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Links from GEO DataSets

Items: 20

1.

Deciphering regulatory mechanisms associated with hemicellulose degradation in Neurospora crassa

(Submitter supplied) Hemicellulose, the second most abundant plant biomass fraction after cellulose, is widely viewed as a potential feedstock for the production of liquid fuels and other value-added materials. Degradation of hemicellulose by filamentous fungi requires production of many different enzymes, which are induced by biopolymers or its derivatives and regulated mainly at the transcriptional level through transcription factors (TFs). more...
Organism:
Neurospora crassa
Type:
Expression profiling by array
Platform:
GPL14949
23 Samples
Download data: GPR, TXT
Series
Accession:
GSE34098
ID:
200034098
2.

Conserved and Essential Transcription Factors for Cellulase Gene Expression in Ascomycete Fungi.

(Submitter supplied) Transcriptional profiling with next-generation sequencing methods refined our understanding of the N. crassa transcriptional response to cellulose and demonstrated that the newly characterized transcription factors clr-1 and clr-2 were required for the bulk of that response including induction all major cellulase and some major hemicellulase genes.
Organism:
Neurospora crassa OR74A
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL15146 GPL15147
26 Samples
Download data: TXT
Series
Accession:
GSE35227
ID:
200035227
3.

Transcriptional profiling of the Neurospora crassa Δcre-1 mutant (FGSC 10372) compared to the wild type strain (FGSC 2489) in response to minimal medium or Avicel medium

(Submitter supplied) In filamentous ascomycete fungi, the utilization of alternate carbon sources is influenced by the zinc finger transcription factor CreA/CRE-1, which encodes a carbon catabolite repressor protein homologous to Mig1 from Saccharomyces cerevisiae. In Neurospora crassa, deletion of cre-1 results in increased secretion of amylase and β-galactosidase. Here, we determined the CRE-1 regulon by investigating the transcriptome of a Δcre-1 strain compared to wild type when grown on Avicel versus minimal medium (MM). more...
Organism:
Neurospora crassa
Type:
Expression profiling by array
Platform:
GPL13956
8 Samples
Download data: GPR, TXT
Series
Accession:
GSE30313
ID:
200030313
4.

VIB1, a link between glucose signaling and carbon catabolite repression, is essential for plant cell wall degradation by Neurospora crassa

(Submitter supplied) Purpose: To explore the function of VIB1 in regulating cellulase production in Neurospora crassa. Method: mRNA from vib-1 mutants were collected after a culture shift from sucrose to Avicel (crystaline cellulose) or carbon-free media. Expression profiles of vib-1 mutants were compared with published profiles of wild type created under the same conditions. Results: We found that many genes that specifically upregulated in wild type upon exposure to Avicel were expressed at low levels in ∆vib-1 and many other genes involved in metabolism and energy were expressed at high levels compared to wild type. more...
Organism:
Neurospora crassa
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL17918 GPL16164
9 Samples
Download data: FPKM_TRACKING
Series
Accession:
GSE52316
ID:
200052316
5.

The transcriptional factor Clr-5 is involved in cellulose degradation through regulation of amino acid metabolism in Neurospora crassa

(Submitter supplied) Filamentous fungi are one of the primary degraders of plant biomass because of their ability to produce enzymes that break down complex polysaccharides. The production of cellulolytic enzymes in fungi is dependent on transcription factors. In this article, we identified a N. crassa Zn2Cys6 transcription factor Clr5 that regulates the expression of cellulase on cellulose. N. crassa Δclr5 exhibited a significant decrease in secreted proteins (~46%), endo-glucanase (~55%), xylanase (~33%), β-glucosidase (~38%), and exocellulase (~40%) compared with the WT, while transcriptomic analysis revealed that clr5 was essential in cellulase expression. more...
Organism:
Neurospora crassa
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16164
12 Samples
Download data: XLSX
Series
Accession:
GSE222372
ID:
200222372
6.

Induction of lignocellulose-degrading enzymes in Neurospora crassa by cellodextrins

(Submitter supplied) Transcriptional profiling with next-generation sequencing methods demonstrated that a Neurospora crassa mutant with the three most highly expressed beta-glucosidase genes deleted had a transcriptional response to cellobiose similair to that of wild type N. crassa exposed to cellulose.
Organism:
Neurospora crassa OR74A
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL15147 GPL15146
13 Samples
Download data: TXT
Series
Accession:
GSE36719
ID:
200036719
7.

Identification of direct target genes of the Neurospora crassa essential plant biomass deconstruction transcription factors CLR-1, CLR-2 and XLR-1

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Neurospora crassa
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL16164
33 Samples
Download data: TXT
Series
Accession:
GSE68517
ID:
200068517
8.

