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Links from GEO DataSets

Items: 20

1.

Spt6 directly interacts with Cdc73 and is required for Paf1C occupancy at active genes in Saccharomyces cerevisiae

(Submitter supplied) The Paf1 complex (Paf1C) is a conserved transcription elongation factor that regulates transcription elongation efficiency, facilitates co-transcriptional histone modifications, and impacts molecular processes linked to RNA synthesis, such as polyA site selection. Coupling of the activities of Paf1C to transcription elongation requires its association with RNA polymerase II (Pol II). Mutational studies in yeast identified Paf1C subunits Cdc73 and Rtf1 as important mediators of Paf1C association with Pol II on active genes. more...
Organism:
Saccharomyces cerevisiae
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL31112
60 Samples
Download data: BW
Series
Accession:
GSE201436
ID:
200201436
2.

Architecture of the RNA polymerase II-Paf1C-TFIIS transcription elongation complex

(Submitter supplied) 2 transcription elongation complex
Organism:
Saccharomyces cerevisiae BY4741
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20615
6 Samples
Download data: GTF, TXT
Series
Accession:
GSE95556
ID:
200095556
3.

The Histone Modification Domain of Paf1 Complex Subunit Rtf1 Promotes H2B Ubiquitylation Through a Direct Interaction with the Ubiquitin Conjugase Rad6

(Submitter supplied) Transcription by RNA polymerase II is regulated by epigenetic modifications to the chromatin template. The mono-ubiquitylation of H2B is established during transcription elongation and broadly impacts chromatin architecture and gene expression. The Polymerase Associated Factor 1 complex (Paf1C) is required for H2B ubiquitylation through an unknown mechanism. Here, we find that a 66-amino acid histone modification domain (HMD) within the Rtf1 subunit of Paf1C promotes H2B ubiquitylation in cells lacking all Paf1C members and present the crystal structure of this domain. more...
Organism:
Saccharomyces cerevisiae
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL19756
48 Samples
Download data: TAB
Series
Accession:
GSE83348
ID:
200083348
4.

Spatial regulation of transcription and histone occupancy by histone chaperones FACT and Spt6

(Submitter supplied) The FACT complex and Spt6 are conserved histone chaperones that are recruited to the open reading frames of transcribed genes. In this study, we provide evidence that FACT interaction with acetylated H3 tail is important for its localization to the coding sequences. Pol II CTD kinase Kin28 additionally stimulates FACT recruitment to a subset of genes. Pol II occupancies in the 5’ ends of transcribed genes are greatly reduced on depleting FACT, whereas reduced occupancies at the 3’ ends were observed upon Spt6 depletion indicating that these factors modulate Pol II progression through distinct regions of transcribed coding sequences. more...
Organism:
Saccharomyces cerevisiae
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL10930
28 Samples
Download data: TXT
Series
Accession:
GSE69642
ID:
200069642
5.

HDACs and Phosphorylated Pol II CTD recruit Spt6 for cotranscriptional histone reassembly

(Submitter supplied) Spt6 is a multifunctional histone chaperone involved in the maintenance of chromatin structure during elongation by RNA polymerase II (Pol II). Spt6 has a tandem SH2 (tSH2) domain within its C-terminus that recognizes Pol II CTD peptides phosphorylated on Ser2, Ser5 or Try1 in vitro. Deleting the tSH2 domain, however, only has a partial effect on Spt6 occupancy in vivo, suggesting that more complex mechanisms are involved in the Spt6 recruitment. more...
Organism:
Saccharomyces cerevisiae
Type:
Genome binding/occupancy profiling by genome tiling array; Expression profiling by RT-PCR
Platform:
GPL18340
28 Samples
Download data: BED, GPR
Series
Accession:
GSE61713
ID:
200061713
6.

Post-Transcriptional Role for the Yeast Paf1-RNA Polymerase II Complex is Revealed by Identification of Primary Targets

(Submitter supplied) To identify the direct targets of the Paf1/RNA polymerase II complex we compared expression profiles of isogenic wild type and paf1 and ctr9 mutant strains. We also created a Tet-regulated form of Paf1 and monitored expression patterns after shut off of Paf1. Samples were isolated at one hour intervals from 1 to 8 hours after shut off. Keywords: single channel nucleotide
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by array
Datasets:
GDS1550 GDS1551
Platform:
GPL90
11 Samples
Download data
Series
Accession:
GSE3200
ID:
200003200
7.
Full record GDS1551

paf1 and ctr9 null mutants

Expression profiling of paf1 and ctr9 null mutants. Paf1p and Ctr9p are part of the Paf1 complex (Paf1C) of RNA polymerase II associated proteins. Results provide insight into the role of Paf1C in gene expression.
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by array, count, 3 genotype/variation sets
Platform:
GPL90
Series:
GSE3200
5 Samples
Download data
DataSet
Accession:
GDS1551
ID:
1551
8.
Full record GDS1550

