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Links from GEO DataSets

Items: 20

1.

GLD-1 mRNA regulation

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Caenorhabditis elegans
Type:
Genome binding/occupancy profiling by genome tiling array; Expression profiling by genome tiling array
Platform:
GPL5634
37 Samples
Download data: CEL
Series
Accession:
GSE33084
ID:
200033084
2.

mRNA expression analysis in mock and cgh-1(RNAi) animals

(Submitter supplied) To determine mRNA expression levels in mock and cgh-1(RNAi) animals, RNA was purified from young adult worms, using Trizol.
Organism:
Caenorhabditis elegans
Type:
Expression profiling by genome tiling array
Platform:
GPL5634
6 Samples
Download data: CEL, TAB, TXT
Series
Accession:
GSE36713
ID:
200036713
3.

Polysome profiling of wild-type and gld-1 mutant animals

(Submitter supplied) To determine the translational status of mRNAs in wild-type and gld-1 mutant animals, we analyzed total and polysomal RNA levels in both strains by tiling arrays
Organism:
Caenorhabditis elegans
Type:
Expression profiling by genome tiling array
Platform:
GPL5634
16 Samples
Download data: CEL, TAB, TXT
Series
Accession:
GSE33083
ID:
200033083
4.

mRNA expression analysis in wild-type, gld-1 and cgh-1 mutant animals

(Submitter supplied) To determine mRNA expression levels in wild-type, gld-1 (q485) mutant and cgh-1(tn691) mutant animals, RNA was purified from dissected gonads of young adult worms, using the PicoPur Kit.
Organism:
Caenorhabditis elegans
Type:
Expression profiling by genome tiling array
Platform:
GPL5634
9 Samples
Download data: CEL, TAB, TXT
Series
Accession:
GSE33082
ID:
200033082
5.

Identification of GLD-1 target mRNAs

(Submitter supplied) To determine which mRNAs are bound by GLD-1 we performed GLD-1 and MYC (as a negative control) immunoprecipitation experiments on wildtype animals.
Organism:
Caenorhabditis elegans
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL5634
6 Samples
Download data: CEL, TAB, TXT
Series
Accession:
GSE33081
ID:
200033081
6.

Global characterization of the oocyte-to-embryo transition in C. elegans uncovers a novel mRNA turnover mechanism

(Submitter supplied) The oocyte-to-embryo transition (OET) is thought to be mainly driven by post-transcriptional gene regulation. However, expression of both RNAs and proteins during the OET has not been comprehensively assayed. Furthermore, specific molecular mechanisms that regulate gene expression during OET are largely unknown. Here, we quantify and analyze, transcriptome-wide, expression of mRNAs, small RNAs and thousands of proteins in C. more...
Organism:
Caenorhabditis elegans
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL13657 GPL13776
8 Samples
Download data: TXT
Series
Accession:
GSE58141
ID:
200058141
7.

LIN-41 and OMA ribonucleoprotein complexes mediate a translational repression-to-activation switch controlling oocyte meiotic maturation and the oocyte-to-embryo transition in Caenorhabditis elegans

(Submitter supplied) An extended meiotic prophase is a hallmark of oogenesis. Hormonal signaling activates the CDK1/cyclin B kinase to promote oocyte meiotic maturation, which involves nuclear and cytoplasmic events. Nuclear maturation encompasses nuclear envelope breakdown, meiotic spindle assembly, and chromosome segregation. Cytoplasmic maturation involves major changes in oocyte protein translation and cytoplasmic organelles and is poorly understood. more...
Organism:
Caenorhabditis elegans
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18245
8 Samples
Download data: BIGWIG, XLSX
Series
Accession:
GSE98130
ID:
200098130
8.

Translation State Array Assay for C elegans IFE-1-dependent mRNAs

(Submitter supplied) Relative polysomal loading changes for wild type (N2) versus ife-1(bn127) C. elegans strains Strain ife-1(bn127) is null for the gene encoding one of five eIF4E isoforms in the worm, IFE-1. Only this isoform associates with P granules.
Organism:
Caenorhabditis elegans
Type:
Expression profiling by array
Platform:
GPL200
12 Samples
Download data: CEL, XLS, XLSX
Series
Accession:
GSE74459
ID:
200074459
9.

The cytoplasmic poly(A) polymerases GLD-2 and GLD-4 promote general gene expression via distinct mechanisms

(Submitter supplied) Comparision of mRNA abundance and translation efficiency mediated by cytoplasmic poly(A) polymerases in C. elegans
Organism:
Caenorhabditis elegans
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13657
27 Samples
Download data: TXT
Series
Accession:
GSE58918
ID:
200058918
10.

RIP-chip analysis of the C. elegans GLD-2 and RNP-8 protein

(Submitter supplied) C. elegans GLD-2 forms an active PAP with multiple RNA-binding partners to regulate diverse aspects of germline and early embryonic development. One GLD-2 partner, RNP-8, was previously shown to influence oocyte fate specification. To identify transcripts selectively associated with both GLD-2 and RNP-8, we employ a genomic approach using the method of RNA immunoprecipitation followed by microarray analysis (RIP-chip). more...
Organism:
Caenorhabditis elegans
Type:
Other
Platform:
GPL200
21 Samples
Download data: CEL
Series
Accession:
GSE23843
ID:
200023843
11.

Comparison of transcriptomes of N2 and fog-2(q71) mutant Caenorhabditis elegans

(Submitter supplied) In this experiment, steady-state mRNA levels were determined for replicated samples of N2 (wild-type reference) and fog-2(q71) homozygous mutant C. elegans. All samples were adult XX animals, which for N2 are self-fertile hermaphrodites and for fog-2(q71) spermless hermaphrodites, i.e. true females. For the fog-2 mutant animals, only those that had mated with males, and were thus gravid, were picked for RNA isolation. more...
Organism:
Caenorhabditis elegans
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13657
12 Samples
Download data: XLSX
Series
Accession:
GSE110998
ID:
200110998
12.

