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Items: 1 to 20 of 143109

1.

A systematic screen identifies Saf5 as a link between splicing and transcription in fission yeast

(Submitter supplied) Splicing is an important step of gene expression regulation in eukaryotes, as there are many mRNA precursors that can be alternatively spliced in different tissues, at different cell cycle phases or under different external stimuli. We have developed several life constructs that allow the quantification of fission yeast splicing in vivo on intact cells, and we have compared their splicing efficiency in a wild type strain and in a prp2-1 (U2AF65) genetic background, showing a clear dependency between Prp2 and a consensus signal at 5’ splicing site (5’SS). more...
Organism:
Schizosaccharomyces pombe
Type:
Expression profiling by high throughput sequencing
Platform:
GPL30658
6 Samples
Download data: TXT
Series
Accession:
GSE242312
ID:
200242312
2.

High Throughput Plant Activation Domain Identification and Mapping

(Submitter supplied) Arabidopsis gene expression is regulated by more than 1,900 transcription factors (TFs), which have been identified genome-wide by the presence of well-conserved DNA binding domains. Activator TFs contain activation domains (ADs) that recruit coactivator complexes; however, for most Arabidopsis TFs, we lack knowledge about the presence, location, and transcriptional strength of their ADs. To address this gap, we experimentally identified Arabidopsis ADs on a proteome-wide scale, finding that over half of Arabidopsis TFs carry an AD. more...
Organism:
Saccharomyces cerevisiae
Type:
Other
Platforms:
GPL19756 GPL27812
164 Samples
Download data: CSV
Series
Accession:
GSE234215
ID:
200234215
3.

Compare transcriptome profile of reference strain and mutant of HapX during A.niger grown on maltose

(Submitter supplied) Transcriptome analysis was performed to identify the differentially expressed genes between hapX mutant and reference strains during their growth on maltose
Organism:
Aspergillus niger
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21721
4 Samples
Download data: XLS
Series
Accession:
GSE260627
ID:
200260627
4.

Dynamic Roles for the Paf1 Complex in Regulating Transcription Elongation and Co-Transcriptional Processes [RNA-seq]

(Submitter supplied) Eukaryotes employ a set of conserved transcription elongation factors to modulate the behavior of RNA polymerase II (RNAPII). Disruptions of one such factor, the Paf1 complex (Paf1C), generate subunit-specific phenotypes, including distinct changes to co-transcriptional histone modifications. How individual Paf1C subunits impact transcription and coupled processes remains ambiguous. By comparing conditional depletion and steady-state deletion of Paf1C subunits, we determine direct and indirect contributions of Paf1C to gene expression in Saccharomyces cerevisiae. more...
Organism:
Saccharomyces cerevisiae; Schizosaccharomyces pombe
Type:
Expression profiling by high throughput sequencing
Platform:
GPL28173
12 Samples
Download data: BW
Series
Accession:
GSE255362
ID:
200255362
5.

Dynamic Roles for the Paf1 Complex in Regulating Transcription Elongation and Co-Transcriptional Processes [ChIP-seq]

(Submitter supplied) Eukaryotes employ a set of conserved transcription elongation factors to modulate the behavior of RNA polymerase II (RNAPII). Disruptions of one such factor, the Paf1 complex (Paf1C), generate subunit-specific phenotypes, including distinct changes to co-transcriptional histone modifications. How individual Paf1C subunits impact transcription and coupled processes remains ambiguous. By comparing conditional depletion and steady-state deletion of Paf1C subunits, we determine direct and indirect contributions of Paf1C to gene expression in Saccharomyces cerevisiae. more...
Organism:
Saccharomyces cerevisiae; Kluyveromyces lactis
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL34174
16 Samples
Download data: BW
Series
Accession:
GSE255361
ID:
200255361
6.

Dynamic Roles for the Paf1 Complex in Regulating Transcription Elongation and Co-Transcriptional Processes [4tU-seq]

(Submitter supplied) Eukaryotes employ a set of conserved transcription elongation factors to modulate the behavior of RNA polymerase II (RNAPII). Disruptions of one such factor, the Paf1 complex (Paf1C), generate subunit-specific phenotypes, including distinct changes to co-transcriptional histone modifications. How individual Paf1C subunits impact transcription and coupled processes remains ambiguous. By comparing conditional depletion and steady-state deletion of Paf1C subunits, we determine direct and indirect contributions of Paf1C to gene expression in Saccharomyces cerevisiae. more...
Organism:
Saccharomyces cerevisiae; Schizosaccharomyces pombe
Type:
Other
Platform:
GPL28173
50 Samples
Download data: BW
Series
Accession:
GSE255360
ID:
200255360
7.