RNA polymerase II associated protein Paf1 depletion: time course

Analysis of cells depleted of Paf1, an RNA polymerase II associated protein. Cells were examined at various time points up to 8 hours following the inactivation of Paf1 expression from a tetracycline-regulated promoter using doxycyline (DOX). Results identify the primary targets of Paf1.
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by array, count, 2 agent, 6 time sets
Platform:
GPL90
Series:
GSE3200
6 Samples
Download data
DataSet
Accession:
GDS1550
ID:
1550
9.

Spt6 association with RNAPII directs mRNA turnover during transcription

(Submitter supplied) Spt6 is an essential histone chaperone that mediates nucleosome reassembly during gene transcription. Spt6 interacts with elongating RNA polymerase II (RNAPII) via a tandem Src2 homology (tSH2) domain, but it is not known whether this particular interaction is required for the nucleosome reassembly activity of Spt6. Here, we show that Spt6 recruitment to genes and its nucleosome reassembly functions are largely independent of association with RNAPII. more...
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL17342
12 Samples
Download data: BW, TXT
Series
Accession:
GSE111815
ID:
200111815
10.

The histone chaperone Spt6 is required for normal recruitment of the capping enzyme Abd1 to transcribed regions

(Submitter supplied) The histone chaperone Spt6 is involved in promoting elongation of RNA polymerase II (RNAPII), maintaining chromatin structure, regulating co-transcriptional histone modifications, and controlling mRNA processing. These diverse functions of Spt6 are partly mediated through its interactions with RNAPII and other factors in the transcription elongation complex. In this study, we used mass spectrometry to characterize the differences in RNAPII interacting factors between wild-type cells and those depleted for Spt6, leading to the identification of proteins that depend on Spt6 for their interaction with RNAPII. more...
Organism:
Saccharomyces cerevisiae
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL19756
24 Samples
Download data: BEDGRAPH
Series
Accession:
GSE171953
ID:
200171953
11.

Chromatin regulates alternative polyadenylation via the RNA polymerase II elongation rate

(Submitter supplied) The Pol II elongation rate influences poly(A) site selection, with slow and fast Pol II derivatives causing upstream and downstream shifts, respectively, in poly(A) site utilization. In yeast, depletion of either of the histone chaperones FACT or Spt6 causes an upstream shift of poly(A) site use that strongly resembles the poly(A) profiles of slow Pol II mutant strains. Like slow Pol II mutant strains, Spt6- and FACT-depleted cells exhibit processivity defects, indicating that both Spt6 and FACT stimulate the Pol II elongation rate. more...
Organism:
Saccharomyces cerevisiae
Type:
Other
Platform:
GPL19756
26 Samples
Download data: TXT
Series
Accession:
GSE262747
ID:
200262747
12.

The transcriptional elongation rate regulates alternative polyadenylation in yeast

(Submitter supplied) Yeast cells undergoing the diauxic response show a striking upstream shift in poly(A) site utilization, with increased use of ORF-proximal poly(A) sites resulting in shorter 3’ mRNA isoforms for most genes. This altered poly(A) pattern is extremely similar to that observed in cells containing Pol II derivatives with slow elongation rates. Conversely, cells containing derivatives with fast elongation rates show a subtle downstream shift in poly(A) sites. more...
Organism:
Saccharomyces cerevisiae
Type:
Other
Platform:
GPL19756
22 Samples
Download data: TXT
Series
Accession:
GSE151196
ID:
200151196
13.

Global analysis of mRNA isoform half-lives: identification of stabilizing and destabilizing elements in yeast

(Submitter supplied) We measured half-lives of 21,248 mRNA 3’ isoforms in yeast by rapidly depleting RNA polymerase II from the nucleus and performing direct RNA sequencing throughout the decay process. Interestingly, the half-lives of mRNA isoforms from the same gene, including nearly identical isoforms, often vary widely. Based on clusters of isoforms with different half-lives, we identify hundreds of sequences conferring stabilization or destabilization upon mRNAs terminating downstream. more...
Organism:
Saccharomyces cerevisiae
Type:
Other
Platform:
GPL17245
16 Samples
Download data: TXT
Series
Accession:
GSE52286
ID:
200052286
14.

