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Links from GEO DataSets

Items: 20

1.

Human cytomegalovirus IE2 both activates and represses initiation and modulates elongation in a context-dependent manner

(Submitter supplied) Using PRO-Seq, which profiles nascent transcripts, and a recently developed DFF-ChIP approach that informs on local chromatin environment, we show that IE2 controls viral gene transcription in three distinct capacities during late HCMV infection and reveal mechanisms involving direct binding of IE2 to viral DNA. IE2 represses a subset of viral promoters by binding within the target core promoter region, blocking the assembly preinitiation complexes (PICs). more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL24676
14 Samples
Download data: BW
Series
Accession:
GSE193026
ID:
200193026
2.

Differences in RNA polymerase II complexes and their interactions with surrounding chromatin on human and cytomegalovirus genomes

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing
Platforms:
GPL24676 GPL20301
38 Samples
Download data: BW
Series
Accession:
GSE185763
ID:
200185763
3.

Differences in RNA polymerase II complexes and their interactions with surrounding chromatin on human and cytomegalovirus genomes [ChIP-seq]

(Submitter supplied) To investigate the chromatin structure surrounding human RNA polymerase II (Pol II) transcription on host and viral genomes, chromatin immunoprecipitation (ChIP) was performed following digestion of HCMV infected primary human foreskin fibroblasts (HFFs) with DNA Fragmentation Factor (DFF). DFF is a human endonuclease responsible for cleaving between nucleosomes during apoptosis. We found that utilizing DFF as the front end for ChIP-Seq in place of sonication or Micrococcal nuclease (MNase) offered new insights into the connections between active transcription and the local chromatin on the host and that these connections were completely absent on the HCMV genome.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL24676 GPL20301
25 Samples
Download data: BW
Series
Accession:
GSE185618
ID:
200185618
4.

Human cytomegalovirus IE2 drives transcription initiation from a select subset of late infection viral promoters by host RNA polymerase II

(Submitter supplied) Herpesvirus late promoters activate gene expression after viral DNA synthesis has begun. Alphaherpesviruses utilize a viral immediate-early protein to do this, whereas beta- and gammaherpesviruses primarily use a 6-member set of viral late-acting transcription factors (LTF) that are drawn to a TATT sequence in the late promoter. The betaherpesvirus, human cytomegalovirus (HCMV), produces three immediate-early 2 protein isoforms, IE2-86, IE2-60, IE2-40, in late infection, but whether they activate late viral promoters is unknown. more...
Organism:
Homo sapiens
Type:
Other
Platform:
GPL20301
22 Samples
Download data: BED, BW
Series
Accession:
GSE139114
ID:
200139114
5.

HCMV infected Human Fibroblasts UL84 IE2 ChIPSeq

(Submitter supplied) We report ChIP-seq analsyis of human fibroblasts infected with HCMV strains AD169 and TB40E. ChIP was performed at 20 hpi for IE2 and 3 dpi for IE2 and UL84.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL18573
12 Samples
Download data: WIG
Series
Accession:
GSE169634
ID:
200169634
6.

Nucleotide resolution of RNA polymerase II transcription in human cytomegalovirus

(Submitter supplied) We performed paired-end PRO-Seq and/or PRO-Cap on human foreskin fibroblasts (HFF) infected with human cytomegalovirus (HCMV) for 4 h (strain TB40/E) or 96 h (strain Towne varS). Each sample has matched uninfected controls. Towne experiments were also performed with adapters containing 4 nt of random sequence flanking both sides (8 total bases of randomness) to enable deduplication. Reads were first mapped to the human genome (hg38) (files available on GEO). more...
Organism:
Homo sapiens
Type:
Other
Platform:
GPL20301
13 Samples
Download data: BB, BW
Series
Accession:
GSE113394
ID:
200113394
7.

Cytomegalovirus Late Transcription Factor Target Sequence Diversity Orchestrates Viral Early to Late Transcription

(Submitter supplied) Herpesviruses have a group of genes earmarked for expression late in the infection. Beta- and gammaherpesviruses utilize a six-member set of viral late transcription factors to selectively activate these genes by binding to a DNA sequence signature in gene promoters. We made an unexpected discovery that differences in sequence signature configures the late gene expression program for human cytomegalovirus, a beta-herpesvirus of global public health importance. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL24676 GPL20301 GPL20795
24 Samples
Download data: BW
8.

Nucleosome maps of the human cytomegalovirus genome reveal a temporal switch in chromatin organization linked to a major IE protein

(Submitter supplied) Human CMV (hCMV) establishes lifelong infections in most of us, causing developmental defects in human embryos and life-threatening disease in immunocompromised individuals. During productive infection, the viral >230,000-bp dsDNA genome is expressed widely and in a temporal cascade. The hCMV genome does not carry histones when encapsidated but has been proposed to form nucleosomes after release into the host cell nucleus. more...
Organism:
Human betaherpesvirus 5
Type:
Genome binding/occupancy profiling by genome tiling array; Expression profiling by genome tiling array
Platform:
GPL17446
33 Samples
Download data: GFF, PAIR
Series
Accession:
GSE48875
ID:
200048875
9.

