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Links from GEO DataSets

Items: 20

1.

Genome-wide mapping of DROSHA cleavage sites on primary microRNAs and novel substrates

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Other
Platform:
GPL16791
13 Samples
Download data
Series
Accession:
GSE93653
ID:
200093653
2.

Genome-wide mapping of DROSHA cleavage sites on primary microRNAs and novel substrates [fCLIP-seq]

(Submitter supplied) MicroRNA (miRNA) maturation is initiated by DROSHA, a double-stranded RNA (dsRNA)-specific RNase III enzyme. By cleaving primary miRNAs (pri-miRNAs) at specific positions, DROSHA serves as a main determinant of miRNA sequences and a highly selective gate-keeper for the canonical miRNA pathway. However, the sites of DROSHA-mediated processing have not been annotated on a genomic scale, and it remains unclear to what extent DROSHA functions outside the miRNA pathway. more...
Organism:
Homo sapiens
Type:
Other
Platform:
GPL16791
4 Samples
Download data: TSV
Series
Accession:
GSE93651
ID:
200093651
3.

Genome-wide mapping of DROSHA cleavage sites on primary microRNAs and novel substrates [RNA-seq]

(Submitter supplied) MicroRNA (miRNA) maturation is initiated by DROSHA, a double-stranded RNA (dsRNA)-specific RNase III enzyme. By cleaving primary miRNAs (pri-miRNAs) at specific positions, DROSHA serves as a main determinant of miRNA sequences and a highly selective gate-keeper for the canonical miRNA pathway. However, the sites of DROSHA-mediated processing have not been annotated on a genomic scale, and it remains unclear to what extent DROSHA functions outside the miRNA pathway. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
9 Samples
Download data: TSV
Series
Accession:
GSE93650
ID:
200093650
4.

DROSHA complementation experiments using small RNA sequencing

(Submitter supplied) DROSHA complementation experiments were performed to check whether dsRBD of DROSHA recognizes the lower stem of pri-miRNAs and affects miRNA biogenesis.
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL16791
17 Samples
Download data: TXT
Series
Accession:
GSE117603
ID:
200117603
5.

High-throughput in vitro DROSHA processing on 38,880 pri-miRNA variants

(Submitter supplied) To investigate the precise processing mechanism of pri-miRNA, we prepared 38,880 pri-miRNA variants which contain unique barcode sequences (Fang and Bartel, Mol Cell, 60: 131) and performed high-throughput processing experiments.
Organism:
synthetic construct
Type:
Other
Platform:
GPL19604
3 Samples
Download data: TXT
Series
Accession:
GSE117600
ID:
200117600
6.

The bulges control in pri-miRNA processing in the position and strand-dependent manner

(Submitter supplied) The microRNA (miRNA) biogenesis is responsible for the production of miRNAs that play critical roles in gene expression and numerous human diseases. The adequate biogenesis of miRNAs is largely determined by the efficiency and fidelity of primary microRNA (pri-miRNA) processing by Microprocessor. Here, we investigated the roles of a secondary RNA element, an RNA bulge, in pri-miRNA processing. We discovered that the 3p-strand bulges in positions 7-9 from the Microprocessor cleavage sites (midB_7-9) contributes to determining the cleavage sites of Microprocessor, the 5p- and 3p-strand bugles in positions 10-12 (midB_10-12) blocked the unproductive cleavage, and the 3p-strand bulges in positions 6-7 (seedB) inhibited the productive cleavage of Microprocessor. more...
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL18573
15 Samples
Download data: FASTA, TXT
Series
Accession:
GSE158060
ID:
200158060
7.

The high-throughput pri-miRNA cleavage assays on 262144 variants

(Submitter supplied) Microprocessor (MP), DROSHA-DGCR8, processes primary miRNA transcripts (pri-miRNAs) to initiate miRNA biogenesis. The canonical cleavage mechanism of MP has been extensively investigated and comprehensively validated for two decades. However, this canonical mechanism cannot account for the processing of certain pri-miRNAs in animals. In this study, by conducting high-throughput pri-miRNA cleavage assays for approximately 260,000 pri-miRNA sequences, we discovered and comprehensively characterized a noncanonical cleavage mechanism of MP. more...
Organism:
synthetic construct
Type:
Other
Platform:
GPL26526
8 Samples
Download data: TXT
Series
Accession:
GSE216012
ID:
200216012
8.

Small RNA sequencing of DROSHA-KO HCT116 cells transfected with DROSHA wild type and mutants

(Submitter supplied) The experiments were conducted to examine the effects of DROSHA mutations on miRNA biogenesis
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL18573
12 Samples
Download data: TXT
Series
Accession:
GSE215796
ID:
200215796
9.

HP1BP3, a chromatin retention factor for co-transcriptional microRNA processing

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL11154
10 Samples
Download data
Series
Accession:
GSE77856
ID:
200077856
10.

HP1BP3, a chromatin retention factor for co-transcriptional microRNA processing (miRNA-Seq)

(Submitter supplied) Identification and characterization of HP1BP3 (a human histone H1 homologue) as a novel chromatin retention factor essential for the co-transcriptional processing of pri-miRNA.
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL11154
4 Samples
Download data: XLS
Series
Accession:
GSE77855
ID:
200077855
11.

HP1BP3, a chromatin retention factor for co-transcriptional microRNA processing (ChIP-Seq)

(Submitter supplied) Identification and characterization of HP1BP3 (a human histone H1 homologue) as a novel chromatin retention factor essential for the co-transcriptional processing of pri-miRNA.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL11154
6 Samples
Download data: BED
Series
Accession:
GSE77854
ID:
200077854
12.

