GEO DataSets

(Submitter supplied) Transcriptional profiling of C. lusitaniae a and alpha cells mixed on 0.37% PDA (potato dextrose agar) for 0 hours (h) ,4h, and 12n hybridized against WT cells on YPD for 4 hours and also a and alpha ime2 deletion mutants mixed on 0.37% PDA for 4 hours hybridized against WT cells on YPD (yeast peptone dextrose) for 4h

Organism:

Clavispora lusitaniae; Clavispora lusitaniae ATCC 42720

Type:

Expression profiling by array

Platform:

GPL17847

12 Samples

Download data: GPR

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.

Organism:

Clavispora lusitaniae; Clavispora lusitaniae ATCC 42720

Type:

Expression profiling by array

Platform:

GPL17847

70 Samples

Download data: GPR

(Submitter supplied) Transcriptional profiling of C. lusitaniae a/alpha WT cells on 0.37% PDA (potato dextrose agar) for 30 minutes (m), 2 hours (h), 4h, 8h, 12h, 18h, 24, and 30h hybridized against WT a/alpha cells in non-meiosis inducing conditions YPD (yeast peptone dextrose) for 2h

Organism:

Clavispora lusitaniae; Clavispora lusitaniae ATCC 42720

Type:

Expression profiling by array

Platform:

GPL17847

32 Samples

Download data: GPR

(Submitter supplied) Transcriptional profiling of C. lusitaniae a/alpha ste12Δ/ste12Δ deletion mutants on .37% PDA (potato dextrose agar) media for 0 hours (h), 12h, 28h, and 24 hours hybridized against WT a/alpha cells on YPD (yeast peptone dextrose) media for 2h

Organism:

Clavispora lusitaniae ATCC 42720; Clavispora lusitaniae

Type:

Expression profiling by array

Platform:

GPL17847

4 Samples

Download data: GPR

(Submitter supplied) Transcriptional profiling of C. lusitaniae WT a and WT alpha cells on 0.37% PDA (potato dextrose agar) for 30 minutes (m), 2 hours (h), or 24h hybridized against WT a and WT alpha cells in YPD (yeast peptone dextrose) for 2h

Organism:

Clavispora lusitaniae; Clavispora lusitaniae ATCC 42720

Type:

Expression profiling by array

Platform:

GPL17847

10 Samples

Download data: GPR

(Submitter supplied) Transcriptional profiling of C. lusitaniae ime2Δ/ime2Δ a/alpha WT cells on 0.37% PDA (potato dextrose agar) for 0 hours, 12h, 18h and 24h hybridized against WT a/alpha cells in YPD (yeast peptone dextrose) for 4h

Organism:

Clavispora lusitaniae; Clavispora lusitaniae ATCC 42720

Type:

Expression profiling by array

Platform:

GPL17847

12 Samples

Download data: GPR

(Submitter supplied) ChIP-chip to determine the regulation of the K. lactis hsgs (ChIP of MATa1, MATalpha2, and RME1). The MATa1 and MATalpha2 ChIPs were performed in an a/alpha cell using N-terminally HA-tagged proteins and the RME1 ChIPs were perfomed in an a cell using C-terminally myc-tagged protein. For the RME1 ChIPs, the cells grown with out phosphate. For the MATa1 andMATalpha2 ChIPs the cells were grown in YEPD.

Organism:

Kluyveromyces lactis NRRL Y-1140; Kluyveromyces lactis

Type:

Genome binding/occupancy profiling by genome tiling array

Platform:

GPL11182

6 Samples

Download data: GPR

(Submitter supplied) WT and rme1 KO K. lactis cells (a, alpha, and a/alpha) were grown in YEPD, phosphate starvation and phosphate starvation with the addition of alpha pheromone. The goal was to identify cell-type regulated genes and to determine the effects of growth media on the regulation of cell-type regulated genes

Organism:

Kluyveromyces lactis

Type:

Expression profiling by array

Platform:

GPL10962

20 Samples

Download data: GPR

(Submitter supplied) Twenty-one pheromone-induced genes were selected from the literature (Zhao, Daniels et al. 2005 was the major source) as the reference set for assessing the pheromone response of CAI4 (Wild-type), cpp1Δ/Δ, cek1Δ/Δ, cek2Δ/Δ, cpp1Δ/Δ cek1Δ/Δ, cpp1Δ/Δ cek2Δ/Δ and cek1Δ/Δ cek2Δ/Δ strains.Our aim was to check whether or not these 21 pheromone-induced genes are up-regulated in response to pheromone in each mutant strain.

Organism:

Candida albicans

Type:

Expression profiling by high throughput sequencing

Platform:

GPL23041

28 Samples

Download data: TSV, XLSX

(Submitter supplied) Modes of sexual reproduction in eukaryotic organisms are highly diversified. The human fungal pathogen Candida albicans undergoes a phenotypic switch from the white to the opaque phase in order to become mating-competent. In this study, we report that functionally and morphologically differentiated white and opaque cells show a coordinating behavior in the process of mating. Although white cells are mating-incompetent, they are induced to produce sexual pheromones when treated with opposite pheromones or interacted with opaque cells of an opposite mating type. more...

Organism:

Candida albicans

Type:

Expression profiling by high throughput sequencing

Platform:

GPL15645

2 Samples

Download data: TXT

(Submitter supplied) The different expression of Candida glabrata haploid and diploid.

Organism:

Nakaseomyces glabratus

Type:

Expression profiling by high throughput sequencing

Platform:

GPL30061

6 Samples

Download data: TXT

(Submitter supplied) Sexual reproduction facilitates infection by the production of both a lineage advantage and infectious sexual spores in the ubiquitous human fungal pathogen Cryptococcus deneoformans. However, the regulatory determinants specific for initiating mating remain poorly understood. Here, we identified a velvet family regulator, Cva1, that strongly promotes sexual reproduction in C. deneoformans. This regulation was determined to be specific, based on a comprehensive phenotypic analysis of cva1 under 25 distinct in vitro and in vivo growth conditions. more...

Organism:

Cryptococcus neoformans var. neoformans XL280

Type:

Expression profiling by high throughput sequencing

Platform:

GPL24742

4 Samples

Download data: XLSX

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.

Organism:

Lachancea kluyveri

Type:

Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing

Platform:

GPL32984

25 Samples

Download data: BW

(Submitter supplied) Over evolutionary timescales, the logic and pattern of cell-type specific gene expression can remain constant, yet the molecular mechanisms underlying such regulation can drift between alternative forms. Here, we document a new, especially clear example of this principle in the regulation of the haploid-specific genes across a wide group of fungal species. For most species, transcription of these genes is repressed in the a/ a cell type by a heterodimer of two homeodomain proteins, Mata1 and Mata2. more...

Organism:

Lachancea kluyveri

Type:

Expression profiling by high throughput sequencing

Platform:

GPL32984

9 Samples

Download data: CSV, TXT

(Submitter supplied) Over evolutionary timescales, the logic and pattern of cell-type specific gene expression can remain constant, yet the molecular mechanisms underlying such regulation can drift between alternative forms. Here, we document a new, especially clear example of this principle in the regulation of the haploid-specific genes across a wide group of fungal species. For most species, transcription of these genes is repressed in the a/ a cell type by a heterodimer of two homeodomain proteins, Mata1 and Mata2. more...

Organism:

Lachancea kluyveri

Type:

Genome binding/occupancy profiling by high throughput sequencing

Platform:

GPL32984

16 Samples

Download data: BW