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SRX4300137: GSM3223386: Si rep2; Cucumis sativus; RNA-Seq
1 ILLUMINA (Illumina HiSeq 2500) run: 11.7M spots, 2.9G bases, 1,016.9Mb downloads

Submitted by: NCBI (GEO)
Study: Transcriptomic dynamics provides an insight into the mechanism for silicon-mediated alleviation of salt stress in cucumber plants
show Abstracthide Abstract
Salinity seriously reduces the yield and quality of crops. Silicon (Si) has been widely reported to have beneficial effects on plant growth and development under salt stress. However, the mechanism is still poorly understood. In an attempt to identify genes or gene networks that may be orchestrated to improve salt tolerance of cucumber plants, we profiled the RNA-seq transcriptomes of both control and salt-stressed cucumber leaves in the presence or absence of added Si. The comparative transcriptome analysis revealed that Si plays an important role in shaping the transcriptome of cucumber: the expression levels of >1,000 genes (differtially expressed genes, DEGs) were changed in response to Si treatment as compared with the control, and these genes were mainly involved in ion transport, hormone and signal transduction, biosynthesis and metabolic processes, stress and defense responses, and antioxidant activity. Under salt stress, many genes functionally associated with metabolic processes and responses to environmental stimuli were strongly up- or down-regulated in their expressions. Si treatment showed a tendency that induced the transcriptomic profile of salt-stressed cucumber back to that of the control with large majority of Na down-regulated DEGs and about half of Na up-regulated DEGs being adjusted back to CT levels. This study provides a novel insight into the mechanism for Si-mediated alleviation of salt stress in plants at the transcriptome level, and it suggests that Si may act as an elicitor to precondition cucumber plants and induce salt tolerance. Overall design: Transcriptome profiles of both control and salt-stressed cucumber leaves in the presence or absence of added Si were generated by deep sequencing, in triplicates, using Illumina HiSeq 2500.
Sample: Si rep2
SAMN09487597 • SRS3462955 • All experiments • All runs
Organism: Cucumis sativus
Library:
Instrument: Illumina HiSeq 2500
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: Total RNA was harvested using Trizol reagent following manufacture`s protocol (Roche, Mannheim, Germany). RNA-Seq library construction and sequencing were conducted by Gene Denovo Co. (Guangzhou, China). The poly(A)-containing mRNA molecules were purified from 10 mg of total RNA using poly-T oligo-attached magnetic beads. The extracted mRNAs were fragmented into 200-bp-long pieces using RNA Fragmentation Buffer (Kapa, Biosystems). The cleaved Illumina Sequencing mRNA fragments were reverse-transcripted into first-strand cDNA using random primers, followed by second-strand cDNA synthesis using DNA Polymerase I and RNase H. Then, the cDNA fragments went through an end repair process, the addition of a single “A” base, and ligation of the adapter sequences. Finally, the cDNA products were purified and enriched to construct libraries for non-strand-specific RNA-Seq.
Experiment attributes:
GEO Accession: GSM3223386
Links:
Runs: 1 run, 11.7M spots, 2.9G bases, 1,016.9Mb
Run# of Spots# of BasesSizePublished
SRR742931511,718,7442.9G1,016.9Mb2020-04-17

ID:
5787522

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