MicroRNA-seq of cell lines expressing pri-miR-9 paralog constructs

(Submitter supplied) MicroRNA (miRNA) biogenesis begins with Drosha cleavage, the fidelity of which is critical for downstream processing and mature miRNA target specificity. To understand how pri-miRNA sequence and structure influence Drosha cleavage, we studied the processing of three pri-miR-9 paralogs (pri-miR-9-1, pri-miR-9-2 and pri-miR-9-3), which encode the same miRNA but differ in the surrounding scaffold. We show that pri-miR-9-1 has a unique Drosha cleavage profile due to its kinked tertiary structure. more...
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL15520
30 Samples
Download data: TSV
13.

MicroRNA-seq of cell lines expressing pri-miR-9 paralog constructs II

(Submitter supplied) MicroRNA (miRNA) biogenesis begins with Drosha cleavage, the fidelity of which is critical for downstream processing and mature miRNA target specificity. To understand how pri-miRNA sequence and structure influence Drosha cleavage, we studied the processing of pri-miR-9-1 sequence variants, which encode the same mature miRNA but differ in the surrounding scaffold. We show that, in addition to previously known features, the overall structural flexibility of pri-miRNA impacts Drosha cleavage fidelity. more...
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL15520
6 Samples
Download data: TSV
14.

Re-evaluation of the roles of DROSHA, Exportin 5, and DICER in microRNA biogenesis

(Submitter supplied) Biogenesis of canonical microRNAs (miRNAs) involves multiple steps: nuclear processing of primary miRNA (pri-miRNA) by DROSHA, nuclear export of precursor miRNA (pre-miRNA) by Exportin 5 (XPO5), and cytoplasmic processing of pre-miRNA by DICER. To gain a deeper understanding of the contribution of each of these maturation steps, we deleted DROSHA, XPO5, and DICER in the same human cell line, and analyzed their effects on miRNA biogenesis. more...
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL15520
9 Samples
Download data: TXT
Series
Accession:
GSE77989
ID:
200077989
15.

High-throughput in vitro DROSHA processing on human pri-miRNA variants

(Submitter supplied) The in vitro high-throughput human pri-miRNA processing assays were conducted to check whether mismatches and wobble base pairs in the upper stem of pri-miRNAs affects the DROSHA cleavage.
Organism:
synthetic construct
Type:
Other
Platform:
GPL19424
6 Samples
Download data: TXT
Series
Accession:
GSE142140
ID:
200142140
16.

The effect of mismatches and wobble base pairs in the upper stem of pri-miRNAs on DROSHA cleavage using small RNA sequencing

(Submitter supplied) The experiments were conducted to check whether mismatches and wobble base pairs in the upper stem of pri-miRNAs affects the DROSHA cleavage and thereby miRNA biogenesis.
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL16791
4 Samples
Download data: TXT
Series
Accession:
GSE142136
ID:
200142136
17.

High-throughput in vitro DROSHA processing on artificial variants

(Submitter supplied) MicroRNAs (miRNAs) are small RNAs that regulate gene expression. miRNAs are produced from primary miRNAs (pri-miRNAs), the cleavage of which is catalyzed by the Microprocessor complex. Microprocessor therefore plays a key role in determining the efficiency and precision of miRNA production, and thus the function of the final miRNA product. In this study, we utilized high-throughput sequencing-integrated enzymology with purified Microprocessor proteins and randomized pri-miRNA sequences to investigate the catalytic mechanism of Microprocessor. more...
Organism:
synthetic construct
Type:
Other
Platform:
GPL26697
9 Samples
Download data: TXT
Series
Accession:
GSE131636
ID:
200131636
18.

Circadian analysis of miRNAs and their targets

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Drosophila melanogaster
Type:
Expression profiling by array; Expression profiling by genome tiling array
Platforms:
GPL1322 GPL5919
28 Samples
Download data: BAR, CEL, TXT
Series
Accession:
GSE17629
ID:
200017629
19.

Tiling arrays from control and flies without Drosha or Pasha

(Submitter supplied) Little is known about the contribution of translational control to circadian rhythms. To address this issue and in particular translational control by microRNAs (miRNAs), we knocked down the miRNA biogenesis pathway in Drosophila circadian tissues. In combination with an increase in circadian-mediated transcription, this severely affected Drosophila behavioral rhythms, indicating that miRNAs function in circadian timekeeping. more...
Organism:
Drosophila melanogaster
Type:
Expression profiling by genome tiling array
Platform:
GPL5919
1 Sample
Download data: BAR, CEL, TXT
Series
Accession:
GSE17628
ID:
200017628
20.

Genome wide identification of targets of the drosha-pasha/DGCR8 complex

(Submitter supplied) Drosha is a type III RNAse, which plays a critical role in miRNA biogenesis. Drosha and its double-stranded RNA-binding partner protein Pasha/DGCR8 likely recognize and cleave miRNA precursor RNAs or pri-miRNA hairpins co-transcriptionally. To identify RNAs processed by Drosha, we used tiling microarrays to examine transcripts after depletion of drosha mRNA with dsRNA in Drosophila Schneider S2 cells. more...
Organism:
Drosophila melanogaster
Type:
Expression profiling by genome tiling array; Genome binding/occupancy profiling by genome tiling array
Platforms:
GPL6629 GPL5919
7 Samples
Download data: BAR, CEL
Series
Accession:
GSE14215
ID:
200014215
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