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Links from GEO DataSets

Items: 20

1.

Quantitative BrdU immunoprecipitation method demonstrates that Fkh1 and Fkh2 are rate-limiting activators of replication origins that reprogram replication timing in G1 phase (BrdU)

(Submitter supplied) The S. cerevisiae Forkhead Box (FOX) proteins, Fkh1 and Fkh2, regulate diverse cellular processes including transcription, long-range DNA interactions during homologous recombination, and replication origin timing and long-range origin clustering. As stimulators of early origin activation, we hypothesized that Fkh1 and Fkh2 abundance limits the rate of origin activation genome-wide. Existing methods, however, were not well suited to quantitative, genome-wide measurements of origin firing between strains and conditions. more...
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by high throughput sequencing; Other
Platform:
GPL19756
64 Samples
Download data: TXT
Series
Accession:
GSE71050
ID:
200071050
2.

Quantitative BrdU immunoprecipitation method demonstrates that Fkh1 and Fkh2 are rate-limiting activators of replication origins that reprogram replication timing in G1 phase

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by high throughput sequencing; Other; Genome binding/occupancy profiling by array
Platforms:
GPL19756 GPL14887
70 Samples
Download data: PAIR
Series
Accession:
GSE71052
ID:
200071052
3.

Quantitative BrdU immunoprecipitation method demonstrates that Fkh1 and Fkh2 are rate-limiting activators of replication origins that reprogram replication timing in G1 phase (ChIP)

(Submitter supplied) The S. cerevisiae Forkhead Box (FOX) proteins, Fkh1 and Fkh2, regulate diverse cellular processes including transcription, long-range DNA interactions during homologous recombination, and replication origin timing and long-range origin clustering. As stimulators of early origin activation, we hypothesized that Fkh1 and Fkh2 abundance limits the rate of origin activation genome-wide. Existing methods, however, were not well suited to quantitative, genome-wide measurements of origin firing between strains and conditions. more...
Organism:
Saccharomyces cerevisiae
Type:
Genome binding/occupancy profiling by array
Platform:
GPL14887
6 Samples
Download data: PAIR
Series
Accession:
GSE71051
ID:
200071051
4.

Conserved forkhead dimerization motif controls DNA replication timing and spatial organization of chromosomes in S. cerevisiae

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Saccharomyces cerevisiae
Type:
Genome binding/occupancy profiling by genome tiling array; Other
Platforms:
GPL14887 GPL13821
28 Samples
Download data: BED, PAIR, WIG
Series
Accession:
GSE94796
ID:
200094796
5.

Conserved forkhead dimerization motif controls DNA replication timing and spatial organization of chromosomes in S. cerevisiae (HTS)

(Submitter supplied) Forkhead Box (Fox) proteins share the Forkhead domain, a winged-helix DNA binding module, which is conserved among eukaryotes from yeast to humans. These sequence-specific DNA binding proteins have been primarily characterized as transcription factors regulating diverse cellular processes from cell cycle control to developmental fate, deregulation of which contributes to developmental defects, cancer, and aging. more...
Organism:
Saccharomyces cerevisiae
Type:
Other
Platform:
GPL13821
22 Samples
Download data: BED
Series
Accession:
GSE94795
ID:
200094795
6.

Conserved forkhead dimerization motif controls DNA replication timing and spatial organization of chromosomes in S. cerevisiae (ChIP-chip)

(Submitter supplied) Forkhead Box (Fox) proteins share the Forkhead domain, a winged-helix DNA binding module, which is conserved among eukaryotes from yeast to humans. These sequence-specific DNA binding proteins have been primarily characterized as transcription factors regulating diverse cellular processes from cell cycle control to developmental fate, deregulation of which contributes to developmental defects, cancer, and aging. more...
Organism:
Saccharomyces cerevisiae
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL14887
6 Samples
Download data: PAIR, WIG
Series
Accession:
GSE93518
ID:
200093518
7.