Identification of direct target genes of the Neurospora crassa essential plant biomass deconstruction transcription factors CLR-1, CLR-2 and XLR-1 (ChIP-Seq)

(Submitter supplied) abstract: The plant cell wall is composed of many complex polymers, and its deconstruction requires an equally complex orchestration of a wide array of enzymes. In Neurospora crassa, clr-1, clr-2 and xlr-1 have been identified as the key transcription factors involved in cell wall breakdown. In order to define their regulons, we performed ChIPseq upon these three transcription factors. CLR-1, CLR-2 and XLR-1 each bind to the most highly and differentially expressed gene populations, which include the cellulases for the CLRs and the hemicellulases for XLR-1. more...
Organism:
Neurospora crassa
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL16164
22 Samples
Download data: XLSX
Series
Accession:
GSE68516
ID:
200068516
9.

Identification of direct target genes of the Neurospora crassa essential plant biomass deconstruction transcription factors CLR-1, CLR-2 and XLR-1 (RNA-Seq)

(Submitter supplied) abstract: The plant cell wall is composed of many complex polymers, and its deconstruction requires an equally complex orchestration of a wide array of enzymes. In Neurospora crassa, clr-1, clr-2 and xlr-1 have been identified as the key transcription factors involved in cell wall breakdown. In order to define their regulons, we performed ChIPseq upon these three transcription factors. CLR-1, CLR-2 and XLR-1 each bind to the most highly and differentially expressed gene populations, which include the cellulases for the CLRs and the hemicellulases for XLR-1. more...
Organism:
Neurospora crassa
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16164
11 Samples
Download data: TXT
Series
Accession:
GSE68514
ID:
200068514
10.

Inducer Free Cellulase Secretion in Neurospora Crassa and comparitive analysis of cellulase induction in Aspergillus nidulans

(Submitter supplied) Purpose: To explore conservation of gene regulation by the transcription factor clr-2/clrB in Neurospora crassa and Aspergillus nidulans Methods: mRNA from wild type and clr-2/clrB mutants were collected after a culture shift from sucrose/glucose to Avicel (crystaline cellulose) or no carbon media Results: We show that N. crassa and A. nidulans have similair global transcriptional responses to Avicel, with several hundred genes showing specific induction, though the induced genes are more specifically targeted at cellulose for N. more...
Organism:
Neurospora crassa OR74A; Aspergillus nidulans FGSC A4
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL15146 GPL16600 GPL15147
22 Samples
Download data: FPKM_TRACKING, TXT
Series
Accession:
GSE44100
ID:
200044100
11.

Expression analysis of Trichoderma reesei QM9414 and delta-blr1, delta-blr2 and delta-env1 in light and darkness

(Submitter supplied) Investigation of whole genome gene expression level changes in response to different light conditions of the T. reesei QM9414 deletion strains delta-blr1, delta-blr2 and delta env1 cultivated on 1% microcrystalline cellulose. Perception and proper interpretation of environmental signals is crucial for survival in any natural habitat. Although the biotechnological workhorse Trichoderma reesei (Hypocrea jecorina) is predominantly known for its capability of efficient plant cell wall degradation, recent studies show that it has not lost its evolutionary heritage. more...
Organism:
Trichoderma reesei
Type:
Expression profiling by array
Platform:
GPL10642
16 Samples
Download data: CALLS, PAIR
Series
Accession:
GSE36448
ID:
200036448
12.

The role of photoreceptors in the light modulated cellulase gene expression in Neurospora crassa

(Submitter supplied) Light represents an important environmental cue, which exerts considerable influence on the metabolism of fungi. Studies with the biotechnological fungal workhorse Trichoderma reesei (Hypocrea jecorina) have revealed an interconnection between transcriptional regulation of cellulolytic enyzmes and the light response. The filamentous fungus, Neurospora crassa, has been used as a model organism to study light and circadian rhythm biology. more...
Organism:
Neurospora crassa
Type:
Expression profiling by array
Platform:
GPL13956
20 Samples
Download data: GPR
Series
Accession:
GSE32871
ID:
200032871
13.

Deciphering the Regulatory Network between the SREBP pathway and Protein Secretion in Neurospora crassa

(Submitter supplied) Sterol Regulatory Element Binding Proteins (SREBPs) are conserved from yeast to mammalian cells and function in regulating sterol homeostasis. In fungi, the SREBP pathway has been implicated in the adaptation to hypoxia and in virulence. In Neurospora crassa and Trichoderma reesei, the SREBP pathway also negatively regulates protein secretion under lignocellulolytic conditions. Here we utilized global transcriptional profiling combined with genetic and physiological analyses to address the regulatory link between the SREBP pathway and protein secretion in N. more...
Organism:
Neurospora crassa
Type:
Expression profiling by high throughput sequencing
Platform:
GPL23150
12 Samples
Download data: FPKM_TRACKING
Series
Accession:
GSE95807
ID:
200095807
14.

