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Links from GEO DataSets

Items: 20

1.

RNA-seq of RNAs immunoprecipitated with eIF4E1c and eiF4E1c in early zebrafish embryos

(Submitter supplied) To investigate the mRNAs that are bound by eIF4E1b and eIF4E1c, we performed RNA immunoprecipitation (RIP) experiments using anti-GFP beads and transgenic embryos expressing GFP-eIF4E1b or GFP-eIF4E1c at the 8-cell stage.
Organism:
Danio rerio
Type:
Expression profiling by high throughput sequencing; Other
Platform:
GPL24995
11 Samples
Download data: TSV
Series
Accession:
GSE233570
ID:
200233570
2.

RNA-seq of female gonads isolated from juvenile eif4e1b mutant and wild-type zebrafish

(Submitter supplied) The mRNA cap-binding protein eIF4E1b is critical for female germline development in zebrafish. To study the effect of eIF4E1b loss in zebrafish, we isolated gonads with a high expression of ziwi:GFP (female germline marker) from wild-type and eif4e1b mutant juveniles and performed RNA-seq.
Organism:
Danio rerio
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24995
6 Samples
Download data: TSV
Series
Accession:
GSE241537
ID:
200241537
3.

Germ-cell specific eIF4E1b regulates maternal mRNA translation to ensure zygotic genome activation [Ribo-seq]

(Submitter supplied) Translation of maternal mRNAs is detected before transcription of zygotic genes and is essential for mammalian embryo development. How certain maternal mRNAs are selected for translation instead of degradation and how this burst of translation affects zygotic genome activation remains unknown. Using gene-edited mice, we document that the oocyte-specific eukaryotic translation initiation factor 4E family member 1b (eIF4E1b) is the regulator of maternal mRNA expression that ensures subsequent reprogramming of the zygotic genome. more...
Organism:
Mus musculus
Type:
Other
Platform:
GPL24247
15 Samples
Download data: BW, CSV, TSV
Series
Accession:
GSE230019
ID:
200230019
4.

Germ-cell specific eIF4E1b regulates maternal mRNA translation to ensure zygotic genome activation [NOMe-seq]

(Submitter supplied) Translation of maternal mRNAs is detected before transcription of zygotic genes and is essential for mammalian embryo development. How certain maternal mRNAs are selected for translation instead of degradation and how this burst of translation affects zygotic genome activation remains unknown. Using gene-edited mice, we document that the oocyte-specific eukaryotic translation initiation factor 4E family member 1b (eIF4E1b) is the regulator of maternal mRNA expression that ensures subsequent reprogramming of the zygotic genome. more...
Organism:
Mus musculus
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL21103
192 Samples
Download data: TSV
Series
Accession:
GSE200685
ID:
200200685
5.

Germ cell-specific eIF4E1b regulates maternal mRNA translation to ensure zygotic genome activation

(Submitter supplied) Translation of maternal mRNAs is detected before transcription of zygotic genes and is essential for mammalian embryo development. How certain maternal mRNAs are selected for translation instead of degradation and how this burst of translation affects zygotic genome activation remain unknown. Using gene-edited mice, we document that the oocyte-specific eukaryotic translation initiation factor 4E family member 1b (eIF4E1b) is the regulator of maternal mRNA expression that ensures subsequent reprogramming of the zygotic genome. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Methylation profiling by high throughput sequencing; Other
Platforms:
GPL21103 GPL24247
602 Samples
Download data: BW, TSV
Series
Accession:
GSE180218
ID:
200180218
6.

Germ-cell specific eIF4E1b regulates maternal mRNA translation to ensure zygotic genome activation [RIP-seq]

(Submitter supplied) Translation of maternal mRNAs is detected before transcription of zygotic genes and is essential for mammalian embryo development. How certain maternal mRNAs are selected for translation instead of degradation and how this burst of translation affects zygotic genome activation remains unknown. Using gene-edited mice, we document that the oocyte-specific eukaryotic translation initiation factor 4E family member 1b (eIF4E1b) is the regulator of maternal mRNA expression that ensures subsequent reprogramming of the zygotic genome. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21103
24 Samples
Download data: CSV, TSV
Series
Accession:
GSE180217
ID:
200180217
7.

