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Links from GEO DataSets

Items: 20

1.

5-methylcytosine modification and the ALYREF reader protein promote retrovirus replication

(Submitter supplied) The 5-methylcytosine (m5C) modification is present at appreciable amounts in the mammalian transcriptome, but its precise location and function is still poorly understood. Here, we identify high m5C levels and map their locations in a model retrovirus, the murine leukemia virus, and show that the ALYREF m5C reader protein regulates viral replication. Our results reveal a single-nucleotide m5C profile in a virus and its function in a eukaryotic mRNA.
Organism:
Mus musculus; Murine leukemia virus
Type:
Other
Platforms:
GPL27704 GPL27705
4 Samples
Download data: TXT
Series
Accession:
GSE139606
ID:
200139606
2.

Mapping of m6A and m5C on MLV with PA-antibody-seq

(Submitter supplied) While it has been known for several years that viral RNAs are subject to the addition of several distinct covalent modifications to individual nucleotides, collectively referred to as epitranscriptomic modifications, the effect of these editing events on viral gene expression has been controversial. Here, we report the purification of murine leukemia virus (MLV) genomic RNA to homogeneity and show that this viral RNA contains levels of N6-methyladenosine (m6A), 5-methylcytosine (m5C) and 2’O-methylated (Nm) ribonucleotides that are an order of magnitude higher than detected on bulk cellular mRNAs. more...
Organism:
Moloney murine leukemia virus
Type:
Other
Platform:
GPL26390
9 Samples
Download data: BED
Series
Accession:
GSE129302
ID:
200129302
3.

5-methylcytosine promotes mRNA export

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens; Mus musculus
Type:
Expression profiling by high throughput sequencing; Methylation profiling by high throughput sequencing
4 related Platforms
44 Samples
Download data
Series
Accession:
GSE93751
ID:
200093751
4.

Transcriptomics of siCTRL, siNSUN2 and ALYREF-RIP HeLa cells, and multiple mouse tissues

(Submitter supplied) RNA was isolated from siCTRL, siNSUN2 and ALYREF-RIP HeLa cells, and multiple mouse tissues using the TRIzol (Invitrogen) reagent by following the company manual. Approximately 2.5 µg of total RNA was then used for library preparation using a TruSeq™ RNA Sample Prep Kit v2 (Illumina, San Diego, CA, USA) according to the manufacturer’s protocol.The libraries were sequenced using HiSeq3000 (Illumina) or HiSeq2500 in paired-read mode, creating reads with a length of 101 or 125 bp. more...
Organism:
Homo sapiens; Mus musculus
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL16791 GPL21493 GPL21290
22 Samples
Download data: XLS
Series
Accession:
GSE93750
ID:
200093750
5.

Single-base resolution methylome of 5-Methylcytosine in human and mouse transcriptome

(Submitter supplied) mRNAs of siCTRL, siNSUN2 and ALYREF-RIP HeLa cells, and multiple mouse tissues were purified using oligo (dT)-conjugated magnetic beads followed by RiboMinus treatement. mRNAs were fragmented to ~200 nt and treated by Sodium bisulfite solution (pH 5.1) containing Hydroquinone. Bisulfite treated mRNAs were reverse transcribed to cDNA using ACT random hexamer primers. The cDNAs were subjected to libraries construction using KAPA Stranded mRNA-Seq Kit (KAPA) and performed sequencing on HiSeq2500 (Illumina) in pair-end mode, creating reads with a length of 125 bp. more...
Organism:
Mus musculus; Homo sapiens
Type:
Methylation profiling by high throughput sequencing
Platforms:
GPL17021 GPL16791
22 Samples
Download data: XLS
Series
Accession:
GSE93749
ID:
200093749
6.

Mapping of m6A and m5C on HIV with PA-antibody-seq

(Submitter supplied) In this GEO submission we include the PA-m6A-seq and PA-m5C-seq datasets for HIV in CEM & 293T cells
Organism:
Human immunodeficiency virus
Type:
Expression profiling by high throughput sequencing; Other
Platform:
GPL26648
11 Samples
Download data: BED
Series
Accession:
GSE130972
ID:
200130972
7.

5-methylcytosine (m5C) RNA modification controls the innate immune response to virus infection by regulating type I interferons

(Submitter supplied) Cytosine-5 methylation (m5C) is one of the most prevalent modifications of RNA, playing important roles in RNA metabolism, nuclear export, and translation. However, the potential role of RNA m5C methylation in innate immunity remains elusive. Here we show that depletion of NSUN2, an m5C methyltransferase, significantly inhibits the replication and gene expression of a wide range of RNA and DNA viruses. more...
Organism:
Homo sapiens
Type:
Other
Platform:
GPL24676
44 Samples
Download data: XLSX
Series
Accession:
GSE174374
ID:
200174374
8.