Growth, enzymatic, and transcriptomic analysis of xyr1 deletion reveals a major regulator of plant biomass-degrading enzymes in Trichoderma harzianum

(Submitter supplied) The regulation of plant biomass degradation by fungi is critical to the carbon cycle, and applications in bioproducts and biocontrol. Trichoderma harzianum is an important plant biomass degrader, enzyme producer, and biocontrol agent, but few putative major transcriptional regulators have been deleted in this species. The T. harzianum ortholog of the transcriptional activator XYR1/XlnR/XLR-1 was deleted, and the mutant strains were analyzed by growth profiling, enzymatic activities, and transcriptomics on cellulose. more...
Organism:
Trichoderma harzianum
Type:
Expression profiling by high throughput sequencing
Platform:
GPL34038
18 Samples
Download data: TXT
Series
Accession:
GSE252008
ID:
200252008
15.

A comparative systems analysis of polysaccharide-elicited responses in Neurospora crassa reveals carbon source-specific cellular adaptations

(Submitter supplied) Filamentous fungi are powerful producers of hydrolytic enzymes for the deconstruction of plant cell wall polysaccharides. However, the central question of how these sugars are perceived in the context of the complex cell wall matrix remains largely elusive. To address this question in a systematic fashion we performed an extensive comparative systems analysis of how the model filamentous fungus Neurospora crassa responds to the three main cell wall polysaccharides: pectin, hemicellulose and cellulose. more...
Organism:
Neurospora crassa OR74A
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL15146 GPL15147
15 Samples
Download data: TXT
Series
Accession:
GSE42692
ID:
200042692
16.

Myceliophthora thermophila Xyr1 is predominantly involved in xylan degradation and xylose catabolism

(Submitter supplied) The aim of this study is to investigate the role of the transcription factor Xyr1 in the regulation of cellulolytic and xylanolytic genes of the filamantous fungus Myceliophthora thermophila
Organism:
Thermothelomyces thermophilus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL27455
20 Samples
Download data: XLS
Series
Accession:
GSE137286
ID:
200137286
17.

Transcriptional profiling of Neurospora crassa conidia undergoing germling fusion: Δpp-1 vs WT

(Submitter supplied) To study the consequences of transcription factor pp-1 deletion during vegetative cell fusion, we sequenced mRNA of WT and Δpp-1 conidia during a period of intense germling fusion activity .
Organism:
Neurospora crassa OR74A
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17654
2 Samples
Download data: TXT
Series
Accession:
GSE50446
ID:
200050446
18.

Transcriptional profiling of Neurospora crassa conidia undergoing a time-course: Δpp-1 vs WT

(Submitter supplied) To study the consequences of transcription factor pp-1 deletion during vegetative cell fusion, we performed whole genome microarrays of WT and Δpp-1 conidia during their initial growth period (3h - 8h).
Organism:
Neurospora crassa; Neurospora crassa OR74A
Type:
Expression profiling by array
Platform:
GPL13956
35 Samples
Download data: GPR, TXT
Series
Accession:
GSE49679
ID:
200049679
19.

Transcriptional profiling of Neurospora crassa cells containing MAK2Q100G allele: Exposure to ATP-analog (1NM-PP1) vs control

(Submitter supplied) To study the consequences of MAK-2 activity modulation during vegetative cell fusion, we took advantage of a previously constructed allele of MAK-2 (MAK-2Q100G) to specifically perturb kinase signaling during germling vegetative cell fusion (inhibition of MAK-2Q100G activity by addition of the ATP analog 1NM-PP1 results in a phenotype indistinguishable from mak-2 deletion strains). Whole genome microarrays of mak-2Q100G cells following 20 min 1NM-PP1 treatment were performed.
Organism:
Neurospora crassa; Neurospora crassa OR74A
Type:
Expression profiling by array
Platform:
GPL13956
7 Samples
Download data: GPR
Series
Accession:
GSE46912
ID:
200046912
20.

Aspects of the Neurospora crassa sulfur starvation response are revealed by transcriptional profiling and DNA affinity purification sequencing

(Submitter supplied) Accurate nutrient sensing is important for rapid fungal growth and exploitation of available resources. Sulfur is an important nutrient source found in a number of biological macromolecules, including proteins and lipids. The model filamentous fungus Neurospora crassa is capable of utilizing sulfur found in a variety of sources from amino acids to sulfate. During sulfur starvation, the transcription factor CYS-3 is responsible for upregulation of genes involved in sulfur uptake and assimilation. more...
Organism:
Neurospora crassa
Type:
Expression profiling by high throughput sequencing
Platform:
GPL30082
12 Samples
Download data: TXT, XLSX
Series
Accession:
GSE173890
ID:
200173890
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