Germ-cell specific eIF4E1b regulates maternal mRNA translation to ensure zygotic genome activation [RNA-seq]

(Submitter supplied) Translation of maternal mRNAs is detected before transcription of zygotic genes and is essential for mammalian embryo development. How certain maternal mRNAs are selected for translation instead of degradation and how this burst of translation affects zygotic genome activation remains unknown. Using gene-edited mice, we document that the oocyte-specific eukaryotic translation initiation factor 4E family member 1b (eIF4E1b) is the regulator of maternal mRNA expression that ensures subsequent reprogramming of the zygotic genome. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21103
371 Samples
Download data: CSV, TSV
Series
Accession:
GSE180206
ID:
200180206
8.

Sequential regulation of maternal mRNAs through a conserved cis-acting element in their 3'UTRs

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Drosophila melanogaster
Type:
Expression profiling by high throughput sequencing; Other
Platform:
GPL19132
13 Samples
Download data: BIGWIG, TXT
Series
Accession:
GSE119458
ID:
200119458
9.

Sequential regulation of maternal mRNAs through a conserved cis-acting element in their 3’UTRs [II]

(Submitter supplied) Maternal mRNAs are synthesized during oogenesis to initiate the development of future generations. Some maternal mRNAs are determinants of somatic or germline fate and must be translationally repressed until embryogenesis. However, the translational repressors themselves are also temporally regulated. We use polar granule component (pgc), a Drosophila maternal mRNA, as a model system to ask how maternal mRNAs are repressed while the regulatory landscape is continually shifting. more...
Organism:
Drosophila melanogaster
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19132
1 Sample
Download data: BIGWIG, TXT
Series
Accession:
GSE119457
ID:
200119457
10.

Sequential regulation of maternal mRNAs through a conserved cis-acting element in their 3’UTRs [I]

(Submitter supplied) Maternal mRNAs are synthesized during oogenesis to initiate the development of future generations. Some maternal mRNAs are determinants of somatic or germline fate and must be translationally repressed until embryogenesis. However, the translational repressors themselves are also temporally regulated. We use polar granule component (pgc), a Drosophila maternal mRNA, as a model system to ask how maternal mRNAs are repressed while the regulatory landscape is continually shifting. more...
Organism:
Drosophila melanogaster
Type:
Expression profiling by high throughput sequencing; Other
Platform:
GPL19132
12 Samples
Download data: TXT
Series
Accession:
GSE119456
ID:
200119456
11.

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
12.

Maternal mRNA deadenylation and allocation via Rbm14 condensates facilitate vertebrate blastula development

(Submitter supplied) Early embryonic development depends on proper utilization and clearance of maternal transcriptomes. How these processes are spatiotemporally regulated remains unclear. Here we show that nuclear RNA-binding protein Rbm14 and maternal mRNAs co-phase separate into cytoplasmic condensates to facilitate vertebrate blastula-to-gastrula development. In zebrafish, Rbm14 condensates were highly abundant in blastomeres and markedly reduced after prominent activation of zygotic transcription. more...
Organism:
Danio rerio; Mus
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL29655 GPL21741
21 Samples
Download data: CSV
Series
Accession:
GSE179035
ID:
200179035
13.

CERES is an eIF4E-interacting protein that forms non-canonical translation initiation complexes and modulates translation during the diel cycle in plants

(Submitter supplied) Translation is a fundamental step in gene expression that regulates multiple developmental and stress responses. One key step of translation is the association between eIF4E and eIF4G. This process is regulated in different eukaryotes by proteins which bind to eIF4E and block the formation of the eIF4E/eIF4G complex. Here, we report the discovery of CERES, the first functional eIF4E regulator described in plants. more...
Organism:
Arabidopsis thaliana
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13222
18 Samples
Download data: XLS
Series
Accession:
GSE124290
ID:
200124290
14.

The CCR4-NOT complex suppresses untimely translational activation of maternal mRNAs.

(Submitter supplied) Control of mRNA poly(A) tail has central role to regulate mRNA metabolism: translation efficiency and mRNA stability. Gene expression in maturing oocytes largely relies on the regulation of mRNA metabolism as they are transcriptionally silent. The CCR4-NOT complex is a major deadenylase for mammals and regulates poly(A) tails of maternal mRNAs, however their function to translational regulation was not well understood. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
8 Samples
Download data: TXT
Series
Accession:
GSE224308
ID:
200224308
15.