SPT6 functions in transcriptional pause-release via PAF1C recruitment

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing
Platforms:
GPL18573 GPL24676
78 Samples
Download data: BW
Series
Accession:
GSE202190
ID:
200202190
15.

SPT6 functions in transcriptional pause-release via PAF1C recruitment [RNA-seq]

(Submitter supplied) In vitro studies identified various factors including P-TEFb, SEC, SPT6, PAF1, DSIF, and NELF functioning at different stages of transcription elongation driven by RNA polymerase II (RNA Pol II). What remains unclear is how these factors cooperatively regulate pause/release and productive elongation in the context of living cells. Using an acute protein-depletion approach, we report that SPT6 depletion results in release of paused RNA Pol II. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24676
12 Samples
Download data: CSV
Series
Accession:
GSE202189
ID:
200202189
16.

SPT6 functions in transcriptional pause-release via PAF1C recruitment [PRO-seq]

(Submitter supplied) In vitro studies identified various factors including P-TEFb, SEC, SPT6, PAF1, DSIF, and NELF functioning at different stages of transcription elongation driven by RNA polymerase II (RNA Pol II). What remains unclear is how these factors cooperatively regulate pause/release and productive elongation in the context of living cells. Using an acute protein-depletion approach, we report that SPT6 depletion results in release of paused RNA Pol II. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL18573 GPL24676
16 Samples
Download data: BW
Series
Accession:
GSE202187
ID:
200202187
17.

SPT6 functions in transcriptional pause-release via PAF1C recruitment [ChIP-seq]

(Submitter supplied) In vitro studies identified various factors including P-TEFb, SEC, SPT6, PAF1, DSIF, and NELF functioning at different stages of transcription elongation driven by RNA polymerase II (RNA Pol II). What remains unclear is how these factors cooperatively regulate pause/release and productive elongation in the context of living cells. Using an acute protein-depletion approach, we report that SPT6 depletion results in release of paused RNA Pol II. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL24676
50 Samples
Download data: BED, BW
Series
Accession:
GSE202184
ID:
200202184
18.

RTF1 and SPT6 stimulate transcription elongation by two distinct mechanisms

(Submitter supplied) We have previously shown that the RNA polymerase II (Pol II)-DSIF complex associates with the PAF1 complex (PAF), RTF1 and SPT6 to form an activated elongation complex in vitro. Here we investigate the mechanisms that these factors use to stimulate Pol II elongation in vivo. We combine rapid factor depletion from human cells with genome-wide analyses of changes in RNA synthesis and occupancy with engaged Pol II. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Other; Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL21697
47 Samples
Download data: BIGWIG, BW
19.

Spt6 is required for the fidelity of promoter selectivity

(Submitter supplied) Spt6 is a conserved factor that controls transcription and chromatin structure across the genome. Although viewed as an elongation factor, spt6 mutations allow transcription from within coding regions, suggesting that Spt6 also controls initiation. To comprehensively characterize the requirement for Spt6 in transcription, we have used four approaches: TSS-seq and TFIIB ChIP-nexus to assay transcription initiation, NET-seq to assay elongating RNAPII, and MNase-seq to assay nucleosome occupancy and positioning. more...
Organism:
Saccharomyces cerevisiae
Type:
Genome binding/occupancy profiling by high throughput sequencing; Other
Platforms:
GPL13821 GPL19756 GPL17143
21 Samples
Download data: BW
Series
Accession:
GSE115775
ID:
200115775
20.

The interaction between the Spt6-tSH2 domain and Rpb1 affects multiple functions of RNA Polymerase II [MNase-seq]

(Submitter supplied) The conserved transcription elongation factor Spt6 makes several contacts with the RNA Polymerase II (RNAPII) complex, including a high-affinity interaction between the Spt6 tandem SH2 domain (Spt6-tSH2) and phosphorylated residues of the Rpb1 subunit in the linker between the catalytic core and the C-terminal domain (CTD) heptad repeats. This interaction contributes to generic localization of Spt6, but we show here that it also has gene-specific roles. more...
Organism:
Saccharomyces cerevisiae
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL27812
6 Samples
Download data: BW
Series
Accession:
GSE189831
ID:
200189831
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