U.S. flag

An official website of the United States government

Format
Items per page
Sort by

Send to:

Choose Destination

Links from GEO DataSets

Items: 18

1.

Yeast meiotic transcriptom kar4 delete v. wild type

(Submitter supplied) Transcriptional profiling of wild type and kar4 deletion yeast mutants across a meiotic time course. Including samples with IME1 and RIM4 overexpression
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by array
Platform:
GPL19008
175 Samples
Download data: TXT, XLSX
Series
Accession:
GSE220125
ID:
200220125
2.

Yeast meiotic transcriptional profile

(Submitter supplied) RNAseq across a time cours of meiosis of cells with and without Kar4p. The overexpression of either IME1 or both IME1 and RIM4 was used to determine how overexpression of the two genes functions to resuce the meiotic defect associated with the loss of Kar4p.
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by high throughput sequencing
Platform:
GPL27812
72 Samples
Download data: XLSX
Series
Accession:
GSE221451
ID:
200221451
3.

Yeast meiotic transcriptional profile [Kfc1p mutant]

(Submitter supplied) RNAseq across a time course of meiosis of cells with and without Kfc1p. The overexpression of either IME1 or both IME1 and RIM4 was used to determine how overexpression of the two genes functions to resuce the meiotic defect associated with the loss of Kar4p.
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by high throughput sequencing
Platform:
GPL27812
64 Samples
Download data: XLSX
Series
Accession:
GSE222684
ID:
200222684
4.

The Transcriptional Regulator Ume6 is a Major Driver of Gene Expression during Gametogenesis in Budding Yeast

(Submitter supplied) Early meiotic genes (EMGs) encompass an important subset within the developmental program of gametogenesis. Regulation of EMGs is achieved through the recognition of a common regulatory element in their promoters by the transcription factor Ume6. Proper meiotic execution requires the timely expression of EMGs, which is achieved through the adoption of the meiotic regulator Ime1 by Ume6. While it is known that Ime1’s binding to Ume6 promotes EMG expression, the mechanism of EMG activation remains unclear. more...
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by high throughput sequencing
Platform:
GPL27812
222 Samples
Download data: CSV
Series
Accession:
GSE226769
ID:
200226769
5.

LUTI-dependent Downregulation of a Cell Cycle Transcription Factor is Key for Timely Meiotic Entry

(Submitter supplied) We used RNA-seq to monitor expression of early meiotic genes and expression of mitotic transcription factor SBF targets. Increased SBF activity was achieved through either overexpression of SBF unique subunit Swi4 , removal of LUTI-mediated regulation of Swi4 levels, or nuclear depeletion of negative regulator of SBF Whi5.
Organism:
Saccharomyces cerevisiae SK1
Type:
Expression profiling by high throughput sequencing
Platform:
GPL33179
13 Samples
Download data: XLSX
Series
Accession:
GSE225963
ID:
200225963
6.

RNA-SEQ analysis of bdf1-Y187F-Y354F mutant strain during yeast sporulation

(Submitter supplied) The aim of this study is to compare NGS-derived yeast transcriptome profiling (RNA-seq) of wild-type and bdf1-Y187F-Y354F mutant strains after sporulation induction (time points: 0h 4h and 8h).
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13821
18 Samples
Download data: TXT
Series
Accession:
GSE89530
ID:
200089530
7.

The yeast RNA methylation complex consists of conserved yet reconfigured components with m6A-dependent and independent roles

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below. Abstract: N6-methyladenosine (m6A), the most abundant mRNA modification, is deposited in mammals/insects/plants by m6A methyltransferase complexes (MTC) comprising a catalytic subunit and at least five additional proteins. The yeast MTC is critical for meiosis and was known to comprise three proteins, of which two were conserved. We uncover three novel MTC components (Kar4/Ygl036w-Vir1/Dyn2). more...
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by high throughput sequencing; Other
Platforms:
GPL19756 GPL27812
215 Samples
Download data: RDS
Series
Accession:
GSE224836
ID:
200224836
8.

The yeast RNA methylation complex consists of conserved yet reconfigured components with m6A-dependent and independent roles [m6A-Seq]

(Submitter supplied) N6-methyladenosine (m6A), the most abundant mRNA modification, is deposited in mammals/insects/plants by m6A methyltransferase complexes (MTC) comprising a catalytic subunit and at least five additional proteins. The yeast MTC is critical for meiosis and was known to comprise three proteins, of which two were conserved. We uncover three novel MTC components (Kar4/Ygl036w-Vir1/Dyn2). All MTC subunits, except for Dyn2, are essential for m6A deposition and have corresponding mammalian MTC orthologs. more...
Organism:
Saccharomyces cerevisiae
Type:
Other
Platforms:
GPL27812 GPL19756
76 Samples
Download data: RDS
Series
Accession:
GSE224835
ID:
200224835
9.

The yeast RNA methylation complex consists of conserved yet reconfigured components with m6A-dependent and independent roles [RNA-Seq]

(Submitter supplied) N6-methyladenosine (m6A), the most abundant mRNA modification, is deposited in mammals/drosophila/plants by m6A methyltransferase complexes (MTC) comprising a catalytic subunit and at least five additional proteins. The yeast MTC is critical for meiosis but was known to comprise three proteins, of which two were conserved. We uncover three novel MTC components (Kar4/Ygl036w-Vir1/Dyn2). All MTC subunits, except for Dyn2, are essential for m6A deposition and have corresponding mammalian MTC orthologs. more...
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by high throughput sequencing
Platform:
GPL27812
139 Samples
Download data: BED, TAB
Series
Accession:
GSE224833
ID:
200224833
10.