ChIP-seq targeting Myc-tagged UL34 from human fibroblasts infected with human cytomegalovirus at 48 hours post infection

(Submitter supplied) Purpose: To identify interactions of the viral DNA-binding protein, UL34, with the viral genome during lytic-phase replication. Methods: Human fibroblasts were infected with human cytomegalovirus expressing Myc-tagged UL34 in biological duplicate. At 48 hours post infection, ChIP was performed with anti-Myc tag antibody (Cell Signaling) and the resulting DNA fragments were sequenced on Illumina MiSeq. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL15520
4 Samples
Download data: TXT
Series
Accession:
GSE106211
ID:
200106211
10.

The Zinc Finger Antiviral Protein ZAP Restricts Human Cytomegalovirus and Selectively Binds and Destabilizes Viral UL4/UL5 Transcripts

(Submitter supplied) We describe the influence of the RNA binding protein ZAP (ZC3HAV1) on the CMV gene expression cascade
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Other
Platforms:
GPL20301 GPL24676 GPL18573
54 Samples
Download data: BW, NARROWPEAK, TSV
11.

ICP22 of Herpes Simplex Virus 1 decreases RNA Polymerase Processivity

(Submitter supplied) These data files consist of Illumina next seq 500 sequencing data from precision nuclear run-on and global nuclear run-on experiments conducted with human epithelial Hep2 cells that have been infected with human herpes simplex virus-1 (F) strain mutants. The results of these studies suggest that ICP22 is necessary for reducing Pol II processivity on the viral genome which results in its maintenance on the viral genome over the course of infection. more...
Organism:
Human alphaherpesvirus 1; Homo sapiens; Drosophila melanogaster
Type:
Expression profiling by high throughput sequencing
Platform:
GPL29914
32 Samples
Download data: BW
Series
Accession:
GSE169574
ID:
200169574
12.

RNAseq comparison of HSV-1 KOS vs n199 infected cells

(Submitter supplied) The abundance of HSV mRNAs was determines over 16h of infection in wt (KOS) and n199 (ICP22 mutant) infected cells. ICP22 is an immediate early gene of HSV that affects gene expression
Organism:
Homo sapiens; Human alphaherpesvirus 1
Type:
Expression profiling by high throughput sequencing
Platform:
GPL23890
12 Samples
Download data: XLSX
Series
Accession:
GSE109420
ID:
200109420
13.

Genome-wide occupancy of RNA polymerase II before and after heat shock in mouse cells

(Submitter supplied) The goal of this study was to understand changes that occur in RNA polymerase II occupancy upon heat shock using ChIP-seq in mouse cells.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL11002 GPL13112
4 Samples
Download data: BEDGRAPH
Series
Accession:
GSE66513
ID:
200066513
14.

RNA polymerase II ChIP-seq in HSV-1 and mock infected cells

(Submitter supplied) The goal of this study was to determine how RNA poymerase II (Pol II) occupancy changed in response to herpes simplex virus-1 (HSV-1) infection using ChIP-seq of Pol II. ChIP assays were performed 4 hours after cells were infected (or mock infected) with HSV-1. Because host cell Pol II transcribes the HSV-1 genome, the ChIP-seq data also reveal polymerase occupancy on the viral genome.
Organism:
Human alphaherpesvirus 1 strain KOS; Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL19845 GPL13112
3 Samples
Download data: BEDGRAPH
Series
Accession:
GSE66487
ID:
200066487
15.

HCMV epigenome and transcriptome during early lytic infection

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens; Human betaherpesvirus 5
Type:
Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing
Platforms:
GPL29977 GPL24676
25 Samples
Download data: BIGWIG
Series
Accession:
GSE171522
ID:
200171522
16.

Role of the HCMV immediate early proteins in controlling the HCMV transcriptome

(Submitter supplied) Purpose: to investigate the role of the HCMV immediate early genes in controlling the HCMV and cellular transcriptomes
Organism:
Homo sapiens; Human betaherpesvirus 5
Type:
Expression profiling by high throughput sequencing
Platform:
GPL29977
4 Samples
Download data: BIGWIG
Series
Accession:
GSE171521
ID:
200171521
17.

HCMV transcriptome during early lytic infection

(Submitter supplied) Purpose: to investigate expression of HCMV and cellular RNAs at early times post-infection in a lytic model
Organism:
Human betaherpesvirus 5; Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL29977
2 Samples
Download data: BIGWIG
Series
Accession:
GSE171520
ID:
200171520
18.

Transcriptome of MRC5 fibroblasts

(Submitter supplied) Purpose: to investigate the human transcriptome in MRC5 fibroblasts
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24676
3 Samples
Download data: BIGWIG
19.

Role of the HCMV immediate early proteins in controlling the HCMV and cellular epigenomes

(Submitter supplied) Purpose: to investigate the role of the HCMV immediate early proteins in controlling the HCMV and cellular epigneomes during lytic infectioin
Organism:
Homo sapiens; Human betaherpesvirus 5
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL29977
16 Samples
Download data: BIGWIG
Series
Accession:
GSE171518
ID:
200171518
20.

HCMV epigenome during early lytic infection

(Submitter supplied) Purpose: to investigate occupancy of Pol II and H3K27Ac on the HCMV and cellular genomes at early times post-infection in a lytic model
Organism:
Human betaherpesvirus 5; Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL29977
8 Samples
Download data: BIGWIG
Series
Accession:
GSE171512
ID:
200171512
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