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SRX21538640: GSM7746516: SHS222Solar14DAFHeatSiliqueS20191; Brassica napus; RNA-Seq
1 ILLUMINA (Illumina NovaSeq 6000) run: 20.8M spots, 6.2G bases, 1.8Gb downloads

External Id: GSM7746516_r1
Submitted by: Plant Nutrition and Genomics Lab, Instituto de Bioquimica y Microbiologia, Universidad Austral de Chile
Study: Transcriptome and physiological analysis of rapeseed tolerance to post-flowering temperature increase
show Abstracthide Abstract
This study investigates the transcriptome and physiological responses of rapeseed to post-flowering temperature increases, providing valuable insights into the molecular mechanisms underlying rapeseed tolerance to heat stress. Two rapeseed genotypes, Lumen and Solar, were assessed under control and heat stress conditions in field experiments conducted in Valdivia, Chile. Results showed that seed yield and seed number were negatively affected by heat stress, with genotype-specific responses. Lumen exhibited a 9.3% average seed yield reduction, while Solar showed a 28.7% reduction. RNA-seq analysis of siliques and seeds revealed tissue-specific responses to heat stress, with siliques being more sensitive to temperature stress. Hierarchical clustering analysis identified distinct gene clusters reflecting different aspects of heat stress adaptation in siliques, with a role for protein folding in maintaining silique development and seed quality under high temperature conditions. In seeds, three distinct patterns of heat-responsive gene expression were observed, with genes involved in protein folding and response to heat showing genotype-specific expression. Gene coexpression network analysis revealed major modules for rapeseed yield and quality, as well as the trade-off between seed number and seed weight. Overall, this study contributes to understanding the molecular mechanisms underlying rapeseed tolerance to heat stress and can inform crop improvement strategies targeting yield optimization under changing environmental conditions. Overall design: Seed samples for the RNA-seq were collected from 5 plants per plot (25 siliques per plant from the bottom of the main raceme) across treatments in two development stages: 7 and 14 after flowering, i.e. after a one and twice weeks after the beginning of the heat stress treatment.
Sample: SHS222Solar14DAFHeatSiliqueS20191
SAMN37201491 • SRS18748064 • All experiments • All runs
Organism: Brassica napus
Library:
Name: GSM7746516
Instrument: Illumina NovaSeq 6000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: Total RNA extraction was performed using a method adapted for Brassica seeds (Graeber et al., 2011;doi:10.1105/tpc.111.084103) with 100 mg of each sample and using NucleoSpin® Gel and PCR columns RNA quality analysis, libraries construction and sequencing were performed by Novogene (Beijing, China) using standard Illumina protocols
Runs: 1 run, 20.8M spots, 6.2G bases, 1.8Gb
Run# of Spots# of BasesSizePublished
SRR2581645420,775,4206.2G1.8Gb2023-09-02

ID:
29022282

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