RNA immunoprecipitation of GLD-1 followed by microarray analysis of the co-IP'ed mRNAs

(Submitter supplied) RNA-binding proteins (RBPs) are critical regulators of gene expression and elucidating the interactions of RBPs with their RNA targets is necessary to understand how combinations of RBPs control transcriptome expression. The Quaking-related (QR) sub-family of STAR domain RBPs includes developmental regulators and tumor suppressors such as C. elegans GLD-1, which functions as a master regulator of germ line development. more...
Organism:
Caenorhabditis elegans
Type:
Other; Expression profiling by array
Platform:
GPL200
15 Samples
Download data: CEL
Series
Accession:
GSE21591
ID:
200021591
13.

Recruitment of mRNAs to P granules by gelation with intrinsically-disordered proteins

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Caenorhabditis elegans
Type:
Other; Expression profiling by high throughput sequencing
Platform:
GPL18245
24 Samples
Download data
Series
Accession:
GSE139881
ID:
200139881
14.

Recruitment of mRNAs to P granules by gelation with intrinsically-disordered proteins (RNAseq and ribosome profiling)

(Submitter supplied) RNA granules are cellular condensates that contain RNAs and proteins. The mechanism that drive the recruitment of many mRNAs to RNA granules are not fully understood. Here we characterize the assembly and transcriptome of the germ (P) granules of C. elegans. We find that mRNAs are recruited into P granules by condensation with the intrinsically-disordered protein MEG-3. MEG-3 binds ~500 mRNAs in C. more...
Organism:
Caenorhabditis elegans
Type:
Expression profiling by high throughput sequencing; Other
Platform:
GPL18245
12 Samples
Download data: XLSX
Series
Accession:
GSE139880
ID:
200139880
15.

Recruitment of mRNAs to P granules by gelation with intrinsically-disordered proteins (RNAseq datasets)

(Submitter supplied) RNA granules are cellular condensates that contain RNAs and proteins. The mechanism that drive the recruitment of many mRNAs to RNA granules are not fully understood. Here we characterize the assembly and transcriptome of the germ (P) granules of C. elegans. We find that mRNAs are recruited into P granules by condensation with the intrinsically-disordered protein MEG-3. MEG-3 binds ~500 mRNAs in C. more...
Organism:
Caenorhabditis elegans
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18245
6 Samples
Download data: DIFF
Series
Accession:
GSE139879
ID:
200139879
16.

Recruitment of mRNAs to P granules by gelation with intrinsically-disordered proteins (iCLIP results)

(Submitter supplied) RNA granules are cellular condensates that contain RNAs and proteins. The mechanism that drive the recruitment of many mRNAs to RNA granules are not fully understood. Here we characterize the assembly and transcriptome of the germ (P) granules of C. elegans. We find that mRNAs are recruited into P granules by condensation with the intrinsically-disordered protein MEG-3. MEG-3 binds ~500 mRNAs in C. more...
Organism:
Caenorhabditis elegans
Type:
Other
Platform:
GPL18245
6 Samples
Download data: CSV
Series
Accession:
GSE139878
ID:
200139878
17.

Chromatin reprogramming in primordial germ cells requires Nanos-dependent down-regulation of the synMuvB transcription factor LIN-15B

(Submitter supplied) The Nanos family of RNA-binding proteins has been implicated in the specification of primordial germ cells (PGCs) in a wide range of metazoans, but the underlying mechanisms remain poorly understood. We have profiled the transcriptome of PGCs lacking the nanos homologues nos-1 and nos-2 in C. elegans using cell sorting and RNA-seq. nos-1nos-2 PGCs fail to silence hundreds of genes normally expressed in oocytes and somatic cells, a phenotype reminiscent of PGCs lacking the repressive PRC2 complex. more...
Organism:
Caenorhabditis elegans
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18245
32 Samples
Download data: DIFF
Series
Accession:
GSE100652
ID:
200100652
18.

Stage-specific combinations of opposing poly(A) modifying enzymes guide gene expression during early oogenesis

(Submitter supplied) Comparision of mRNA abundance in C. elegans polyA polymerase (cytoPAP) and deadenylase (DeAd) mutants.
Organism:
Caenorhabditis elegans
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19757
15 Samples
Download data: TXT
Series
Accession:
GSE130685
ID:
200130685
19.

Specialized germline P-bodies are required to specify germ cell fate in C. elegans embryos

(Submitter supplied) In animals with germ plasm, specification of the germline involves “germ granules”, cytoplasmic condensates that enrich maternal transcripts in the germline founder cells. In C. elegans embryos, P granules enrich maternal transcripts, but surprisingly P granules are not essential for germ cell fate specification. Here we describe a second condensate in the C. elegans germ plasm. Like canonical P-bodies found in somatic cells, “germline P-bodies” contain regulators of mRNA decapping and deadenylation and, in addition, the intrinsically-disordered proteins MEG-1 and MEG-2 and the TIS11-family RNA-binding protein POS-1. more...
Organism:
Caenorhabditis elegans
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18245
4 Samples
Download data: TXT
Series
Accession:
GSE211555
ID:
200211555
20.

Identification of proteins and miRNAs that specifically bind an mRNA in vivo

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Caenorhabditis elegans
Type:
Expression profiling by high throughput sequencing; Non-coding RNA profiling by high throughput sequencing
Platforms:
GPL22765 GPL19757
28 Samples
Download data: CSV, TSV
Series
Accession:
GSE130733
ID:
200130733
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