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Links from GEO DataSets

Items: 14

1.

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
2.

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
3.

Conjugated linoleic acid inhibits hyphal growth in Candida albicans by modulating Ras1 cellular levels and down-regulating TEC1 expression

(Submitter supplied) The polymorphic yeast Candida albicans exists in blastospore and filamentous forms. The switch from one morphological state to the other coincides with the expression of virulence factors, which makes the yeast-to-hypha transition an attractive target for the development of new antifungal agents. Because an untapped therapeutic potential resides in small molecules that hinder C. albicans filamentation, we characterized the inhibitory effect of conjugated linoleic acid (CLA) on hyphal growth and addressed its mechanism of action. more...
Organism:
Candida albicans
Type:
Expression profiling by array
Platform:
GPL9818
12 Samples
Download data: TXT
Series
Accession:
GSE25822
ID:
200025822
4.

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
5.

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
6.

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
7.

The protein kinase Tor1 regulates adhesin expression in Candida albicans

(Submitter supplied) Eukaryotic cell growth is coordinated in response to nutrient availability, growth factors, and environmental stimuli, enabling cell–cell interactions that promote survival. The rapamycin-sensitive Tor1 protein kinase, which is conserved from yeasts to humans, participates in a signaling pathway central to cellular nutrient responses. To gain insight into Tor-mediated processes in human fungal pathogens, we have characterized Tor signaling in Candida albicans. more...
Organism:
Candida albicans
Type:
Expression profiling by array
Platform:
GPL7476
12 Samples
Download data: GPR
Series
Accession:
GSE13176
ID:
200013176
8.

Cell cycle-independent phospho-regulation of Fkh2 during hyphal growth regulates Candida albicans pathogenesis.

(Submitter supplied) The opportunistic human fungal pathogen, Candida albicans, undergoes morphological and transcriptional adaptation in the switch from commensalism to pathogenicity. Although previous gene-knockout studies have identified many factors involved in this transformation, it remains unclear how these factors are regulated to coordinate the switch. Investigating morphogenetic control by post-translational phosphorylation has generated important regulatory insights into this process, especially focusing on coordinated control by the cyclin-dependent kinase Cdc28. more...
Organism:
Candida albicans
Type:
Expression profiling by array
Platform:
GPL19574
10 Samples
Download data: TXT
Series
Accession:
GSE64383
ID:
200064383
9.

Histone deacetylation at coding sequences adjusts transcription kinetics during Candida albicans morphogenesis.

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Candida albicans
Type:
Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing
Platforms:
GPL15149 GPL15645
31 Samples
Download data: TXT
Series
Accession:
GSE38427
ID:
200038427
10.

Histone deacetylation at coding sequences adjusts transcription kinetics during Candida albicans morphogenesis [RNA-seq]

(Submitter supplied) Transcriptome analysis of wild type and set3-deficient Candida albicans cells in yeast and hyphal morphological phases
Organism:
Candida albicans
Type:
Expression profiling by high throughput sequencing
Platform:
GPL15645
12 Samples
Download data: TXT
Series
Accession:
GSE38426
ID:
200038426
11.

Histone deacetylation at coding sequences adjusts transcription kinetics during Candida albicans morphogenesis [ChIP-seq]

(Submitter supplied) The dataset contains ChIP-Seq data of the Set3 and Hos2 proteins in Candida albicans, assayed in two morphological phases (yeast and hypha). The Set3 and Hos2 proteins in the respective strains carry 9myc epitopes and ChIP was performed with an anti-myc antibody. Included samples are the following: 1 input and 1 ChIP sample of an untagged wild type strain as negative control assayed in the yeast phase, 1 input and 3 ChIP biological replicates of the Set3-9myc strain in the yeast phase, 1 input and 2 ChIP biological replicates of the Set3-9myc strain in the hypha phase, 1 input and 2 ChIP biological replicates of the Hos2-9myc strain in the yeast phase, 1 input and 2 ChIP biological replicates of the Hos2-9myc strain in the hypha phase, 1 input and 3 ChIP biological replicates of Set3-9myc in a set1delta/delta background in the yeast phase.
Organism:
Candida albicans
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL15149
19 Samples
Download data: TXT
Series
Accession:
GSE38425
ID:
200038425
12.

The impact of the SCFA crotonate on Candida albicans and macrophage transcriptomes

(Submitter supplied) The effects of the SCFA crotonate on fungal and host transcriptomes were addressed, following infection of mouse bone marrow-derived macrophages(BMDMs) with Candida albicans.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21493
12 Samples
Download data: CSV
Series
Accession:
GSE234554
ID:
200234554
13.

Soybean toxin (SBTX) impairs fungal growth by interfering with molecular transport, carbohydrate/amino acid metabolism and drug/stress responses

(Submitter supplied) Soybean toxin (SBTX) is an antifungal protein from soybeans with broad growth and filamentation inhibitory activity against many fungi, including human and plant pathogenic species such as Candida albicans, Candida parapsilosis, Aspergillus niger, Penicillium herquei, Cercospora sojina, and Cerospora kikuchii. Understanding the mechanism by which SBTX acts on fungi and yeasts may contribute towards the design of novel antifungal drugs and/or for the development of transgenic plants resistant to pathogens. more...
Organism:
Candida albicans
Type:
Expression profiling by array
Platform:
GPL17199
8 Samples
Download data: TXT
Series
Accession:
GSE47364
ID:
200047364
14.

Ncs2* mediates in vivo virulence of pathogenic yeast through sulphur modification of cytoplasmic transfer RNA

(Submitter supplied) Fungal pathogens threaten ecosystems and human health. Understanding the molecular basis of their virulence is key to develop new treatment strategies. Here, we characterize NCS2*, a point mutation identified in a clinical baker's yeast isolate. Ncs2 is essential for 2-thiolation of tRNA and the NCS2* mutation leads to increased thiolation at body temperature. NCS2* yeast exhibits enhanced fitness when grown at elevated temperatures or when exposed to oxidative stress, inhibition of nutrient signalling, and cell-wall stress. more...
Organism:
Candida albicans
Type:
Other
Platform:
GPL22403
12 Samples
Download data: TXT
Series
Accession:
GSE199422
ID:
200199422
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