Epitranscriptomic maps of 5-methylcytosine reveal substrate diversity of NSUN methyltransferases and links to mRNA translation and turnover

(Submitter supplied) Multiple epitranscriptomic maps of the RNA modification 5-methylcytosine (m5C) have been prepared, often diverging markedly from each other in terms of site abundance and identity. Differences in detection methods, data depth and analysis pipelines, but also biological factors underly much of this disparity. To address this, we re-analysed available datasets from five human cell lines and seven tissues, generated by the prevailing bisulfite RNA sequencing method, with a coherent m5C site calling pipeline. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24676
12 Samples
Download data: TXT
Series
Accession:
GSE252369
ID:
200252369
9.

Comparative analysis of cellular mRNA incorporation into MLV and HIV1 virus-like particles

(Submitter supplied) We hypothesize that cellular mRNAs are incorporated nonselectively into retrovirus particles Keywords: comparative expression profiling
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
4 Samples
Download data: CEL, EXP
Series
Accession:
GSE7213
ID:
200007213
10.

m5C Promotes Pathogenesis of the Bladder Cancer Through Stabilizing mRNAs

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Methylation profiling by high throughput sequencing; Other
Platform:
GPL20795
145 Samples
Download data: TXT
Series
Accession:
GSE133671
ID:
200133671
11.

RNA-BisSeq for YBX1 RIP in normal T24 cell

(Submitter supplied) Flag-YBX1 overexpressed T24 cells pellets were resuspended with 2 volume of lysis buffer (150 mM KCl, 10 mM HEPES pH 7.6, 2 mM EDTA, 0.5% NP-40, 0.5 mM DTT, 1:100 protease inhibitor cocktail, 400 U/ml RNase inhibitor), and incubated at 4 °C for 30 min with rotation. Then the lysate was centrifuged at 15 000 g for 20 min. Before incubating the lysate with Flag beads, 100ul were taken as input. The anti-Flag M2 magnetic beads (Sigma, 10 μl per mg lysate) were washed with NT2 buffer (200 mM NaCl, 50 mM HEPES pH 7.6, 2 mM EDTA, 0.05% NP-40, 0.5 mM DTT, 200 U/ml RNase inhibitor) four times. more...
Organism:
Homo sapiens
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL20795
3 Samples
Download data: TXT
Series
Accession:
GSE133625
ID:
200133625
12.

Transcriptomics analysis of gene expression in human urothelial carcinoma of the bladder (UCB) and adjacent normal tissues.

(Submitter supplied) 36 cases of UCB and 29 adjacent normal bladder tissues (22 pairs) were derived from patients diagnosed with UCB and received radial cystectomy at Sun Yat-sen University Cancer Center (SYSUCC, Guangzhou, China). Total RNA was isolated using TRIzol® Reagent (Ambion). The RNA concentration and quality were determined with NanoDrop, Qubit and agarose gel analysis. The Dynabeads® mRNA Purification Kit (Ambion) was used to enrich the mRNAs, which were used as templates for RNA-Seq library construction. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20795
65 Samples
Download data: TXT
Series
Accession:
GSE133624
ID:
200133624
13.

RNA m5C analysis in wildtype and NSUN2 knockdown T24 cell

(Submitter supplied) RNA fragmentation and bisulfite conversion were performed. In brief, 200 ng of mRNAs along with 1 ng in vitro transcribed mouse dihydrofolate reductase (Dhfr) spike-in RNA were used. The bisulfite treated samples were desalted with Nanoseq with 3K omega 500/pk centrifugal devices (PALL). Sequencing was performed on an Illumina HiSeq X-Ten sequencing system. The m5C sites were called using meRanCall from meRanTK (FDR < 0.01). more...
Organism:
Homo sapiens
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL20795
2 Samples
Download data: TXT
Series
Accession:
GSE133623
ID:
200133623
14.

RNA m5C analysis in human urothelial carcinoma of the bladder (UCB) and adjacent normal tissues.

(Submitter supplied) 36 cases of UCB and 29 adjacent normal bladder tissues (22 pairs) were derived from patients diagnosed with UCB and received radial cystectomy at Sun Yat-sen University Cancer Center (SYSUCC, Guangzhou, China).Total RNA was isolated using TRIzol® Reagent (Ambion). The RNA concentration and quality were determined with NanoDrop, Qubit and agarose gel analysis. The Dynabeads® mRNA Purification Kit (Ambion) was used to enrich the mRNAs, which were used as templates for RNA-BisSeq library construction. more...
Organism:
Homo sapiens
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL20795
65 Samples
Download data: TXT
Series
Accession:
GSE133622
ID:
200133622
15.

