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Links from GEO DataSets

Items: 20

1.

RIP-seq of NAT10 interacted cellular and KSHV transcripts in iSLK-KSHV cells

(Submitter supplied) Flag-RIP-seq was performed in NAT10-Flag overexpressing iSLK-KSHV cells.
Organism:
Homo sapiens; Human gammaherpesvirus 8
Type:
Other
Platform:
GPL30065
12 Samples
Download data: TXT
Series
Accession:
GSE173889
ID:
200173889
2.

ac4C-seq of cellular and KSHV transcripts in iSLK-Puro, iSLK-KSHV (i.e. iSLK-RGB), iSLK-KSHV (WT), iSLK-KSHV (ΔNAT10) cells

(Submitter supplied) We used ac4C-seq to detedc cellular and KSHV transcripts in iSLK-Puro, iSLK-KSHV, iSLK-KSHV (WT), iSLK-KSHV (ΔNAT10) cells after after doxycycline and sodium butyrate treatment.
Organism:
Homo sapiens; Human gammaherpesvirus 8
Type:
Other
Platform:
GPL30065
24 Samples
Download data: TXT, XLS
Series
Accession:
GSE174161
ID:
200174161
3.

Lactylation of NAT10 promotes N4‐acetylcytidine modification on tRNASer-CGA-1-1 to boost oncogenic DNA virus KSHV reactivation

(Submitter supplied) N4-acetylcytidine (ac4C), a conserved but recently rediscovered RNA modification on tRNAs, rRNAs and mRNAs, is catalyzed by N-acetyltransferase 10 (NAT10). Lysine acylation is a ubiquitous protein modification that controls protein functions. Our latest study demonstrates a NAT10-dependent ac4C modification, which occurs on the polyadenylated nuclear RNA (PAN) encoded by oncogenic DNA virus Kaposi's sarcoma-associated herpesvirus (KSHV), can induce KSHV reactivation from latency and activate inflammasome. more...
Organism:
Homo sapiens
Type:
Other
Platform:
GPL24676
8 Samples
Download data: XLSX
Series
Accession:
GSE248740
ID:
200248740
4.

N -acetyltransferase 10 Regulates Alphavirus Replication via the N4-acetylcytidine (ac4C) modification of lymphocyte antigen six family member E (LY6E)

(Submitter supplied) To investigate whether NAT10 manipulates SINV replication by regulating downstream mRNAs, we established a Huh7 cell line in which NAT10 was knocked down by shRNA.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24676
12 Samples
Download data: TXT
Series
Accession:
GSE222477
ID:
200222477
5.

Kaposi’s Sarcoma-associated herpesvirus fine-tunes the temporal expression of its genes manipulating a specific host RNA quality control pathway

(Submitter supplied) Kaposi’s Sarcoma-associated herpesvirus (KSHV) transcripts are subject to degradation by at least two host-mediated nuclear RNA decay pathways, PABPN1 and PAPα/γ-mediated RNA decay (PPD) and an ARS2-dependent decay pathway. KSHV expresses the multifunctional protein ORF57, which increases viral transcripts stability by protecting them preferentially from ARS2-dependent decay. However, a subset of viral transcripts succumb to PPD even in the presence of ORF57, but the role of PPD during KSHV infection is not completely understood. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
12 Samples
Download data: CSV
6.

Acetylation of cytidines by NAT10 enhances HIV-1 replication through stabilization of viral RNA

(Submitter supplied) As obligate parasites, viruses need to navigate a variety of cellular regulatory systems while infecting and replicating in the host cell. Post-transcriptional modifications have recently emerged as an important layer of regulation of viral RNA function. For example, our lab and others have shown that the RNA modification N6-methyladenosine (m6A) can enhance the replication of multiple viruses in cis, including Human Immunodeficiency virus 1 (HIV-1), Influenza A virus, SV40 and Kaposi's sarcoma-associated herpesvirus (KSHV). more...
Organism:
Homo sapiens
Type:
Other
Platforms:
GPL24676 GPL20301 GPL18573
12 Samples
Download data: BED
Series
Accession:
GSE142490
ID:
200142490
7.

Chromatin association sites of KSHV and RRV PAN RNA

(Submitter supplied) During lytic replication of Kaposi’s sarcoma-associated herpesvirus (KSHV), a nuclear viral long noncoding RNA known as PAN RNA becomes the most abundant polyadenylated transcript in the cell. Knockout or knockdown of KSHV PAN RNA results in loss of late lytic viral gene expression and, consequently, reduction of progeny virion release from the cell. We studied KSHV and RRV PAN RNA homologs using capture hybridization analysis of RNA targets (CHART) and observed their reproducible associations with host chromatin, but the loci differ between PAN RNA homologs. 
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL16791 GPL11154
68 Samples
Download data: BROADPEAK
Series
Accession:
GSE121268
ID:
200121268
8.

Identification of NAT10 targets in CRC by RNA immunoprecipitation and acethyl-RNA immunoprecipitation

(Submitter supplied) To identify potential mRNAs that are acetylated by NAT10, RIP with a NAT10 antibody and acRIP with a ac4C antibody were conducted in DLD-1 and SW480 cells
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Other
Platform:
GPL24676
6 Samples
Download data: TXT
Series
Accession:
GSE210385
ID:
200210385
9.

RNA-seq analysis of human colorectal cancer cells with NAT10 deficiency.

(Submitter supplied) Transcriptional analysis of DLD-1 and SW480 cells with NAT10 knockdown.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL23227
8 Samples
Download data: TXT
Series
Accession:
GSE210384
ID:
200210384
10.

