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Links from GEO DataSets

Items: 20

1.

Target identification for R0199

(Submitter supplied) In this study we determined the target spectrum of C. crescentus sRNA R0199 via pulse-expression followed by RNA-sequencing.
Organism:
Caulobacter vibrioides
Type:
Expression profiling by high throughput sequencing
Platform:
GPL28356
6 Samples
Download data: XLSX
Series
Accession:
GSE148208
ID:
200148208
2.

Genome-wide profiling of Hfq-bound RNAs reveals the iron-responsive small RNA RusT in Caulobacter crescentus

(Submitter supplied) The alpha-proteobacterium Caulobacter crescentus thrives in oligotrophic environments and is able to optimally exploit minimal resources by entertaining an intricate network of gene expression control mechanisms. Numerous transcriptional activators and repressors have been reported to contribute to these processes, but only few studies have focused on regulation at the post-transcriptional level in C. more...
Organism:
Caulobacter vibrioides
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL24555
2 Samples
Download data: XLSX
Series
Accession:
GSE247928
ID:
200247928
3.

To be updated

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Caulobacter vibrioides
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL21016 GPL28356
10 Samples
Download data
Series
Accession:
GSE148211
ID:
200148211
4.

RNA co-immunoprecipitation with 3xFLAG::Hfq in Caulobacter crescentus

(Submitter supplied) In this study we used RNA co-immunoprecipitation followed by RNA-sequencing to identify Hfq-binding RNAs in C. crescentus.
Organism:
Caulobacter vibrioides
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21016
4 Samples
Download data: XLSX
Series
Accession:
GSE148206
ID:
200148206
5.

Identification of small RNAs expressed in Caulobacter crescentus in response to DNA damage

(Submitter supplied) RNA-based regulation of gene expression is substantially contributing to the ability of bacteria to rapidly adapt to changing environmental conditions. This study employs RNAseq to define the transcriptome of Caulobacter in response to treatment with the DNA-crosslinking agent mitomycin C. We identify a small, regulatory RNA ChvR synthesized under the control of the conserved ChvIG two-component system which represses production of a TonB-dependent receptor, ChvT, in Caulobacter crescentus. more...
Organism:
Caulobacter vibrioides NA1000
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21317
6 Samples
Download data: WIG
Series
Accession:
GSE104186
ID:
200104186
6.

Polynucleotide phosphorylase promotes the stability and function of Hfq-binding sRNAs by degrading target mRNA-derived fragments

(Submitter supplied) In many gram-negative and some gram-positive bacteria small regulatory RNAs (sRNAs) that bind the RNA chaperone Hfq have a pivotal role in modulating virulence, stress responses, metabolism, and biofilm formation. These sRNAs recognize transcripts through base-pairing, and sRNA-mRNA annealing consequently alters the translation and/or stability of transcripts leading to changes in gene expression. We have previously found that the highly conserved 3'-to-5' exoribonuclease polynucleotide phosphorylase (PNPase) has an indispensable role in paradoxically stabilizing Hfq-bound sRNAs and promoting their function in gene regulation in Escherichia coli. more...
Organism:
Escherichia coli str. K-12 substr. MG1655
Type:
Expression profiling by high throughput sequencing; Other
Platform:
GPL15010
12 Samples
Download data: TXT, XLSX
Series
Accession:
GSE125368
ID:
200125368
7.

Multiple in vivo roles for the C-terminal domain of the RNA chaperone Hfq

(Submitter supplied) Hfq, a bacterial RNA chaperone, stabilizes small regulatory RNAs (sRNAs) and facilitates sRNA base-pairing with target mRNAs. Hfq has a conserved N-terminal domain and a poorly conserved disordered C-terminal domain (CTD). In a transcriptome-wide examination of the effects of a chromosomal CTD deletion (Hfq1-65), the Escherichia coli mutant was most defective for the accumulation of sRNAs that bind the proximal and distal faces of Hfq (Class II sRNAs), but other sRNAs also were affected. more...
Organism:
Escherichia coli K-12
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24570
8 Samples
Download data: TXT
Series
Accession:
GSE139988
ID:
200139988
8.

