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SRX18050979: GSM6690394: B05.10, LP, without nitrogen, rep 1; Botrytis cinerea; RNA-Seq
1 ILLUMINA (Illumina NovaSeq 6000) run: 30.5M spots, 9.2G bases, 2.7Gb downloads

External Id: GSM6690394_r1
Submitted by: Plant Nutrition and Genomics Lab, Instituto de Bioquimica y Microbiologia, Universidad Austral de Chile
Study: The clock protein FREQUENCY (BcFRQ1) in Botrytis cinerea is required for normal mitochondrial function and has an extra-circadian role in nitrogen metabolism
show Abstracthide Abstract
A functional circadian clock was previously characterized in Botrytis cinerea and demonstrated the crucial role of BcFRQ, the ortholog of core clock component FREQUENCY from Neurospora crassa. It was previously shown that the corresponding knockout mutant ?bcfrq displayed an abnormal developmental phenotype (always-sclerotia) when grown on potato dextrose agar. In the present study, we demonstrate that this phenotype can be reversed back to macroconidia production by adding primary nitrogen sources, suggesting an extra-circadian role for BcFRQ in nitrogen metabolism. We performed an RNAseq study of wildtype and knockout mutant ?bcfrq under varying nutritional and light conditions, to identify the genes involved in 1) perturbed nitrogen metabolism in the mutant ?bcfrq and 2) additional extra-circadian functions of BcFRQ. Overall design: Comparative gene expression profiling analysis of RNA-seq data for Botrytis cinerea strains (B05.10 and DeltaBcFRQ1) on CM media without nitrogen sources and complemented with Glutamine 0.1M as a primary source of Nitrogen. Samples were treated with constant light (LL), constant darkness (DD) or a light pulse (LP, 4 hours) and harvested at 48 hours.
Sample: B05.10, LP, without nitrogen, rep 1
SAMN31493675 • SRS15557291 • All experiments • All runs
Library:
Name: GSM6690394
Instrument: Illumina NovaSeq 6000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: RNA was harvested using Trizol and cleaned up with Qiagen RNAeasy Plant Minikit. 500 uL at 600ng/uL were send to Macrogen for the construction of sequencing libraries and sequencing. RNA libraries for RNA-seq were prepared by TruSeq stranded mRNA library in Macrogen.
Runs: 1 run, 30.5M spots, 9.2G bases, 2.7Gb
Run# of Spots# of BasesSizePublished
SRR2207061230,538,6509.2G2.7Gb2022-11-15

ID:
25013436

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