The S. cerevisiae m6A reader Pho92 promotes timely meiotic recombination by controlling key methylated transcripts.

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL19756 GPL21656
71 Samples
Download data: BW
Series
Accession:
GSE200089
ID:
200200089
11.

The S. cerevisiae m6A reader Pho92 promotes timely meiotic recombination by controlling key methylated transcripts [CRAC]

(Submitter supplied) We performed CRAC (UV-crosslinking and analysis of cDNA) to identify Ime4-dependent mRNA targets of Pho92 during meiosis at 5 hr in SPO.
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19756
8 Samples
Download data: BW, XLSX
Series
Accession:
GSE200088
ID:
200200088
12.

The S. cerevisiae m6A reader Pho92 promotes timely meiotic recombination by controlling key methylated transcripts [RNA-seq]

(Submitter supplied) We performed high-throughput mRNA sequencing during a meiotic time course (0, 2, 3, 5, 6, 7 and 9 hr) in WT, pho92 mutant and ime4 mutant cells.
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21656
63 Samples
Download data: XLSX
Series
Accession:
GSE200087
ID:
200200087
13.

Effect of aging on the meiotic cell cycle

(Submitter supplied) Identify which stages of meiosis are impaired in replicative aging cells Transcriptional profile of aging yeast cells (young and old) incubated in sporulation-inducing conditions compared to new-born cells grown in vegetative conditions.
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by array
Platform:
GPL7259
4 Samples
Download data: TXT
Series
Accession:
GSE15570
ID:
200015570
14.

Transcription levels of a noncoding RNA orchestrate opposing regulatory and cell fate outcomes in yeast

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by high throughput sequencing; Other
Platforms:
GPL21656 GPL17342
30 Samples
Download data: BW
Series
Accession:
GSE138898
ID:
200138898
15.

Transcription levels of a long noncoding RNA shape a cell fate regulatory circuit (TES-seq)

(Submitter supplied) Long noncoding RNAs (lncRNA) play diverse roles in gene regulation controlling key cellular processes, most notably, cell-fate programming {Anderson, 2016 #20;Flynn, 2014 #16;Guttman, 2011 #35;Wang, 2011 #18}. Many long noncoding RNAs (lncRNAs) act in cis through transcription-coupled chromatin alterations that drive changes in local gene expression { Martens, 2004 #47; Kim, 2012 #74;van Werven, 2012 #57;Hainer, 2011 #73;Kim, 2016 #41;Ard, 2016 #21;Latos, 2012 #7}. more...
Organism:
Saccharomyces cerevisiae
Type:
Other
Platform:
GPL21656
8 Samples
Download data: BW
Series
Accession:
GSE138897
ID:
200138897
16.

Transcription levels of a long noncoding RNA shape a cell fate regulatory circuit (TSS-seq)

(Submitter supplied) Long noncoding RNAs (lncRNA) play diverse roles in gene regulation controlling key cellular processes, most notably, cell-fate programming {Anderson, 2016 #20;Flynn, 2014 #16;Guttman, 2011 #35;Wang, 2011 #18}. Many long noncoding RNAs (lncRNAs) act in cis through transcription-coupled chromatin alterations that drive changes in local gene expression { Martens, 2004 #47; Kim, 2012 #74;van Werven, 2012 #57;Hainer, 2011 #73;Kim, 2016 #41;Ard, 2016 #21;Latos, 2012 #7}. more...
Organism:
Saccharomyces cerevisiae
Type:
Other
Platform:
GPL21656
8 Samples
Download data: BW
Series
Accession:
GSE138896
ID:
200138896
17.

Transcription levels of a long noncoding RNA shape a cell fate regulatory circuit (PolII associated RNA-seq)

(Submitter supplied) Long noncoding RNAs (lncRNA) play diverse roles in gene regulation controlling key cellular processes, most notably, cell-fate programming {Anderson, 2016 #20;Flynn, 2014 #16;Guttman, 2011 #35;Wang, 2011 #18}. Many long noncoding RNAs (lncRNAs) act in cis through transcription-coupled chromatin alterations that drive changes in local gene expression { Martens, 2004 #47; Kim, 2012 #74;van Werven, 2012 #57;Hainer, 2011 #73;Kim, 2016 #41;Ard, 2016 #21;Latos, 2012 #7}. more...
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21656
6 Samples
Download data: BW
Series
Accession:
GSE138895
ID:
200138895
18.

Transcription levels of a long noncoding RNA shape a cell fate regulatory circuit (mRNA-seq)

(Submitter supplied) Long noncoding RNAs (lncRNA) play diverse roles in gene regulation controlling key cellular processes, most notably, cell-fate programming {Anderson, 2016 #20;Flynn, 2014 #16;Guttman, 2011 #35;Wang, 2011 #18}. Many long noncoding RNAs (lncRNAs) act in cis through transcription-coupled chromatin alterations that drive changes in local gene expression { Martens, 2004 #47; Kim, 2012 #74;van Werven, 2012 #57;Hainer, 2011 #73;Kim, 2016 #41;Ard, 2016 #21;Latos, 2012 #7}. more...
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL17342 GPL21656
8 Samples
Download data: BW
Series
Accession:
GSE138893
ID:
200138893
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

db=gds|term=|query=1|qty=3|blobid=MCID_663e1aebb0dc3a4c1e59d959|ismultiple=true|min_list=5|max_list=20|def_tree=20|def_list=|def_view=|url=/Taxonomy/backend/subset.cgi?|trace_url=/stat?
   Taxonomic Groups  [List]
Tree placeholder
    Top Organisms  [Tree]

Find related data

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...
Support Center