The pleiotropic phenotype of FlbA of Aspergillus niger is explained in part by the activity of seven of its downstream-regulated transcription factors.

(Submitter supplied) Aspergillus niger fulfills an important role in nature in nutrient cycling and is a main cell factory for the industrial production of metabolites and enzymes. Inactivation of flbA in A. niger results in thinner cell walls, increased cell lysis, abolished sporulation, and an increased secretome complexity. A total of 36 transcription factor genes are differentially expressed in ∆flbA. Here, seven of these genes (abaA, aslA, aslB, azf1, htfA, nosA, and srbA) were inactivated. more...
Organism:
Aspergillus niger
Type:
Expression profiling by high throughput sequencing
Platform:
GPL34135
9 Samples
Download data: TSV, XLSX
Series
Accession:
GSE254305
ID:
200254305
8.

Quantitative analysis of wild type and set2 mutant transcriptomes

(Submitter supplied) RNA-seq on total RNA of wild type (WT) and set2 mutant (set2d). To determine the changes in transcriptome profile when set2 gene is delete in comparision to WT cells.
Organism:
Schizosaccharomyces pombe
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13988
4 Samples
Download data: TXT
Series
Accession:
GSE196504
ID:
200196504
9.

The effect of mug174 deletion or red1 deletion mutation on gene expression in the fission yeast Schizosaccharomyces pombe

(Submitter supplied) Our characterization of Mug174 using genetic and biochemical approaches revealed that Mug174 is the Coilin (an integral component of the Cajal body in multicellular organisms) ortholog in the fission yeast S. pombe. To investigate the Mug174 role in shaping transcriptome, we delete the mug174 gene and performed RNA-seq. We found that intron and exon-intron junction reads were elevated in mug174∆, indicating that pre-mRNA splicing is compromised in the absence of Mug174. more...
Organism:
Schizosaccharomyces pombe
Type:
Expression profiling by high throughput sequencing
Platform:
GPL30067
6 Samples
Download data: XLS
Series
Accession:
GSE246256
ID:
200246256
10.

The effect of metal cations on the capture of Pol II-derived nascent transcripts in NET-seq experiments

(Submitter supplied) The goal of this study was to test the effect of metal cations (CaCl2 and MnCl2) during Pol II NET-seq. These metals are readily used in the majority of studies that use NET-seq to analyze Pol II occupancy, but their effect on nascent transcript capture has not been analyzed. Our results suggest that the inclusion of these metals in Pol II NET-seq experiments does not cause a significant change in Pol II occupancy in the untreated control vs. more...
Organism:
Saccharomyces cerevisiae
Type:
Other
Platform:
GPL27812
9 Samples
Download data: BW
Series
Accession:
GSE267082
ID:
200267082
11.

Small molecule inhibitors of fungal ∆(9) fatty acid desaturase as antifungal agent against Candida auris

(Submitter supplied) Candida auris has emerged as a significant healthcare-associated pathogen, posing a serious challenge due to its multidrug-resistant nature. Given the pre-existing constraints in the discovery and provision of new antifungals, there is thus an urgent imperative to design effective strategies to tackle this pressing global concern. Here, we screened a chemical library and identified phenyl-carbohydrazide derivatives with potent activity against both C. more...
Organism:
Candida albicans SC5314; [Candida] auris
Type:
Expression profiling by high throughput sequencing; Other
Platforms:
GPL33190 GPL34459 GPL28368
24 Samples
Download data: TXT
Series
Accession:
GSE267057
ID:
200267057
12.

Genetics, energetics and allostery during a billion years of hydrophobic protein core evolution

(Submitter supplied) Protein folding is driven by the burial of hydrophobic amino acids in a tightly-packed core that excludes water. The genetics, biophysics and evolution of hydrophobic cores are not well understood, in part because of a lack of systematic experimental data on sequence combinations that do - and do not - constitute stable and functional cores. Here we randomize protein hydrophobic cores and evaluate their stability and function at scale. more...
Organism:
Saccharomyces cerevisiae
Type:
Other
Platforms:
GPL19756 GPL31112
16 Samples
Download data: CSV
Series
Accession:
GSE266299
ID:
200266299
13.

Transfection of entomopathogenic Metarhizium species with a novel mycovirus confers hypervirulence against two lepidopteran pests

(Submitter supplied) Although most known mycoviruses are asymptomatic or reduce the virulence of their host fungi, those that confer hypervirulence to entomopathogenic fungus still need to be explored. Here, we discovered and studied a novel mycovirus in Metarhizium flavoviride, isolated from Laodelphax striatellus. Based on molecular analysis, we tentatively designated the mycovirus as Metarhizium flavoviride partitivirus 1 (MfPV1), a novel species in genus Gammapartitivirus, family Partitiviridae. more...
Organism:
Metarhizium anisopliae
Type:
Expression profiling by high throughput sequencing
Platform:
GPL34433
6 Samples
Download data: TXT
Series
Accession:
GSE266301
ID:
200266301
14.

