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Items: 1 to 20 of 10857

1.

The establishment of HP1-independent heterochromatin reveals an essential role for HP1 proteins in maintaining epigenetic memory.

(Submitter supplied) H3K9 methylation (H3K9me) marks transcriptionally silent genomic regions called heterochromatin. A conserved class of HP1 proteins are critically required to establish and maintain heterochromatin. HP1 proteins bind to H3K9me, recruit factors that promote heterochromatin formation, and oligomerize to form phase-separated condensates. We do not understand how HP1 protein binding to heterochromatin establishes and maintains transcriptional silencing. more...
Organism:
Schizosaccharomyces pombe
Type:
Expression profiling by high throughput sequencing
Platform:
GPL28961
31 Samples
Download data: XLSX
Series
Accession:
GSE233333
ID:
200233333
2.

Isw1 contributes to cohesin association with centromeres and pericentromeric regions

(Submitter supplied) Cohesin is a highly conserved, multiprotein complex whose canonical function is to hold sister chromatids together to ensure accurate chromosome segregation. Cohesin association with chromatin relies on the separate Scc2-Scc4 complex that enables cohesin ring opening and topological entrapment of sister DNAs. Cohesin loading at centromeres also requires the CTF19 kinetochore subcomplex that recruits Scc2-Scc4, ensuring efficient and targeted cohesin binding. more...
Organism:
Saccharomyces cerevisiae; Schizosaccharomyces pombe
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL29170
4 Samples
Download data: BW
Series
Accession:
GSE232315
ID:
200232315
3.

The establishment of HP1-independent heterochromatin reveals an essential role for HP1 proteins in maintaining epigenetic memory

(Submitter supplied) H3K9 methylation (H3K9me) marks transcriptionally silent genomic regions called heterochromatin. A conserved class of HP1 proteins are critically required to establish and maintain heterochromatin. HP1 proteins bind to H3K9me, recruit factors that promote heterochromatin formation, and oligomerize to form phase-separated condensates. We do not understand how HP1 protein binding to heterochromatin establishes and maintains transcriptional silencing. more...
Organism:
Schizosaccharomyces pombe
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL20584
24 Samples
Download data: BW, FA, FASTA, GFF, GFF3
Series
Accession:
GSE231618
ID:
200231618
4.

The conserved RNA-binding protein Seb1 promotes cotranscriptional ribosomal RNA processing by controlling RNA polymerase I progression

(Submitter supplied) Transcription by RNA polymerase I (RNAPI) represents the majority of the transcriptional activity in eukaryotic cells and is associated with the production of mature ribosomal rRNAs (rRNAs). As several rRNA maturation steps are coupled to RNAPI transcription, the rate of RNAPI elongation directly influences processing of nascent rRNA, and changes in RNAPI transcription rate can result in alternative rRNA processing pathways in response to growth conditions and stress. more...
Organism:
Schizosaccharomyces pombe
Type:
Other
Platform:
GPL17225
6 Samples
Download data: BW
Series
Accession:
GSE212930
ID:
200212930
5.

An essential role for the Ino80 chromatin remodeling complex in regulation of gene expression during cellular quiescence

(Submitter supplied) Cellular quiescence is an important physiological state both in unicellular and multicellular eukaryotes. Quiescent cells are halted for proliferation and stop the cell cycle at the G0 stage. Using fission yeast as a model organism, we have previously found that several subunits of a conserved chromatin remodeling complex, Ino80C (INOsitol requiring nucleosome remodeling factor), are required for survival in quiescence. more...
Organism:
Schizosaccharomyces pombe
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL30658
97 Samples
Download data: BIGWIG, TXT
Series
Accession:
GSE200378
ID:
200200378
6.

Duf89 abets lncRNA control of fission yeast phosphate homeostasis via its antagonism of precocious lncRNA transcription termination

(Submitter supplied) This RNA-Seq analysis compares gene expression of the Duf89 null mutant (duf89∆) contrasting to the WT in the fission yeast S. pombe
Organism:
Schizosaccharomyces pombe
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL22682 GPL28961
6 Samples
Download data: XLSX
Series
Accession:
GSE216299
ID:
200216299
7.

The LARP1 homolog Slr1p controls the stability and expression of proto-5’TOP mRNAs in fission yeast

(Submitter supplied) In vivo metabolic labelling of S. pombe RNA to measure transcriptome-wide mRNA half-lives
Organism:
Schizosaccharomyces pombe
Type:
Expression profiling by high throughput sequencing; Other
Platform:
GPL28961
36 Samples
Download data: TSV
Series
Accession:
GSE200633
ID:
200200633
8.