Fkh1 and Fkh2 Bind Multiple Chromosomal Elements in the S. cerevisiae Genome with Distinct Specificities and Cell Cycle Dynamics

(Submitter supplied) Forkhead box (FOX) transcription factors regulate a wide variety of cellular functions in higher eukaryotes, including cell cycle control and developmental regulation. In Saccharomyces cerevisiae, Forkhead proteins Fkh1 and Fkh2 perform analogous functions, regulating genes involved in cell cycle control, while also regulating matingtype silencing and switching involved in gamete development. Recently, we revealed a novel role for Fkh1 and Fkh2 in the regulation of replication origin initiation timing, which, like donor preference in mating-type switching, appears to involve long-range chromosomal interactions, suggesting roles for Fkh1 and Fkh2 in chromatin architecture and organization. more...
Organism:
Saccharomyces cerevisiae
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL14887
30 Samples
Download data: PAIR
Series
Accession:
GSE52467
ID:
200052467
8.

Forkhead transcription factors establish origin timing and long-range clustering in S. cerevisiae

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing; Genome binding/occupancy profiling by genome tiling array
Platforms:
GPL9377 GPL14887
56 Samples
Download data: PAIR
Series
Accession:
GSE33704
ID:
200033704
9.

Forkhead transcription factors establish origin timing and long-range clustering in S. cerevisiae [Array Data]

(Submitter supplied) The replication of eukaryotic chromosomes is organized temporally and spatially within the nucleus through epigenetic regulation of replication origin function. The characteristic initiation timing of specific origins is thought to reflect their chromatin environment or sub-nuclear positioning, however the mechanism remains obscure. Here we show that the yeast Forkhead transcription factors, Fkh1 and Fkh2, are global determinants of replication origin timing. more...
Organism:
Saccharomyces cerevisiae
Type:
Genome binding/occupancy profiling by genome tiling array; Other
Platform:
GPL14887
30 Samples
Download data: PAIR
Series
Accession:
GSE33702
ID:
200033702
10.

Forkhead transcription factors establish origin timing and long-range clustering in S. cerevisiae [Sequence Data]

(Submitter supplied) The replication of eukaryotic chromosomes is organized temporally and spatially within the nucleus through epigenetic regulation of replication origin function. The characteristic initiation timing of specific origins is thought to reflect their chromatin environment or sub-nuclear positioning, however the mechanism remains obscure. Here we show that the yeast Forkhead transcription factors, Fkh1 and Fkh2, are global determinants of replication origin timing. more...
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL9377
26 Samples
Download data: TXT
Series
Accession:
GSE33677
ID:
200033677
11.

Rpd3 regulates single-copy origins independently of the rDNA array by opposing origin stimulation by Fkh1 [BrdU-IP-seq]

(Submitter supplied) The replication of eukaryotic genomes is highly regulated to ensure faithful transmission of all genetic information through cell divisions. In addition to stringent control of origin initiation by cell cycle controls and DNA damage checkpoints, spatial and temporal control of origins serves to stage and balance replication of different genomic regions, with potential implications for development and genome stability. more...
Organism:
Saccharomyces cerevisiae
Type:
Other
Platform:
GPL27812
48 Samples
Download data: BED
Series
Accession:
GSE200349
ID:
200200349
12.

Dbf4 recruitment by forkhead transcription factors defines an upstream rate-limiting step in determining replication origin firing

(Submitter supplied) Initiation of eukaryotic chromosome replication follows a spatiotemporal program. Current model suggests that replication origins compete for a limited pool of initiation factors. However, it remains to be answered how these limiting factors are preferentially recruited to early origins. Here, we report that Dbf4 is enriched at early origins through its interaction with forkhead transcription factors Fkh1 and Fkh2. more...
Organism:
Saccharomyces cerevisiae
Type:
Other
Platforms:
GPL13821 GPL21656
13 Samples
Download data: BIGWIG
Series
Accession:
GSE103073
ID:
200103073
13.

Rif1 regulates initiation timing of late replication origins throughout the S. cerevisiae genome

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Saccharomyces cerevisiae
Type:
Other
Platforms:
GPL14887 GPL13821
34 Samples
Download data: PAIR
Series
Accession:
GSE55156
ID:
200055156
14.