Transcriptome analysis of wild-type and maternal ybx1 mutant zebrafish embryos during early development

(Submitter supplied) To study the function of zebrafish Ybx1 during early embryogenesis, we generated maternal ybx1 (Mybx1) mutant using CRISPR/Cas9 and report the transcriptome-wide changes in comparison to wild-type (WT) embryos. Our analysis reveals a dramatic loss of maternal mRNA decay and zygotic genome activation in Mybx1 embryos during maternal-to-zygotic transition.
Organism:
Danio rerio
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18413
4 Samples
Download data: TXT
Series
Accession:
GSE108924
ID:
200108924
16.

The functions of m6A and Ythdf2 during zebrafish early development

(Submitter supplied) We report the m6A methylation maps of zebrafish embryos during early development, and transcriptome-wide changes occured in ythdf2 LOF mutant embryos. Our study reveals the m6A-dependent RNA decay as a previously unidentified maternal mode mechanism to regulate maternal mRNA clearance during zebrafish   MZT, highlighting the critical role of the m6A mRNA methylation in animal development.
Organism:
Danio rerio
Type:
Expression profiling by high throughput sequencing; Other
Platform:
GPL18413
76 Samples
Download data: BED, XLSX
Series
Accession:
GSE79213
ID:
200079213
17.

Mitosis-related phosphorylation of the eukaryotic translation suppressor 4E-BP1 and its interaction with eukaryotic translation initiation factor 4E (eIF4E)

(Submitter supplied) Eukaryotic translation initiation factor 4E (eIF4E)–binding protein 1 (4E-BP1) inhibits cap-dependent translation in eukaryotes by competing with eIF4G for an interaction with eIF4E. Phos-phorylation at Ser-83 of 4E-BP1 occurs during mitosis through the activity of cyclin-dependent kinase 1 (CDK1)/cyclin B rather than through canonical mTOR kinase activity. Here, we investi-gated the interaction of eIF4E with 4E-BP1 or eIF4G during interphase and mitosis. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11154
20 Samples
Download data: TXT
Series
Accession:
GSE131668
ID:
200131668
18.

A widespread alternate form of cap-dependent mRNA translation initiation

(Submitter supplied) We report the application of polysome profiling sequencing technology for high-throughput transcriptomics and translatomics in mammalian cells. We compare reduction of Dap5 to control in metastatic breast cancer cells in transcription and polysome enriched translation using RNA sequencing. Genome-wide transcriptomic and translatomic analyses indicate that DAP5 is required for translation of many transcription factor and receptor capped mRNAs and their mRNA targets involved in cell survival, motility, DNA repair and translation initiation, among other mRNAs.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11154
14 Samples
Download data: TXT
19.

The Translation Initiation Factor eIF3h Targets Specific Transcripts to Polysomes during Embryogenesis

(Submitter supplied) We have sequenced the polysome-associated translating mRNAs from stage-matched wild-type and eif3ha morphant embryos at ~24 hpf stage to identify transcripts translationally regulated by eIF3ha. As a control, we have also sequenced total mRNAs from the stage-matched wild-type and eif3ha morphants as well at ~ 24 hpf.
Organism:
Danio rerio
Type:
Expression profiling by high throughput sequencing
Platform:
GPL15583
4 Samples
Download data: TSV
Series
Accession:
GSE44584
ID:
200044584
20.

TRIBE editing reveals specific mRNA targets of eIF4E-BP in Drosophila and in mammals

(Submitter supplied) 4E-BP (eIF4E-BP) represses translation initiation by binding to the 5’cap-binding protein eIF4E and inhibiting its activity. Although 4E-BP has been shown to be important in growth control, stress response, cancer, neuronal activity and mammalian circadian rhythms, it is not understood how it preferentially represses a subset of mRNAs. We successfully used hyperTRIBE (Targets of RNA-binding proteins identified by editing) to identify in vivo 4E-BP mRNA targets in both Drosophila and mammals under conditions known to activate 4E-BP. more...
Organism:
Homo sapiens; Drosophila melanogaster
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL18573 GPL19132
35 Samples
Download data: BW, TXT
Series
Accession:
GSE153346
ID:
200153346
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