Fission yeast TORC1 promotes cell proliferation through Sfp1, a transcription factor involved in ribosome biogenesis

(Submitter supplied) To study the TORC1-mediated transcriptional regulation of the genes involved in ribosome biosynthesis in fission yeast
Organism:
Schizosaccharomyces pombe
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16192
4 Samples
Download data: XLSX
Series
Accession:
GSE201580
ID:
200201580
9.

Spt3 and Spt8 are involved in the formation of a silencing boundary by interacting with TATA-binding protein

(Submitter supplied) In Saccharomyces cerevisiae, a heterochromatin-like chromatin structure called the silencing region is present at the telomere as a complex of Sir2, Sir3, and Sir4. Sir2 is a histone deacetylase, and Sir3 and Sir4 promote spreading of the silencing region at the telomere. Histone acetyltransferases restrict the silencing region. Here, we show that Spt3 and Spt8 block the spread of silencing regions. more...
Organism:
Saccharomyces cerevisiae; Schizosaccharomyces pombe
Type:
Expression profiling by array
Platform:
GPL2529
3 Samples
Download data: CEL, CHP
Series
Accession:
GSE220290
ID:
200220290
10.

Detection of Q-modification in RNAs from S. pombe and S. flexneri via reverse transcription using RT-KTq I614Y (Q-MaP-Seq)

(Submitter supplied) In most eukaryotes and bacteria, queuosine (Q) replaces the guanosine at the wobble position of tRNAs harboring a GUN anticodon. To faithfully detect Q-modification in RNAs from Schizosaccharomyces pombe and Shigella flexneri, Q-MaP-Seq was established and applied to tRNAs from S. pombe WT (AEP1) cells and Shigella flexneri WT cells and tgt∆ cells. Q-modification of in vitro-transcribed RNAs and RNAs isolated from S. more...
Organism:
Shigella flexneri; Schizosaccharomyces pombe
Type:
Expression profiling by high throughput sequencing; Other
Platforms:
GPL16192 GPL30040
30 Samples
Download data: XLSX
Series
Accession:
GSE216921
ID:
200216921
11.

Genome-wide localization of Swi6 and H3-Lys9-me2 in wt and mutant starins of S. pombe

(Submitter supplied) ChIP-on-ChIP experiments were performed to quantitate the genome-wide localization of heterochromatin proteins Swi6 and H3-Lys9-me2 in wild type versus polalpha mutant swi7H4, Pol delta mutant, dts2 and cut4 mutant cut4-993. Our results indicate that the localization of Swi6 and H3-Lys7-me2 at heterochromaitn regions, like centromere, telomere and mating-type is abrogated in the swi7H4, dts2 and cut4 mutants.
Organism:
Schizosaccharomyces pombe
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL16383
8 Samples
Download data: TXT
Series
Accession:
GSE198590
ID:
200198590
12.

Chromatin localization of nucleophosmin determines the sorting and compartmentalization of ribosome biogenesis

(Submitter supplied) Assembly of eukaryotic ribosomes begins in the nucleolus, a compartmentalized membraneless organelle. Although the two ribosomal subunits, 40S and 60S, assemble independently, it remains unknown if these particles are physically sorted as they assemble and how they partition from the central chromatin compartment into the outer nucleolar regions, where maturation occurs. In this study, we show that nucleophosmin specifically mediates the assembly of nascent 60S subunits and that this specificity is determined by its chromatin localization at the rDNA sites encoding for 60S subunit rRNA. more...
Organism:
Schizosaccharomyces pombe
Type:
Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing
Platform:
GPL22681
64 Samples
Download data: TDF
Series
Accession:
GSE156203
ID:
200156203
13.

Physiological and molecular characterization of yeast cultures pre-adapted for fermentation of lignocellulosic hydrolysate

(Submitter supplied) To reach an economically feasible bioethanol process from lignocellulose, efficient fermentation by yeast of all sugars present in the hydrolysate has to be achieved. However, when exposed to lignocellulosic hydrolysate, Saccharomyces cerevisiae is challenged with a variety of inhibitors that reduce yeast viability, growth and fermentation rate, and in addition damage cellular structures. In order to evaluate the yeast capability to adapt to lignocellulosic hydrolysates and to investigate the yeast molecular response to inhibitors, fed-batch cultivation of an industrial S. more...
Organism:
Schizosaccharomyces pombe; Saccharomyces cerevisiae
Type:
Expression profiling by array
Platform:
GPL2529
10 Samples
Download data: CEL, XLSX
Series
Accession:
GSE218764
ID:
200218764
14.