Hfq CLASH uncovers sRNA-target interaction networks linked to nutrient availability adaptation

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Escherichia coli str. K-12 substr. MG1655
Type:
Expression profiling by high throughput sequencing; Other
Platforms:
GPL24659 GPL26592
30 Samples
Download data: FA, GTF
Series
Accession:
GSE123050
ID:
200123050
9.

Hfq CLASH uncovers sRNA-target interaction networks linked to nutrient availability adaptation [CLASH]

(Submitter supplied) By shaping gene expression profiles, small RNAs (sRNAs) enable bacteria to efficiently adapt to changes in their environment. To better understand how Escherichia coli acclimatizes to nutrient availability, we performed UV cross-linking, ligation and sequencing of hybrids (CLASH) to uncover Hfq-associated RNA-RNA interactions at specific growth stages. We demonstrate that Hfq CLASH robustly captures bona fide RNA-RNA interactions identified hundreds of novel sRNA base-pairing interactions, including many sRNA-sRNA interactions and involving 3’UTR-derived sRNAs. more...
Organism:
Escherichia coli str. K-12 substr. MG1655
Type:
Other
Platform:
GPL24659
16 Samples
Download data: TXT
Series
Accession:
GSE123049
ID:
200123049
10.

Hfq CLASH uncovers sRNA-target interaction networks linked to nutrient availability adaptation [RNA-seq]

(Submitter supplied) By shaping gene expression profiles, small RNAs (sRNAs) enable bacteria to efficiently adapt to changes in their environment. To better understand how Escherichia coli acclimatizes to nutrient availability, we performed UV cross-linking, ligation and sequencing of hybrids (CLASH) to uncover Hfq-associated RNA-RNA interactions at specific growth stages. We demonstrate that Hfq CLASH robustly captures bona fide RNA-RNA interactions identified hundreds of novel sRNA base-pairing interactions, including many sRNA-sRNA interactions and involving 3’UTR-derived sRNAs. more...
Organism:
Escherichia coli str. K-12 substr. MG1655
Type:
Expression profiling by high throughput sequencing
Platform:
GPL26592
14 Samples
Download data: XLSX
Series
Accession:
GSE123048
ID:
200123048
11.

Transcriptome-wide identification of Hfq-associated RNAs in Brucella suis by deep sequencing

(Submitter supplied) We report the identification of new noncoding RNAs in Brucella suis 1330 and that are associated to the chaperone protein Hfq
Organism:
Brucella suis 1330
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20974
2 Samples
Download data: GR
Series
Accession:
GSE73621
ID:
200073621
12.

Genome-wide identification of Hfq-regulated small RNAs in the bacterial pathogen Erwinia amylovora

(Submitter supplied) RNA-seq analysis was performed to examine the sRNA transcripts in wild type E. amylovora 1189 and in the deletion mutant of hfq, at 6 and 12 hours of culture in hrp-inducing minimal medium.
Organism:
Erwinia amylovora
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL18131
12 Samples
Download data: GTF, TXT
Series
Accession:
GSE53763
ID:
200053763
13.

A novel acetyltransferase regulates the RNA binding capacity of the RNA chaperone Hfq in Escherichia coli

(Submitter supplied) Bacterial small regulatory RNAs (sRNAs) regulate gene expression by base-pairing to their target mRNAs. In Escherichia coli and many other bacteria, this process is dependent on the RNA chaperone Hfq, which binds sRNAs and mRNAs on different faces. YhbS (renamed here as HqbA), a putative Gcn5-related N-acetyltransferase (GNAT), was identified as a novel silencer of sRNA signaling in a genomic library screen. more...
Organism:
Escherichia coli str. K-12 substr. MG1655
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18956
24 Samples
Download data: XLSX
Series
Accession:
GSE235194
ID:
200235194
14.