Transcriptomics analysis of gene expression in wildtype and NSUN2 knockdown T24 cell

(Submitter supplied) Total RNA was isolated using TRIzol® Reagent (Ambion). The RNA concentration and quality were determined with NanoDrop, Qubit and agarose gel analysis. The Dynabeads® mRNA Purification Kit (Ambion) was used to enrich the mRNAs, which were used as templates for RNA-Seq library construction. RNA-Seq libraries was directly constructed by using KAPA mRNA Stranded mRNA-Seq Kit (KAPA) according to the manufacturer’s instructions. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20795
4 Samples
Download data: TXT
Series
Accession:
GSE133621
ID:
200133621
16.

PARCLIP analysis of YBX1, ELAVL1 and ALYREF to detect their binding targets

(Submitter supplied) The PAR-CLIP sample was separated by SDS-PAGE, RNA were recovered from the gel by D-tubeTM Dialyzer Midi(Millipore).The mixture were digested by 4 μg/μl proteinase K (Roche, 03115828001) and precipitated in ethanol with the help of glycogen (Thermo, R0551). RNAs in ethanol were used for the small RNA library construction (NEB, E7300L). Finally, the library was sequenced on the Illumina HiSeq X-Ten platform with paired-end 150 bp (PE150) kits. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL20795
6 Samples
Download data: TXT
Series
Accession:
GSE133620
ID:
200133620
17.

Conservation of m5C in tRNAs in the kingdom Plantae

(Submitter supplied) Here we use bisulfite conversion of RNA combined with high-throughput IIlumina sequencing (RBS-seq) to identify single-nucleotide resolution of m5C sites in transfer RNAs of all three sub-cellular transcriptomes across six diverse species that include, the single-celled algae Nannochloropsis oculata, the macro algae Caulerpa taxifolia and multi-cellular higher plants Arabidopsis thaliana, Brassica rapa, Triticum durum and Ginkgo biloba.
Organism:
Brassica rapa; Caulerpa taxifolia; Nannochloropsis oculata; Ginkgo biloba; Arabidopsis thaliana; Triticum turgidum subsp. durum
Type:
Other; Non-coding RNA profiling by high throughput sequencing
6 related Platforms
14 Samples
Download data: XLS, XLSX
Series
Accession:
GSE68448
ID:
200068448
18.

Conservation of m5C in rRNA in the kingdom Plantae

(Submitter supplied) Here we use bisulfite conversion of RNA combined with high-throughput IIlumina sequencing (RBS-seq) to identify single-nucleotide resolution of m5C sites in non-coding ribosomal RNAs of all three sub-cellular transcriptomes across six diverse species that included, the single-celled algae Nannochloropsis oculata, the macro algae Caulerpa taxifolia and multi-cellular higher plants Arabidopsis thaliana, Brassica rapa, Triticum durum and Ginkgo biloba. more...
Organism:
Ginkgo biloba; Nannochloropsis oculata; Triticum turgidum subsp. durum; Caulerpa taxifolia; Arabidopsis thaliana; Brassica rapa
Type:
Other; Non-coding RNA profiling by high throughput sequencing
6 related Platforms
13 Samples
Download data: XLSX
Series
Accession:
GSE68447
ID:
200068447
19.

tRNA 5-methylcytosine in Arabidopsis thaliana

(Submitter supplied) Here we use bisulfite conversion of RNA combined with high-throughput IIlumina sequencing (RBS-seq) to identify single-nucleotide resolution of m5C sites in transfer RNAs of all three sub-cellular transcriptomes of Arabidopsis thaliana. 5-methylcytosine sites in tRNAs were also determined in Arabidopsis T-DNA knockouts for the RNA methyltransferases TRM4A, TRM4B, TRDMT1, NSUN5 and NOP2A.
Organism:
Arabidopsis thaliana
Type:
Other; Non-coding RNA profiling by high throughput sequencing
Platform:
GPL17970
11 Samples
Download data: XLS, XLSX
Series
Accession:
GSE68445
ID:
200068445
20.

rRNA 5-methylcytosine in Arabidopsis thaliana

(Submitter supplied) Here we use bisulfite conversion of RNA combined with high-throughput IIlumina sequencing (RBS-seq) to identify single-nucleotide resolution of m5C sites in ribosomal RNAs of all three sub-cellular transcriptomes in Arabidopsis thaliana. m5C sites in rRNAs were also anlyzed in Arabidopsis T-DNA knockouts for the RNA methyltransferases TRM4A, TRM4B, TRDMT1, NSUN5, NOP2A, NOP2B and NOP2C.
Organism:
Arabidopsis thaliana
Type:
Non-coding RNA profiling by high throughput sequencing; Other
Platform:
GPL17970
25 Samples
Download data: XLS, XLSX
Series
Accession:
GSE68444
ID:
200068444
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