U.S. flag

An official website of the United States government

Format
Items per page
Sort by

Send to:

Choose Destination

Links from GEO DataSets

Items: 20

1.

Initial  host  response to mycobacterial infection is orchestrated through H3K4 methylation-mediated RNA polymerase II binding at key immune function genes [miRNA-seq]

(Submitter supplied) Massive reprogramming of the host alveolar macrophage transcriptome occurs during the initial stages of tuberculosis. In bovine tuberculosis, Mcobacterium bovis can persist and replicate within alveolar macrophages through varied mechanisms to subvert or exploit host immune responses ( REF). To determine how these transcriptional changes are regulated we performed ChIPseq analysis of H3K4 and H3K27 methylation, established histone tail markers associated with permissive and repressive chromatin states, respectively. more...
Organism:
Bos taurus
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL19172
8 Samples
Download data: TXT
Series
Accession:
GSE116733
ID:
200116733
2.

Initial host response to mycobacterial infection is orchestrated through H3K4 methylation-mediated RNA polymerase II binding at key immune function genes.

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Bos taurus
Type:
Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing; Non-coding RNA profiling by high throughput sequencing
Platforms:
GPL23295 GPL19172
30 Samples
Download data: BW, TXT
Series
Accession:
GSE116734
ID:
200116734
3.

Initial  host  response to mycobacterial infection is orchestrated through H3K4 methylation-mediated RNA polymerase II binding at key immune function genes [RNA-seq]

(Submitter supplied) Massive reprogramming of the host alveolar macrophage transcriptome occurs during the initial stages of tuberculosis. In bovine tuberculosis, Mcobacterium bovis can persist and replicate within alveolar macrophages through varied mechanisms to subvert or exploit host immune responses ( REF). To determine how these transcriptional changes are regulated we performed ChIPseq analysis of H3K4 and H3K27 methylation, established histone tail markers associated with permissive and repressive chromatin states, respectively. more...
Organism:
Bos taurus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL23295
8 Samples
Download data: TXT
Series
Accession:
GSE116732
ID:
200116732
4.

Initial  host  response to mycobacterial infection is orchestrated through H3K4 methylation-mediated RNA polymerase II binding at key immune function genes [ChIP-seq]

(Submitter supplied) Massive reprogramming of the host alveolar macrophage transcriptome occurs during the initial stages of tuberculosis. In bovine tuberculosis, Mcobacterium bovis can persist and replicate within alveolar macrophages through varied mechanisms to subvert or exploit host immune responses ( REF). To determine how these transcriptional changes are regulated we performed ChIPseq analysis of H3K4 and H3K27 methylation, established histone tail markers associated with permissive and repressive chromatin states, respectively. more...
Organism:
Bos taurus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL23295
14 Samples
Download data: BW
Series
Accession:
GSE116731
ID:
200116731
5.

RNA sequencing provides exquisite insight into the manipulation of the alveolar macrophage by tubercle bacilli

(Submitter supplied) Mycobacterium bovis, the agent of bovine tuberculosis, causes an estimated $3 billion annual losses to global agriculture due, in part, to the limitations of current diagnostics. Development of next-generation diagnostics requires a greater understanding of the interaction between the pathogen and the bovine host. Therefore, to explore the early response of the alveolar macrophage to infection, we report the first application of RNA-sequencing to define, in exquisite detail, the transcriptomes of M. more...
Organism:
Bos taurus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL15749
78 Samples
Download data: TXT, XLSX
Series
Accession:
GSE62506
ID:
200062506
6.

The bovine alveolar macrophage (bAM) DNA methylome is resilient to infection with Mycobacterium bovis

(Submitter supplied) Whole genome bisulfite sequencing (WGBS) was used to assess the effect of M. bovis infection on the bAM DNA methylome (5-methylcytosine). The methylomes of bAM infected with M. bovis (n = 8) were compared to those of non-infected control bAM (n = 8) at 24 hours post-infection (hpi). No differences in DNA methylation (CpG or non-CpG) were observed between control and infected bAM. Analysis of DNA methylation at proximal promoter regions uncovered >250 genes harbouring intermediately methylated (IM) promoters (average methylation = 33–66%). more...
Organism:
Bos taurus
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL19172
16 Samples
Download data: TXT
Series
Accession:
GSE110412
ID:
200110412
7.

RNA-seq transcriptional profiling of peripheral blood leukocytes from cattle infected with Mycobacterium bovis

(Submitter supplied) In the present study, we have analyzed the peripheral blood leukocyte (PBL) transcriptome of eight natural M. bovis-infected and eight age- and sex-matched non-infected control Holstein-Friesian animals using RNA-seq. In addition, we compared gene expression profiles generated using RNA-seq with those previously generated using the high-density Affymetrix® GeneChip® Bovine Genome Array platform from the same PBL-extracted RNA
Organism:
Bos taurus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL15750
16 Samples
Download data: TXT, XLSX
Series
Accession:
GSE60265
ID:
200060265
8.

