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Links from GEO DataSets

Items: 7

1.

Yeast glucosamine treatment

(Submitter supplied) We did transcription profiling on the effect of glucosamine in Saccharomyces cerevisiae using Research Genetics strains BY4741 (wild type) and 5251 (fks1). Yeast cells exposed to glucosamine in YPD growth medium show a significant increase in chitin content in the lateral cell wall. Likewise, cell wall stress caused by a gene deletion e.g., fks1 also results in elevated chitin. By comparing our data for fks1 with those from the literature we confirmed a strong induction of genes responsive to cell wall integrity, environmental stress as well as genes involved in cell signaling. more...
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by array
Dataset:
GDS344
Platform:
GPL90
11 Samples
Download data
Series
Accession:
GSE441
ID:
200000441
2.
Full record GDS344

Chitin synthesis

Investigation into chitin synthesis in wildtype BY4741 and mutant fks1 (elevated chitin). Cells exposed to chitin-inducing glucosamine either for 2 hours, or continuous steady state.
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by array, count, 3 protocol, 2 strain sets
Platform:
GPL90
Series:
GSE441
11 Samples
Download data
3.

Transcriptional response on ccw12 mutant from S. cerevisiae

(Submitter supplied) Ccw12p is a cell surface mannoprotein required for cell wall stability. To investigate the compensation mechanism after CCW12 deletion we analysed the global gene expression in ccw12 mutant cells.
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by array
Platform:
GPL90
4 Samples
Download data: CEL
Series
Accession:
GSE22649
ID:
200022649
4.

Global mRNA expression analysis in myo1 delta strains of the budding yeast Saccharomyces cerevisiae

(Submitter supplied) The Saccharomyces cerevisiae MYO1 gene encodes the myosin type II heavy chain (Myo1p), a protein required for normal cytokinesis in budding yeast. Deletion of the MYO1 gene prevents actomyosin-driven cytokinesis thereby activating an alternative mechanism that involves the synthesis of a remedial septum. Myo1p deficiency in yeast (myo1) also causes the formation of attached cells, abnormal budding patterns, formation of enlarged and elongated cells, increased osmotic sensitivity, delocalized chitin deposition, and increased chitin synthesis. more...
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by array
Platform:
GPL884
6 Samples
Download data: TXT
Series
Accession:
GSE5931
ID:
200005931
5.

Candida albicans DOPA-grown cells

(Submitter supplied) The fungal pathogen Candida albicans produces dark-pigmented melanin when grown in a basal medium containing 1 mM l-DOPA as melanin substrate. In the widely used C. albicans strain SC5314, melanin appeared after 3-4 days of incubation in l-DOPA medium. The experiment was designed to reveal cadidate genes associated with melanin biosynthesis by expression profiling at different times of growth with and without L-DOPA added to the medium. more...
Organism:
Candida albicans
Type:
Expression profiling by array
Platform:
GPL7476
16 Samples
Download data: TXT
Series
Accession:
GSE20338
ID:
200020338
6.

Signature gene expression profiles for cytokinesis mutants in the budding yeast Saccharomyces cerevisiae

(Submitter supplied) During cytokinesis in the budding yeast Saccharomyces cerevisiae, contraction of the cytokinetic ring and primary septum synthesis by chitin synthase II (Chs2p) are coupled processes. Myosin II (Myo1p), is involved in the actomyosin ring formation, required for proper cytokinesis, while Chs2p is responsible for the chitin primary septum formation which is necessary to stabilize the cytokinetic ring during its contraction. more...
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by array
Platform:
GPL2883
5 Samples
Download data: TXT
Series
Accession:
GSE12994
ID:
200012994
7.

Deletion of the Aspergillus niger pro-protein processing protease gene kexB results in a pH-dependent morphological transition during submerged cultivations and increases cell wall chitin content

(Submitter supplied) There is a growing interest for the use of post-fermentation mycelial waste to obtain cell wall chitin as an added-value product. In the pursuit to identify suitable production strains that can be used for post-fermentation cell wall harvesting, we turned to an Aspergillus niger strain in which the kexB (also named pclA in literature) gene was deleted. Previous work has shown that deletion of kexB causes hyper-branching and thicker cell walls, which is beneficial as these properties reduce fermentation viscosity and lysis. more...
Organism:
Aspergillus niger
Type:
Expression profiling by high throughput sequencing
Platform:
GPL25519
4 Samples
Download data: TSV
Series
Accession:
GSE151618
ID:
200151618
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