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Sample GSM6893731 Query DataSets for GSM6893731
Status Public on Dec 12, 2023
Title SI_4h3
Sample type SRA
 
Source name Fludioxonil treat
Organism Botrytis cinerea
Characteristics strain: BC-57
tissue: mycelia
Treatment protocol S (fludioxonil-sensitive), FR (fludioxonil resistance from field), and LR (fludioxonil resistance from laboratory) were routinely cultivated on PDA for three days. For each fungal strain, eight mycelium plugs (5 mm) were incubated using a 200 mL potato dextrose broth (PDB) medium for two days at 23°C and shaken at 180 rpm. The resulting mycelia were treated with or without fludioxonil. In detail, the 10 mg/L fludioxonil stock solutions were added to the PDB medium at final concentrations of 0.05 μg/mL for S, 10 μg/mL for FR, and 500 μg/mL for LR, and the same volume of acetone was added to the 200 mL PDB medium to prepare the control samples. The fludioxonil-induced and no-induced (control) samples were cultured under the same conditions (at 23°C and 180 rpm) for 4 h before RNA extraction. Six samples in total were collected for the following RNA manipulations, i.e., fludioxonil-induced and no-induced S (designated as SI_4h and S_4h), fludioxonil-induced and no-induced LR (designated as LRI_4h and LR_4h), and fludioxonil-induced and no-induced FR (designated as FRI_4h and FR_4h, respec-tively).
Growth protocol The B. cinerea strains, BC-2 and BC-57, used in this study, were isolated from typical gray mold symptom tomato leaves found in local greenhouses (Beijing City). Both of the B. cinerea isolates were first purified using single spore isolation and thereafter main-tained on potato dextrose agar (PDA, 200 g/L potato, 20 g/L agar, and 20 g/L dextrose). After approximately three days of dark-incubation at 23°C, B. cinerea mycelia were ob-tained from the edge of the colonies and transferred to the PDA slants and preserved at 15°C in darkness.
Extracted molecule total RNA
Extraction protocol Mycelium of the parent fludioxonil-sensitive strain (S), laboratory fludioxo-nil-resistant strain (LR), and field fludioxonil-resistant strains were obtained as de-scribed above. All of the isolates were grown at the same time for the same amount of time (three days) under the same conditions (shaking at 23°C and 180 rpm) in PDB. The mycelium were then collected at the same time. RNA was extracted from samples using the TRIzol method (Invitro Corp., Carlsbad, CA, USA).The RNA concentration and quality were assessed using a nanodrop and gelelectrophoresis. The samples were stored at ?80°C.
RNA sequencing was conducted by Novogene using an Illumina? (San Diego, CA, USA) based method to generate 20 million 150-bp paired-end reads per sample. The se-quencing library was prepared with the NEBNext? Ultra?RNA Library Prep Kit for Illumina?, and sequencing was performed on the NovaSeq PE150.
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina NovaSeq 6000
 
Data processing Raw reads stored in the fastq format after the Illumina sequencing were first pro-cessed through in-house perl scripts. In this step, clean reads were obtained by re-moving reads containing adapter, reads containing ploy-N, and low quality reads from the raw data. Clean reads were generated with high quality that were assessed by pa-rameters of the Q20, Q30, and GC contents.
Assembly: Botrytis cinerea B05.10 reference genome (GenBank accession number: GCA_000143535.4)
Supplementary files format and content: tab-delimited text files include FPKM values for each Sample.
 
Submission date Dec 24, 2022
Last update date Dec 12, 2023
Contact name Xuncheng Wang
E-mail(s) 1706380435@pku.edu.cn
Organization name Peiking University
Street address 5 Yiheyuan Road
City Beijing
ZIP/Postal code 100871
Country China
 
Platform ID GPL32786
Series (1)
GSE221721 Transcriptomic analysis of resistant and wild-type Botrytis ci-nerea isolates revealed fludioxonil-resistant mechanisms
Relations
BioSample SAMN32398583
SRA SRX18847354

Supplementary file Size Download File type/resource
GSM6893731_SI_4h3.FPKM.txt.gz 97.0 Kb (ftp)(http) TXT
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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