Global host gene expression changes in KSHV+ PEL cells upon KSHV reactivation

(Submitter supplied) Kaposi's sarcoma-associated herpesvirus (KSHV) is a human oncogenic virus, which maintains the persistent infection of the host by intermittently reactivating from latently infected cells to produce viral progenies. Here, we performed a comprehensive time course transcriptome analysis during KSHV reactivation in KSHV+ primary effusion B-cell lymphoma cells (PEL). For this we used a recombinant PEL cell line called TRExBCBL1-3xFLAG-RTA. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
12 Samples
Download data: TXT
11.

Genome-wide mapping of RTA binding sites in KSHV+ PEL cells during KSHV reactivation.

(Submitter supplied) Chromatin immunoprecipitation coupled with high-throughput sequencing (ChIP-seq) analysis was performed during Kaposi's sarcoma-associated herpesvirus (KSHV) reactivation in KSHV+ recombinant primary effusion B-cell lymphoma cells (PEL). RTA binding sites were identified genome-wide in a recombinant PEL cell line called TRExBCBL1-3xFLAG-RTA cells at 12 hours post-induction (hpi) of RTA expression.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL18573
2 Samples
Download data: TXT
Series
Accession:
GSE123897
ID:
200123897
12.

Effect of CTCF and Rad21 knockdown on SLK cells and KSHV gene expression

(Submitter supplied) CTCF and the cohesin complex modify chromatin by binding to DNA and interacting with each other and with other cellular proteins. Both proteins regulate transcription by a variety of local effects on transcription and by long range topological effects. CTCF and cohesin also bind to herpesvirus genomes at specific sites and regulate viral transcription during latent and lytic cycles of replication. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
9 Samples
Download data: TXT
13.

Effect of CTCF and Rad21 knockdown on cell and KSHV gene expression

(Submitter supplied) CTCF and the cohesin complex modify chromatin by binding to DNA and interacting with each other and with other cellular proteins. Both proteins regulate transcription by a variety of local effects on transcription and by long range topological effects. CTCF and cohesin also bind to herpesvirus genomes at specific sites and regulate viral transcription during latent and lytic cycles of replication. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL16791
9 Samples
Download data: BW
Series
Accession:
GSE138105
ID:
200138105
14.

Acetylation of cytidine in messenger RNA

(Submitter supplied) Generation of the "epitranscriptome through post-transcriptional ribonucleoside modification embeds a layer of regulatory complexity into RNA structure and function. Here we describe N4-acetylcytidine (ac4C) as an mRNA modification that is catalyzed by the acetyltransferase NAT10. Transcriptome-wide mapping of ac4C revealed discretely acetylated regions that were enriched within coding sequences. Ablation of NAT10 reduced ac4C detection at the mapped mRNA sites and was globally associated with target mRNA down-regulation. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Other
Platforms:
GPL16791 GPL18573
41 Samples
Download data
15.

N4-acetylcytidine of Nop2 mRNA is Required to the Transition of Morula-to-Blastocyst

(Submitter supplied) N-acetyltransferase 10 (NAT10)-mediated N4-acetylcytidine (ac4C) modification is crucial for mRNA stability and translation efficiency, yet the underlying function in mammalian preimplantation embryos remains unclear.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL28457
2 Samples
Download data: TXT
Series
Accession:
GSE236943
ID:
200236943
16.

Viral and Cellular N6-methyladenosine (m6A) Epitranscriptomes in KSHV Life Cycle

(Submitter supplied) Tan et al. discovered abundant conserved N6-methyladenosine (m6A) modifications on KSHV transcripts during latent and productive infection in different cell types. They also show that m6A readers YTHDF2 and YTHDF3 mediate KSHV replication, and KSHV optimizes both phases of viral replication by reprograming cellular epitranscriptome to regulate distinct signaling pathways.
Organism:
Homo sapiens; Rattus norvegicus
Type:
Expression profiling by high throughput sequencing; Other
Platforms:
GPL11154 GPL14844
72 Samples
Download data: BEDGRAPH, FPKM_TRACKING
Series
Accession:
GSE93676
ID:
200093676
17.

Transcriptome Analysis of KSHV during de novo primary infection of human B-and endothelial-cells

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Human gammaherpesvirus 8
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17680
24 Samples
Download data: CSV
Series
Accession:
GSE62344
ID:
200062344
18.

Transcriptome Analysis of KSHV virions produced from BCBL1 and BAC36 in 293L cells

(Submitter supplied) The objective of this study was to identify the viral transcripts packaged into the virion particles produced from BCBL1 cells as well as virions from 293L cells containing BAC36 BACs
Organism:
Human gammaherpesvirus 8
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17680
3 Samples
Download data: CSV
Series
Accession:
GSE62343
ID:
200062343
19.

Transcriptome Analysis of KSHV during de novo primary infection of endothelial (TIVE) cells

(Submitter supplied) The objective of this study was to identify the viral transcripts packaged into the virion particles and the transcription profiles of the viral genome during early infection, till the virus establishes latent infection in endothelial (TIVE) cells
Organism:
Human gammaherpesvirus 8
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17680
5 Samples
Download data: CSV
Series
Accession:
GSE62342
ID:
200062342
20.

Transcriptome Analysis of KSHV during de novo primary infection of human B cells (PBMCs)

(Submitter supplied) The objective of this study was to identify the viral transcripts packaged into the virion particles and the transcription profiles of the viral genome during early infection, till the virus establishes latent infection in human PBMCs
Organism:
Human gammaherpesvirus 8
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17680
5 Samples
Download data: CSV
Series
Accession:
GSE62341
ID:
200062341
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