Whole-transcriptome, high-throughput RNA sequence analysis of the bovine macrophage response to Mycobacterium bovis infection in vitro

(Submitter supplied) Background: Mycobacterium bovis, the causative agent of bovine tuberculosis, is an intracellular pathogen that can persist inside host macrophages during infection via a diverse range of mechanisms that subvert the host immune response. In the current study, we have analysed and compared the transcriptomes of M. bovis-infected monocyte-derived macrophages (MDM) purified from six Holstein-Friesian females with the transcriptomes of non-infected control MDM from the same animals over a 24 h period using strand-specific RNA sequencing (RNA-seq). more...
Organism:
Bos taurus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL15750
14 Samples
Download data: TXT, XLSX
Series
Accession:
GSE45439
ID:
200045439
9.

MicroRNA analysis of the bovine alveolar macrophage response to Mycobacterium bovis infection suggests pathogen survival is enhanced by miRNA regulation of endocytosis and lysosome trafficking

(Submitter supplied) Purpose: The goal of this RNA-seq study was to profile changes in miRNA expression in bovine alveolar macrophages isolated from Holstein-Friesian and challenged with M. bovis over a 48 hour time course. Background: Mycobacterium bovis, the causative agent of bovine tuberculosis, is a major infectious disease problem for global agriculture, resulting in losses of billions of Euros annually. The bacterium spreads via an airborne route and is taken up by alveolar macrophages in the lung. more...
Organism:
Bos taurus
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL15749
88 Samples
Download data: TXT
Series
Accession:
GSE58883
ID:
200058883
10.

Genome-wide transcriptional profiling of peripheral blood leukocytes from cattle infected with Mycobacterium bovis

(Submitter supplied) Background: Mycobacterium bovis is the causative agent of bovine tuberculosis (BTB), a pathological infection with significant economic impact. Recent studies have highlighted the role of functional genomics to better understand the molecular mechanisms governing the host immune response to M. bovis infection. Furthermore, these studies may enable the identification of novel transcriptional markers of BTB that can augment current diagnostic tests and surveillance programmes. more...
Organism:
Bos taurus
Type:
Expression profiling by array
Platform:
GPL2112
16 Samples
Download data: CEL
Series
Accession:
GSE33359
ID:
200033359
11.

Profiling microRNA expression in bovine alveolar macrophages using RNA-seq

(Submitter supplied) In this study, we determined the miRNA expression profile of bovine alveolar macrophages, using next-generation sequencing strategy. On an Illumina HiSeq 2000 machine, we sequenced 8 miRNA libraries, prepared from small RNA fractions of alveolar macrophages isolated from 8 different healthy animals (Bos taurus). From the data, the potential novel miRNAs were predicted, and the expression levels of the known miRNAs were determined. more...
Organism:
Bos taurus
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL15749
8 Samples
Download data: TXT
Series
Accession:
GSE41138
ID:
200041138
12.

Key hub and bottleneck genes differentiate the macrophage response to virulent and attenuated Mycobacterium bovis

(Submitter supplied) Mycobacterium bovis is an intracellular pathogen that causes tuberculosis in cattle. Following infection, the pathogen resides and persists inside host macrophages by subverting host immune responses via a diverse range of mechanisms. Here, a high-density bovine microarray platform was used to examine the bovine monocyte-derived macrophage transcriptome response to M. bovis infection relative to infection with the attenuated vaccine strain, M. more...
Organism:
Bos taurus
Type:
Expression profiling by array
Platform:
GPL2112
41 Samples
Download data: CEL
Series
Accession:
GSE59774
ID:
200059774
13.

Global gene expression of bovine monocyte-derived macrophages in response to in vitro challenge with Mycobacterium bovis

(Submitter supplied) Background: Mycobacterium bovis, the causative agent of bovine tuberculosis, is a major cause of mortality in global cattle populations. Macrophages are among the first cells types to encounter M. bovis following exposure and the response elicited by these cells is pivotal in determining the outcome of infection. Here, a functional genomics approach was undertaken to investigate global gene expression profiles in bovine monocyte-derived macrophages (MDM) purified from seven age-matched non-related females, in response to in vitro challenge with M. more...
Organism:
Bos taurus
Type:
Expression profiling by array
Platform:
GPL2112
49 Samples
Download data: CEL
Series
Accession:
GSE33309
ID:
200033309
14.

Comparison of antigen stimulation response in Mycobacterium bovis-infected vs. control cattle using BOTL-5 microarray

(Submitter supplied) Bovine tuberculosis (BTB) caused by Mycobacterium bovis continues to cause substantial losses to global agriculture and has significant repercussions for human health. The advent of high throughput genomics has facilitated large scale gene expression analyses that present a novel opportunity for revealing the molecular mechanisms underlying chronic mycobacterial infection. Using this approach, we have previously shown that innate immune genes in peripheral blood mononuclear cells (PBMC) from BTB-infected animals are repressed in vivo in the absence of exogenous stimulation. more...
Organism:
Bos taurus
Type:
Expression profiling by array
Platform:
GPL5751
36 Samples
Download data: GPR
Series
Accession:
GSE12835
ID:
200012835
15.