Defining the transcriptional regulon of ChvI in Caulobacter crescentus

(Submitter supplied) We sought to define the transcriptional regulon of the ChvI response regulator in Caulobacter crescentus. This study compares gene expression between ∆chvI cells and cells overexpressing the constitutively-active chvI(D52E) mutant. Our work provides a global view of the genes directly and indirectly regulated by the ChvGI two-component system in C. crescentus.
Organism:
Caulobacter vibrioides
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24555
12 Samples
Download data: TXT
Series
Accession:
GSE168965
ID:
200168965
15.

Identification of RNA molecules associated with the RNA-chaperone Hfq

(Submitter supplied) We used high-throughput methods to discover the Salmonella RNAs that are targeted by the bacterial Sm-like protein, Hfq. Our generic approach, using chromosomal epitope tagging and coIP-on-chip will also be useful to identify the post-transcriptional regulons of many other RNA-binding proteins. Keywords: coIP-chip
Organism:
Salmonella enterica; Salmonella enterica subsp. enterica serovar Typhimurium
Type:
Other
Platform:
GPL5791
4 Samples
Download data: TXT
Series
Accession:
GSE10149
ID:
200010149
16.

Effect of hfq-deletion on Salmonella transcriptome

(Submitter supplied) The expression profile of an S. Typhimurium hfq mutant-strain was compared to the parental strain under 2 different growth conditions; early stationary phase and SPI-1 (Salmonella pathogenicity island 1) inducing condition. Keywords: Genetic modification
Organism:
Salmonella enterica
Type:
Expression profiling by array
Platform:
GPL5780
12 Samples
Download data: TXT
Series
Accession:
GSE8985
ID:
200008985
17.

PhrS pulse expression RNA-seq

(Submitter supplied) A key challenge for understanding the role(s) played by short, non-coding RNAs (sRNAs) in bacteria is identifying the mRNA targets regulated by the sRNAs. Because the Hfq protein mediates the interactions between many sRNAs and the corresponding target mRNAs, one apporach to identify the mRNA targets of sRNAs is to capture sRNA:mRNA interactions occuring on Hfq by exposing cells to UV-irradiation, which forms cross-links between nucleic acids and proteins. more...
Organism:
Pseudomonas aeruginosa
Type:
Expression profiling by high throughput sequencing
Platform:
GPL33271
9 Samples
Download data: BW
Series
Accession:
GSE227772
ID:
200227772
18.

PAO1 Hfq-V RIL-seq and RNA-seq

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Pseudomonas aeruginosa; Pseudomonas aeruginosa PAO1
Type:
Expression profiling by high throughput sequencing; Other
Platforms:
GPL33271 GPL23999
33 Samples
Download data: BW
Series
Accession:
GSE216135
ID:
200216135
19.

PAO1 Hfq-V RNA-seq

(Submitter supplied) A key challenge for understanding the role(s) played by short, non-coding RNAs (sRNAs) in bacteria is identifying the mRNA targets regulated by the sRNAs. Because the Hfq protein mediates the interactions between many sRNAs and the corresponding target mRNAs, one apporach to identify the mRNA targets of sRNAs is to capture sRNA:mRNA interactions occuring on Hfq by exposing cells to UV-irradiation, which forms cross-links between nucleic acids and proteins. more...
Organism:
Pseudomonas aeruginosa PAO1
Type:
Expression profiling by high throughput sequencing
Platform:
GPL23999
12 Samples
Download data: BW
Series
Accession:
GSE216134
ID:
200216134
20.

PAO1 Hfq-V RIL-seq

(Submitter supplied) A key challenge for understanding the role(s) played by short, non-coding RNAs (sRNAs) in bacteria is identifying the mRNA targets regulated by the sRNAs. Because the Hfq protein mediates the interactions between many sRNAs and the corresponding target mRNAs, one apporach to identify the mRNA targets of sRNAs is to capture sRNA:mRNA interactions occuring on Hfq by exposing cells to UV-irradiation, which forms cross-links between nucleic acids and proteins. more...
Organism:
Pseudomonas aeruginosa PAO1
Type:
Other; Expression profiling by high throughput sequencing
Platform:
GPL23999
12 Samples
Download data: BED, BW
Series
Accession:
GSE216133
ID:
200216133
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