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Series GSE158756 Query DataSets for GSE158756
Status Public on Sep 30, 2020
Title Transcriptome analysis of programmed cell death during allorecognition in Cryphonectria parasitica
Organism Cryphonectria parasitica
Experiment type Expression profiling by high throughput sequencing
Summary The underlying molecular mechanisms of programmed cell death (PCD) associated with fungal allorecognition, a form of innate immunity, remain largely unknown. In this study, transcriptome analysis was used to infer mechanisms activated during barrage formation in vic3-incompatible strains of C. parasitica, the chestnut blight fungus. Pronounced differential expression occurred in barraging strains of genes involved in mating pheromone (mf2-1, mf2-2), secondary metabolite production, detoxification (including oxidative stress), apoptosis-related, RNA interference and HET-domain genes. Evidence for secondary metabolite production and reactive oxygen species (ROS) accumulation is supported through UPLC-HRMS analysis and cytological staining, respectively. Differential expression of mating-related genes and HET-domain genes was further examined by RT-qPCR of incompatible interactions involving each of the 6 vegetative incompatibility (vic) loci in C. parasitica and revealed distinct recognition process networks. We infer that vegetative incompatibility in C. parasitica activates defence reactions that involve secondary metabolism, resulting in increased toxicity of the extra- and intracellular environment. Accumulation of ROS (and other potential toxins) may result in detoxification failure and activation of apoptosis, sporulation, and the expression of associated pheromone genes. The incompatible reaction leaves abundant traces of a process-specific metabolome as conidiation is initiated.
 
Overall design Identification of genes involved in allorecognition in C. parasitica. Total 15 samples: 5 samples with 3 replicas. Controls: 3 monoculture strains (P74-3, EP155, DZ-66), 1 mix strain sample (P74-3+DZ-66). Experiment: 1 mix strain sample (P74-3+P155).
 
Contributor(s) Belov AA, Witte T, Overy DP, Smith ML
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Submission date Sep 29, 2020
Last update date Oct 01, 2020
Contact name Myron Smith
E-mail(s) myronsmith@cunet.carleton.ca
Organization name Carleton University
Department Biology
Street address 1125 Colonel By drive
City Ottawa
State/province Ontario
ZIP/Postal code K1S 5B6
Country Canada
 
Platforms (1)
GPL29197 Illumina NovaSeq 6000 (Cryphonectria parasitica)
Samples (15)
GSM4809854 E2 - EP155
GSM4809855 E3 - EP155
GSM4809856 E4 - EP155
Relations
BioProject PRJNA666425
SRA SRP285806

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE158756_count_matrix.csv.gz 386.8 Kb (ftp)(http) CSV
GSE158756_nov_seqs.fasta.gz 431.7 Kb (ftp)(http) FASTA
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

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