Genome-wide mapping of histone H3 lysine 4 trimethylation in Eucalyptus grandis developing xylem

(Submitter supplied) Histone modifications play an integral role in plant development, but have been poorly studied in woody plants. Investigating chromatin organization in wood-forming tissue and its role in regulating gene expression allows us to understand the mechanisms underlying cellular differentiation during xylogenesis (wood formation) and identify novel functional regions in plant genomes. However, woody tissue poses unique challenges for using high-throughput chromatin immunoprecipitation (ChIP) techniques for studying genome-wide histone modifications in vivo. more...
Organism:
Eucalyptus grandis
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL20030
5 Samples
Download data: BEDGRAPH
Series
Accession:
GSE67873
ID:
200067873
16.

Transcriptional response of bovine moncocyte-derived macrophages to infection with strains of Mycobacterium bovis and Mycobacterium avium subspecies paratuberculosis

(Submitter supplied) Mycobacterium bovis (M. bovis) and Mycobacterium avium subspecies paratuberculosis (MAP) are important pathogens of cattle, causing bovine tuberculosis and Johne’s disease respectively. M. bovis and MAP infect residential macrophages in the lung and intestines respectively and subvert the macrophage biology to create a survival niche. To investigate this interaction we simultaneously studied the transcriptional response of bovine monocyte-derived macrophages to infection with two strains of M. more...
Organism:
Bos taurus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11153
80 Samples
Download data: TXT
Series
Accession:
GSE104211
ID:
200104211
17.

Comparative gene expression profiling analysis of RNA-seq data for bovine macrophages infected with two Myocbacterium bovis strains of variable virulence and co-cultured with autologous lymphocytes.

(Submitter supplied) In this study we compared the transcriptome of bovine macrophages infected with two Mycobacterium bovis strains of variable virulence, co-cultured with autologous lymphocytes. We used the highly virulent M. bovis strain called Mb04-303 and the attenuated Mb534 strain. We first observed that only the infection of bovine macrophages with the virulent strain, Mb04-303, induced in peripheral bovine mononuclear cells a powerful innate immune response capable of controlling the intracellular mycobacterial replication.By RNAseq analysis we found that infections with Mb04-303 downregulated the KEAP1-NFE2L2 pathway that encodes a transcriptional factor involved in antioxidant genes and inflammasome activation and upregulated the type 1 interferon signalling pathway, compared to the infections with the attenuated Mb534 strain. more...
Organism:
Bos taurus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL23055
6 Samples
Download data: CSV
Series
Accession:
GSE241059
ID:
200241059
18.

Analysis of the bovine monocyte-derived macrophage response to Mycobacterium avium subspecies paratuberculosis infection using RNA-seq

(Submitter supplied) Johne's disease, caused by infection with Mycobacterium avium subsp. paratuberculosis, (MAP), is a chronic intestinal disease of ruminants with serious economic consequences for cattle production in the United States and elsewhere. During infection, MAP bacilli are phagocytosed and subvert host macrophage processes, resulting in subclinical infections that can lead to immunopathology and dissemination of disease. more...
Organism:
Bos taurus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL15749
35 Samples
Download data: TXT, XLSX
Series
Accession:
GSE62048
ID:
200062048
19.

Dynamic transcriptional control of macrophage miRNA signature via inflammation responsive enhancers revealed using a combination of next generation sequencing-based approaches

(Submitter supplied) MicroRNAs are important components of the post-transcriptional fine-tuning of macrophage gene expression in physiological and pathological conditions. However, the mechanistic underpinnings and the cis-acting genomic factors of how macrophage polarizing signals induce miRNA expression changes are not well characterized. Therefore, we systematically evaluated the transcriptional basis underlying the inflammation-mediated regulation of macrophage microRNome using the combination of different next generation sequencing datasets. more...
Organism:
Mus musculus
Type:
Non-coding RNA profiling by high throughput sequencing; Other
Platform:
GPL17021
8 Samples
Download data: BEDGRAPH, TSV
Series
Accession:
GSE107095
ID:
200107095
20.

Expression and ChIP-seq analysis LPS stimulated THP-1 cells

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL9052 GPL5175
26 Samples
Download data: BED, CEL
Series
Accession:
GSE32325
ID:
200032325
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

db=gds|term=|query=5|qty=5|blobid=MCID_672d640a5614fa63672e78ec|ismultiple=true|min_list=5|max_list=20|def_tree=20|def_list=|def_view=|url=/Taxonomy/backend/subset.cgi?|trace_url=/stat?
   Taxonomic Groups  [List]
Tree placeholder
    Top Organisms  [Tree]

Find related data

Recent activity

Support Center