Gene expression profile during Ebselen treatment in budding yeast

(Submitter supplied) Ebselen is synthetic selenium containing organic compound. It exhibits glutathione peroxidase (GSH-Px) like activity hence acts as a potent antioxidant therefore has been widely used in the treatment of various diseases. In contrast, certain studies also demonstrate its toxic nature; however its mechanism of action is not well understood. Presently, Ebselen has been used at 100 µM concentration for the elucidation of its molecular and cellular mechanism of action. more...
Organism:
Schizosaccharomyces pombe; Saccharomyces cerevisiae
Type:
Expression profiling by array
Platform:
GPL2529
4 Samples
Download data: CEL
Series
Accession:
GSE41711
ID:
200041711
15.

Cellular responses to long-term phosphate starvation of fission yeast: Maf1 determines fate choice between quiescence and death associated with aberrant tRNA biogenesis

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Schizosaccharomyces pombe
Type:
Expression profiling by high throughput sequencing
Platform:
GPL28961
35 Samples
Download data: XLSX
Series
Accession:
GSE217953
ID:
200217953
16.

Cellular responses to long-term phosphate starvation of fission yeast: Maf1 determines fate choice between quiescence and death associated with aberrant tRNA biogenesis (CHX experiments)

(Submitter supplied) This RNA-Seq analysis compares gene expression of fission yeast cells (Schizosaccharomyces pombe) at various times after phosphate starvation (2, 4, and 8 HR) either with 100 µg/ml cycloheximide or without drug contrasting to the cells grown in phosphate replete conditions (0HR) in the absence of the drug.
Organism:
Schizosaccharomyces pombe
Type:
Expression profiling by high throughput sequencing
Platform:
GPL28961
21 Samples
Download data: XLSX
Series
Accession:
GSE217952
ID:
200217952
17.

Cellular responses to long-term phosphate starvation of fission yeast: Maf1 determines fate choice between quiescence and death associated with aberrant tRNA biogenesis

(Submitter supplied) This RNA-Seq analysis compares gene expression of fission yeast (Schizosaccharomyces pombe) strains prior to phosphate starvation (0 HR) and at various times after phosphate starvation (4, 8, 12, 24, 36, and 48 HR) contrasting to the WT fission yeast S. pombe cells grown in phosphate replete conditions (WT 0HR)
Organism:
Schizosaccharomyces pombe
Type:
Expression profiling by high throughput sequencing
Platform:
GPL28961
14 Samples
Download data: TXT, XLSX
Series
Accession:
GSE213459
ID:
200213459
18.

ORE-seq: genome-wide absolute occupancy measurement by restriction enzyme accessibilities

(Submitter supplied) Digestion with restriction enzymes is a classical approach for probing DNA accessibility in chromatin. It allows to monitor both the cut and the uncut fraction and thereby the determination of accessibility or occupancy (= 1- accessibility) in absolute terms as the percentage of cut or uncut out of the total molecules. The here presented protocol takes this classical approach to the genome-wide level. more...
Organism:
Saccharomyces cerevisiae; Schizosaccharomyces pombe
Type:
Other
Platforms:
GPL30978 GPL30979
21 Samples
Download data: BW
Series
Accession:
GSE189142
ID:
200189142
19.

Chromatin remodeling by antisense Pol II primes efficient Pol III transcription

(Submitter supplied) The packaging of the genetic material into chromatin imposes the remodeling of this barrier to allow efficient transcription. RNA polymerase II activity is associated with several histone modification complexes that enforce remodeling. How RNA polymerase III (Pol III) counteracts the inhibitory effect of chromatin is unknown. We report here that antisense RNA Polymerase II (Pol II) transcription is critical to prime and maintain nucleosome depletion at Pol III loci and allow efficient Pol III recruitment upon re-initiation of growth from stationary phase. more...
Organism:
Schizosaccharomyces pombe
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL17225
12 Samples
Download data: BW, TXT
Series
Accession:
GSE193552
ID:
200193552
20.

Mechanistic insights into the role of the canonical poly(A) polymerase Pla1 in RNA surveillance by the fission yeast MTREC complex

(Submitter supplied) In this study we analysed the functional relevance of the interaction between Pla1 and the MTREC complex core component Red1 using various high throughput sequencing analyses performed on different Pla1-Red1 interaction mutants.Our analyses revealed that as part of MTREC complex, Pla1 hyper-adenylates Cryptic Unstable Transcripts (CUTs) for their efficient degradation. Interestingly, our H3K9(me)2 ChIP seq. more...
Organism:
Schizosaccharomyces pombe
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing; Other
Platforms:
GPL28961 GPL31123
30 Samples
Download data: BW
Series
Accession:
GSE206106
ID:
200206106
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