Rif1 regulates initiation timing of late replication origins throughout the S. cerevisiae genome [ChIP-Seq]

(Submitter supplied) Chromosomal DNA replication involves the coordinated activity of hundreds to thousands of replication origins. Individual replication origins are subject to epigenetic regulation of their activity during S-phase, resulting in differential efficiencies and timings of replication initiation during S-phase. This regulation is thought to involve chromatin structure and organization into timing domains with differential ability to recruit limiting replication factors. more...
Organism:
Saccharomyces cerevisiae
Type:
Other
Platform:
GPL13821
4 Samples
Download data: TXT
Series
Accession:
GSE55155
ID:
200055155
15.

Rif1 regulates initiation timing of late replication origins throughout the S. cerevisiae genome [array]

(Submitter supplied) Chromosomal DNA replication involves the coordinated activity of hundreds to thousands of replication origins. Individual replication origins are subject to epigenetic regulation of their activity during S-phase, resulting in differential efficiencies and timings of replication initiation during S-phase. This regulation is thought to involve chromatin structure and organization into timing domains with differential ability to recruit limiting replication factors. more...
Organism:
Saccharomyces cerevisiae
Type:
Other
Platform:
GPL14887
30 Samples
Download data: PAIR
Series
Accession:
GSE55130
ID:
200055130
16.

Dbf4 Zn-finger motif is specifically required for stimulation of Ctf19-activated origins in S. cerevisiae

(Submitter supplied) Eukaryotic genomes are replicated in spatiotemporal patterns that are stereotypical for individual genomes and developmental profiles. In the model system S. cerevisiae, two primary mechanisms determine the preferential activation of replication origins during early S phase, thereby largely defining the consequent replication profiles of these cells. Both mechanisms are thought to act through specific recruitment of a rate-limiting initiation factor, Dbf4-dependent kinase (DDK), to a subset of licensed replication origins. more...
Organism:
Saccharomyces cerevisiae
Type:
Other; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL26302 GPL27812
44 Samples
Download data: BED
Series
Accession:
GSE215190
ID:
200215190
17.

MRC1-Dependent Scaling of the Budding Yeast DNA Replication Timing Program

(Submitter supplied) Fourteen yeast mutants with an extended S-phase were identified by a novel genome-wide screen. These mutants are associated with the DNA replication machinery, cell-cycle control and dNTP synthesis. We determined the genome-wide DNA replication timing profile of all these mutants as well as wild type, by FACS-sorting G1- and S-phase cells and co-hybridizing their DNA to Agilent genomic tiling arrays, in four repeats each. more...
Organism:
Saccharomyces cerevisiae
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL4131
58 Samples
Download data: SRR, TXT
Series
Accession:
GSE17120
ID:
200017120
18.

Different nucleosomal landscapes at early and late replicating origins in Saccharomyces cerevisiae

(Submitter supplied) Sequencing of mononucleosomal DNA during G1 and S phases in Saccharomyces cerevisiae
Organism:
Saccharomyces cerevisiae
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL13272
4 Samples
Download data: WIG
Series
Accession:
GSE54377
ID:
200054377
19.

Time series data of chromatin and transcription throughout the cell cycle

(Submitter supplied) The occupancy states of DNA-binding nucleosomes and subnucleosome-sized proteins (e.g.  transcription factors, replication proteins, etc.) determine the chromatin accessibility landscape and provide additional regulatory context for DNA-templated processes including transcription and DNA replication. Throughout the mitotic cell division cycles, the transcriptome undergoes periodic reprogramming along with replication- and mitosis-induced global chromatin reconfiguration; however, profiling of the cell cycle-specific chromatin dynamics and understandings of its regulatory mechanisms remain limited. more...
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL19756
59 Samples
Download data: CSV
Series
Accession:
GSE168699
ID:
200168699
20.

Nucleosome occupancy as a novel chromatin parameter for replication origin functions

(Submitter supplied) This study defines nucleosome occupancy as a novel parameter for regulating origin activities. Nucleosome occupancy at origins was assessed using histone H3 ChIP-seq during G1 and G2M. Origin activity was determined using BrdU ChIP-seq.
Organism:
Saccharomyces cerevisiae
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL9134
37 Samples
Download data: SGR
Series
Accession:
GSE81028
ID:
200081028
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Supplemental Content

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