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Links from GEO DataSets

Items: 11

1.

Unmethylated Cyc1 downregulates hyphal specific genes and upregulates hyphal suppressors in Candida albicans

(Submitter supplied) Our genetic screen reveals that deletion of CTM1, which abolishes the lysine trimethylation of cytochrome c (Cyc1), results in inhibition of hyphal morphogenesis in Candida albicans. Similar results are observed in the unmethylatable Cyc1 mutant (cyc1K79A). To elucidate how unmethylated Cyc1 inhibits hyphal growth, we performed RNA-Seq analysis by comparing WT (BWP17), ctm1∆/∆, and cyc1K79A cells grown in yeast and hyphal condition. more...
Organism:
Candida albicans SC5314
Type:
Expression profiling by high throughput sequencing
Platform:
GPL33780
27 Samples
Download data: XLSX
Series
Accession:
GSE243813
ID:
200243813
2.

A metabolic checkpoint controls hyphal development in Candida albicans via nitric oxide signaling

(Submitter supplied) We investigated the roles of mitochondrial dynamics in hyphal growth of C. albicans using the small molecule inhibitor MDIVI-1. Strikingly, the small molecule inhibitor represses both the yeast-to hyphae transition and ongoing filamentation, and its effects on morphogenesis can be uncoupled from general growth inhibition. RNAseq experiments of inhibitor-treated cells coupled with Candida mutant analyses suggest the existence of a novel mechanism of action to represses hyphal growth. more...
Organism:
Candida albicans
Type:
Expression profiling by high throughput sequencing
Platform:
GPL23573
28 Samples
Download data: CSV
Series
Accession:
GSE105148
ID:
200105148
3.

Integration of the tricarboxylic acid (TCA) cycle with cAMP signaling and Sfl2 pathways in the regulation of CO2 sensing, filamentation, and virulence in Candida albicans

(Submitter supplied) Candida albicans is the most common opportunistic fungal pathogen of humans and is also a benign member of the gastrointestinal (GI) tract microbiota. Morphological transitions and metabolic regulation are critical for C. albicans to adapt to the changing host environment. We generated a library of central metabolic pathway mutants in the tricarboxylic acid (TCA) cycle, and investigated the functional consequences of these gene deletions on C. more...
Organism:
Candida albicans
Type:
Expression profiling by high throughput sequencing
Platform:
GPL15645
8 Samples
Download data: XLS
Series
Accession:
GSE102039
ID:
200102039
4.

The Ndr/LATS kinase Cbk1 regulates a specific subset of Ace2 functions and suppresses the hyphae-to-yeast transition in Candida albicans

(Submitter supplied) The Regulation of Ace2 and Morphogenesis (RAM) pathway is an important regulatory network in the human fungal pathogen Candida albicans. The RAM pathway’s two most well-studied components, the NDR/Lats kinase Cbk1 and its putative substrate, the transcription factor Ace2, have a wide range of phenotypes and functions. It is not clear, however, which of these functions are specifically due to the phosphorylation of Ace2 by Cbk1. more...
Organism:
Candida albicans
Type:
Expression profiling by high throughput sequencing
Platform:
GPL28323
18 Samples
Download data: CSV, XLSX
Series
Accession:
GSE155450
ID:
200155450
5.

Functional Portrait of Irf1 (Orf19.217), a Regulator of Morphogenesis and Iron Homeostasis in Candida albicans

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Candida albicans
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL24725 GPL19036
24 Samples
Download data: BED
Series
Accession:
GSE207073
ID:
200207073
6.

Functional Portrait of Irf1 (Orf19.217), a Regulator of Morphogenesis and Iron Homeostasis in Candida albicans [RNA-Seq]

(Submitter supplied) The fungus Candida albicans is part of the human microbiome and mainly colonises the GI tract of healthy individuals. However, when the balance in the GI tract is disturbed, the fungus can switch from a commensal to a virulent lifestyle and can turn into a life-threatening pathogen. Life in the host is characterised by a constant struggle for nutrients, essential trace elements such as iron, copper and zinc are particularly important. more...
Organism:
Candida albicans
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19036
18 Samples
Download data: TXT
Series
Accession:
GSE207072
ID:
200207072
7.

Functional Portrait of Irf1 (Orf19.217), a Regulator of Morphogenesis and Iron Homeostasis in Candida albicans [ChIP-Seq]

(Submitter supplied) The fungus Candida albicans is part of the human microbiome and mainly colonises the GI tract of healthy individuals. However, when the balance in the GI tract is disturbed, the fungus can switch from a commensal to a virulent lifestyle and can turn into a life-threatening pathogen. Life in the host is characterised by a constant struggle for nutrients, essential trace elements such as iron, copper and zinc are particularly important. more...
Organism:
Candida albicans
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL24725
6 Samples
Download data: BED
Series
Accession:
GSE207033
ID:
200207033
8.

Transcriptomic and Metabolomic Analysis Revealed Roles of Yck2 in Carbon Metabolism and Morphogenesis of Candida albicans

(Submitter supplied) Candida albicans is a part of the normal microbiome of human mucosa and is able to thrive in a wide range of host environments. As an opportunistic pathogen, the virulence of C. albicans is tied to its ability to switch between yeast and hyphal morphologies in response to various environmental cues, one of which includes nutrient availability. Thus, metabolic flexibility plays an important role in the virulence of the pathogen. more...
Organism:
Candida albicans SC5314
Type:
Expression profiling by high throughput sequencing
Platform:
GPL27535
6 Samples
Download data: XLSX
Series
Accession:
GSE138069
ID:
200138069
9.

ChIP-Seq analysis of Candida albicans Sfl1p and Sfl2p

(Submitter supplied) Sfl1p and Sfl2p are two homologous heat shock factor-type transcriptional regulators that antagonistically control morphogenesis in Candida albicans, while being required for full pathogenesis and virulence. To understand how Sfl1p and Sfl2p exert their function, we combined genome-wide location and expression analyses to reveal their transcriptional targets in vivo together with the associated changes of the C. more...
Organism:
Candida albicans
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL15645
8 Samples
Download data: WIG
Series
Accession:
GSE42886
ID:
200042886
10.

Transcriptional profiling of Candida albicans cells defective in glucan assembly and undergoing the Yeast to Hyphal transition

(Submitter supplied) Wild type (CAI10) and phr1 null mutant (CAS10) were analyzed at 0, 1, 3 and 5 hours after the shift of blastospores to Hyphae inducing conditions
Organism:
Candida albicans
Type:
Expression profiling by array
Platform:
GPL9545
24 Samples
Download data: TXT
Series
Accession:
GSE51064
ID:
200051064
11.

A Genome-wide Transcriptional Analysis of Morphology Determination in Candida albicans

(Submitter supplied) Candida albicans, the most common cause of human fungal infections, undergoes a reversible morphological transition from yeast to pseudohyphal and hyphal filaments, which is required for virulence. For many years, the relationship between global gene expression patterns associated with determination of specific C. albicans morphologies has remained obscure. Using a strain that can be genetically manipulated to sequentially transition from yeast to pseudohyphae to hyphae in the absence of complex environmental cues and upstream signaling pathways, we demonstrate by whole-genome transcriptional profiling that genes associated with pseudohyphae represent a subset of those associated hyphae and are generally expressed at lower levels; interestingly, no genes appeared to be expressed exclusively in pseudohyphae. more...
Organism:
Candida albicans
Type:
Expression profiling by array
Platform:
GPL15843
136 Samples
Download data: CSV, GPR
Series
Accession:
GSE39677
ID:
200039677
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