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Links from GEO DataSets

Items: 20

1.

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
2.

mRNAs that co-purify with OMA-1 in the C. elegans germline

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Caenorhabditis elegans
Type:
Other
Platforms:
GPL13657 GPL200
13 Samples
Download data: CEL, TXT
Series
Accession:
GSE54518
ID:
200054518
3.

mRNAs that co-purify with OMA-1 in the C. elegans germline (sequencing)

(Submitter supplied) The oocytes of most animals arrest at diplotene or diakinesis, but resume meiosis (meiotic maturation) in response to hormones. In C. elegans, maturation of the –1 oocyte requires the presence of sperm, Gas-adenylate cyclase-PKA signaling in the gonadal sheath cells, and germline function of two Tis11-like CCCH zinc-finger proteins, OMA-1 and OMA-2 (OMA proteins). Prior studies indicate that the OMA proteins redundantly repress the translation of specific mRNAs in oocytes (zif-1, mom-2, nos-2, glp-1) and early embryos (mei-1). more...
Organism:
Caenorhabditis elegans
Type:
Other
Platform:
GPL13657
1 Sample
Download data: TXT
Series
Accession:
GSE54517
ID:
200054517
4.

mRNAs that co-purify with OMA-1 in the C. elegans germline (microarray)

(Submitter supplied) The oocytes of most animals arrest at diplotene or diakinesis, but resume meiosis (meiotic maturation) in response to hormones. In C. elegans, maturation of the –1 oocyte requires the presence of sperm, Gas-adenylate cyclase-PKA signaling in the gonadal sheath cells, and germline function of two Tis11-like CCCH zinc-finger proteins, OMA-1 and OMA-2 (OMA proteins). Prior studies indicate that the OMA proteins redundantly repress the translation of specific mRNAs in oocytes (zif-1, mom-2, nos-2, glp-1) and early embryos (mei-1). more...
Organism:
Caenorhabditis elegans
Type:
Other
Platform:
GPL200
12 Samples
Download data: CEL
Series
Accession:
GSE54513
ID:
200054513
5.

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
6.

Transcriptome assay of maternal mRNA degradation in ERK-deleted oocytes

(Submitter supplied) We analyzed the functions of ERK in maternal mRNA degradation in mouse oocytes. By comparing the degradation of transcripts in WT oocytes and KO oocytes, we are able to know the defects in maternal mRNA clearance in ERK-deleted oocytes, and identified the ERK target genes in oocyte maturation.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
4 Samples
Download data: TXT
Series
Accession:
GSE92317
ID:
200092317
7.

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
8.

Genome-wide analysis reveals a switch in the translational program upon oocyte meiotic resumption

(Submitter supplied) Examination of ribosome-bound mRNA at five timepoints (in duplicates) during oocyte meiosis (prophase I (0 hrs), early pro-metaphase I (2 hrs), pro-metaphase I (4 hrs), late pro-metaphase I (6 hrs), and late metaphase I (8 hrs)).
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21103
20 Samples
Download data: CSV
Series
Accession:
GSE135525
ID:
200135525
9.

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
10.

The APC/CFZY-1/Cdc20 complex coordinates with OMA-1 to regulate the oocyte-to-embryo transition in C. elegans

(Submitter supplied) During oocyte maturation and the oocyte-to-embryo transition, key developmental regulators such as RNA-binding proteins coordinate translation of particular mRNAs and related developmental processes by binding to their cognate maternal mRNAs. In the nematode C. elegans, these processes are regulated by a set of CCCH zinc finger proteins. OMA-1 and OMA-2 are two functionally redundant CCCH zinc finger proteins that turnover rapidly during the first embryonic cell division. more...
Organism:
Caenorhabditis elegans
Type:
Expression profiling by high throughput sequencing
Platform:
GPL26672
21 Samples
Download data: TXT, XLSX
Series
Accession:
GSE181115
ID:
200181115
11.

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
12.

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
13.

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
14.

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
15.

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
16.

C. elegans DLC-1 is a component of diverse ribonucleoprotein complexes

(Submitter supplied) Ribonucleoprotein complexes, which contain mRNAs and their regulator proteins, carry out post-transcriptional control of gene expression. The function of many RNA-binding proteins depends on their association with cofactors. Here we use a genomic approach to identify transcripts associated with DLC-1, a protein previously identified as a cofactor of two unrelated RNA-binding proteins that act in the C. more...
Organism:
Caenorhabditis elegans
Type:
Other
Platform:
GPL18245
10 Samples
Download data: XLSX
Series
Accession:
GSE115281
ID:
200115281
17.

CNOT6L Couples the Selective Degradation of Maternal Transcriptsto Meiotic Cell Cycle Progression in Mouse Oocyte

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21273
36 Samples
Download data: TXT
Series
Accession:
GSE118564
ID:
200118564
18.

CNOT6L Couples the Selective Degradation of Maternal Transcriptsto Meiotic Cell Cycle Progression in Mouse Oocyte [polysome RNA-seq]

(Submitter supplied) Purpose: The goals of this study are to study the function of Cnot6l during oocyte maturation . Methods: Comparing the polysome-bounded transcripts at GV, MI and MII stage in WT and Cnot6l-/- oocytes by RNA sequencing. Results: Using an optimized data analysis workflow, we mapped about 15 million sequence reads per sample to the mouse genome (build mm9) and identified 23236 transcripts with TopHat workflow. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21273
12 Samples
Download data: TXT
Series
Accession:
GSE118563
ID:
200118563
19.

CNOT6L Couples the Selective Degradation of Maternal Transcriptsto Meiotic Cell Cycle Progression in Mouse Oocyte [total RNA-seq]

(Submitter supplied) Purpose: The goals of this study are to study the function of Cnot6l during oocyte maturation and the differences between loss of Cnot6l and Btg4 during oocyte maturation. Methods:Comparing the degration of transcripts at different stage in WT, Btg4-/- and Cnot6l-/- oocytes by RNA sequencing. Results: Using an optimized data analysis workflow, we mapped about 15 million sequence reads per sample to the mouse genome (build mm9) and identified 23236 transcripts with TopHat workflow. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21273
24 Samples
Download data: TXT
Series
Accession:
GSE118562
ID:
200118562
20.

Nuclear Envelope Retention of LINC Complexes Is Promoted by SUN-1 Oligomerization in the Caenorhabditis elegans Germ Line

(Submitter supplied) SUN (Sad1 and UNC-84) and KASH (Klarsicht, ANC-1 and Syne homology) proteins are constituents of the inner and outer nuclear membranes. They interact in the perinuclear space via carboxy-terminal SUN-KASH domains to form the Linker of Nucleoskeleton and Cytoskeleton (LINC) complex thereby bridging the nuclear envelope. LINC complexes sustain numerous biological processes by connecting chromatin with the cytoplasmic force generating machinery. more...
Organism:
Caenorhabditis elegans
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13657
5 Samples
Download data: TXT
Series
Accession:
GSE76773
ID:
200076773
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