in the identification of protein coding genes essential for virulence. However, no comprehensive comparison has focused on the non-coding genome. We used strand-specific cDNA sequencing to produce genome-wide transcription start site (TSS) maps for both organisms, and developed a publicly available integrative browser to visualize and analyze both transcriptomes in different growth conditions and genetic backgrounds. more...
Organism:
Listeria monocytogenes EGD-e; Listeria innocua Clip11262
Type:
Other
Platforms:
GPL15272 GPL15273
16 Samples
Download data: TXT
Series
Accession:
GSE36060
ID:
200036060
17.

Genomic and Proteomic Analysis of the Alkaline-Tolerance Response (AlTR) in Listeria monocytogenes 10403S

(Submitter supplied) Information regarding the Alkaline Tolerance Response (AlTR) in Listeria monocytogenes is very limited. In this study, L. monocytogenes was shown to exhibit a significant adaptive alkaline tolerance response (AlTR) following a 1-h exposure to mild alkaline (pH 9.5), which is capable of protecting cells from subsequent lethal alkali stress (pH 12.0). Treatment of adapted cells with protein synthesis inhibitor chloramphenicol has revealed that AlTR is at least partially protein-dependent. more...
Organism:
Listeria monocytogenes; Listeria monocytogenes 10403S
Type:
Expression profiling by array
Platform:
GPL5170
1 Sample
Download data: TAV
Series
Accession:
GSE7966
ID:
200007966
18.

The cell envelope stress response mediated by the LiaFSRLm three-component system of Listeria monocytogenes is controlled via the phosphatase activity of the bifunctional histidine kinase LiaSLm

(Submitter supplied) Most members of the phylum Firmicutes harbor a two-component system, LiaSR, which is involved in the response to cell envelope stress elicited most notably by inhibitors of the lipid II cycle. In all LiaSR systems studied in detail LiaSR-mediated signal transduction was shown to be negatively controlled by a membrane protein, LiaF, encoded upstream of liaSR. In this study we have analysed the LiaSR homolog of Listeria monocytogenes (LiaSRLm). more...
Organism:
Listeria monocytogenes EGD-e; Listeria monocytogenes
Type:
Expression profiling by array
Platform:
GPL10909
11 Samples
Download data: TXT
Series
Accession:
GSE24107
ID:
200024107
19.

The LysR-type transcriptional regulator VtlR/LsrB controls expression of multiple small RNA and small protein genes in Agrobacterium tumefaciens

(Submitter supplied) We investigated the role of the LysR-type transcriptional regulator VtlR/LsrB (Atu2186) from Agrobacterium tumefaciens C58 (alias A. fabrum C58), which regulates the expression of small-regulatory-RNA (sRNA) genes such as AbcR1 and the expression of genes encoding small proteins with a domain of unknown function DUF1127. For this purpose, we constructed a vtlR/lsrB deletion mutant. Total RNA was isolated from this mutant as well as from an AbcR1 deletion mutant (Wilms et al., 2011) at optical densities (OD) of 0.5 or 0.5 and 1.5, respectively. more...
Organism:
Agrobacterium fabrum str. C58
Type:
Expression profiling by high throughput sequencing
Platform:
GPL28562
9 Samples
Download data: CSV
Series
Accession:
GSE159961
ID:
200159961
20.

MS2-affinity purification coupled with RNA sequencing (MAPS) reveals S. aureus RsaA sRNA targetome

(Submitter supplied) The virulon of Staphyloccocus aureus is controlled by intricate connections between transcriptional and post-transcriptional regulators including proteins and small non coding RNAs (sRNAs). Most of the sRNAs regulate gene expression through base-pairings with mRNAs. Here, we have applied and adapted the MS2-affinity purification approach coupled to RNA sequencing (MAPS) to determine the targetome of RsaA sRNA of S. more...
Organism:
Staphylococcus aureus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19006
6 Samples
Download data: XLSX
Series
Accession:
GSE96814
ID:
200096814
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