The genetic architecture of protein interaction affinity and specificity

(Submitter supplied) Proteins function in crowded cellular environments in which they must bind to specific target proteins but also avoid binding to many other off-target proteins. In large protein families this task is particularly challenging because many off-target proteins have very similar structures. How this specificity of physical protein-protein interactions in cellular networks is encoded and evolves is not very well understood. more...
Organism:
Escherichia coli; Saccharomyces cerevisiae
Type:
Other
Platforms:
GPL21222 GPL17342
19 Samples
Download data: TXT
Series
Accession:
GSE245326
ID:
200245326
15.

Expression data from Saccharomyces cerevisiae

(Submitter supplied) Reprogramming a non-methylotrophic industrial host, such as Saccharomyces cerevisiae, to a synthetic methylotroph reprents a huge challenge due to the complex regulation in yeast. Through TMC strategy together with ALE strategy, we completed a strict synthetic methylotrophic yeast that could use methanol as the sole carbon source. However, how cells respond to methanol and remodel cellular metabolic network on methanol were not clear. more...
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21656
6 Samples
Download data: CSV
Series
Accession:
GSE173802
ID:
200173802
16.

Melanization of fungal necromass drives the upregulation of multiple chitinase, protease, and laccase genes when being degraded by Trichoderma reesei

(Submitter supplied) Fungal necromass in soil represents the stable carbon pools. While fungi are known to decompose fungal necromass, how fungi decomopose melanin, remains poorly understood. Recently, Trichoderma species was found to be one of the most commonly associated fungi in soil, we have used a relevant fungal species, Trichoderma reesei, to characterized Genes involved in the decomposition of melanized and non-melanized necromass from Hyaloscypha bicolor.
Organism:
Trichoderma reesei
Type:
Expression profiling by high throughput sequencing
Platform:
GPL34370
9 Samples
Download data: CSV
Series
Accession:
GSE263516
ID:
200263516
17.

Tracking live-cell single-molecule dynamics enables measurements of heterochromatin-associated protein-protein interactions

(Submitter supplied) Visualizing and measuring molecular-scale interactions in living cells represents a major challenge, but recent advances in microscopy are bringing us closer to achieving this goal. Single-molecule super-resolution microscopy enables high-resolution and sensitive imaging of the positions and movement of molecules in living cells. HP1 proteins are important regulators of gene expression because they selectively bind and recognize H3K9 methylated (H3K9me) histones to form heterochromatin-associated protein complexes that silence gene expression. more...
Organism:
Schizosaccharomyces pombe
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL20584
5 Samples
Download data: BW
Series
Accession:
GSE263472
ID:
200263472
18.

Investigating determinants of aneuploidy toxicity using gene duplication in Saccharomyces cerevisiae

(Submitter supplied) Aneuploidy has a myriad of consequences for health and disease, yet models of aneuploidy toxicity are still widely debated. To distinguish the effects of specific genes from the generalized burden of chromosome amplification, we measured the effects of duplicating individual genes in euploid cells as well as in select aneuploids using a barcoded plasmid library. We analyzed the responses of cells with and without extra chromosomes, as well as those with and without RNA-binding protein Ssd1. more...
Organism:
Saccharomyces cerevisiae
Type:
Other
Platform:
GPL21656
83 Samples
Download data: CSV
Series
Accession:
GSE263221
ID:
200263221
19.

Integrative Omics reveals changes in the cellular landscape of yeast without peroxisomes

(Submitter supplied) Peroxisomes are organelles that are crucial for cellular metabolism. However, these organelles play also important roles in non-metabolic processes, such as signalling. To uncover the consequences of peroxisome deficiency, we compared two extremes, namely Saccharomyces cerevisiae wild-type and pex3 cells, which lack functional peroxisomes, employing transcriptomics and quantitative proteomics technology. more...
Organism:
Saccharomyces cerevisiae BY4741
Type:
Expression profiling by high throughput sequencing
Platform:
GPL28475
6 Samples
Download data: CSV
Series
Accession:
GSE261289
ID:
200261289
20.

RiboSeq and mSeq of two yeast strains

(Submitter supplied) We report on how the absence of expansion segment 7S from the yeast ribosome alters A-site occupancy along transcripts. This has consequence for local translation rates and protein fidelity.
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by high throughput sequencing; Other
Platform:
GPL26302
11 Samples
Download data: TXT
Series
Accession:
GSE220642
ID:
200220642
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