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SRX8326484: GSM4547236: Control-E-L35-A_FPKM; Vitis vinifera; RNA-Seq
1 ILLUMINA (HiSeq X Ten) run: 34.6M spots, 10.4G bases, 3.7Gb downloads

Submitted by: NCBI (GEO)
Study: Integrated omics analysis reveals the norisoprenoid responses in Vitis vinifera L. cv. Cabernet Sauvignon berries to abscisic acid and synthetic auxin
show Abstracthide Abstract
The abscisic acid (ABA) increase and auxin decline are both indicators of ripening initiation in grape berry, and norisoprenoid accumulation also start at around the onset of ripening. To investigate the transcriptional and posttranscriptional regulation of the ABA and synthetic auxin 1-naphthaleneacetic acid (NAA) on norisoprenoid production, we performed time series GC-MS and RNA-seq analyses on Cabernet Sauvignon grape berries from pre-veraison to ripening. Higher levels of free norisoprenoids were found in ABA-treated mature berries in two consecutive seasons, and both free and total norisoprenoids were significantly increased by NAA in one season. The expression pattern of known norisoprenoid-associated genes in all samples and the up-regulation of specific alternative splicing isoforms of VviDXS and VviCRTISO in NAA-treated berries were predicted to contribute to it. Combined weighted gene co-expression network analysis (WGCNA) and promoter motif prediction analysis suggested that GATA26 and GATA28 could be potential regulators of norisoprenoid accumulation. Finally, the network analysis uncovered the interaction between previously identified switch genes, hormone-related genes and norisoprenoid-associated genes. Overall design: Twelve grape berry sample groups were used for RNA sequencing in this study, consisting of ABA1000, NAA100 and the control at the E-L 34, E-L 35 E-L 36 and E-L 38 stages, respectively.
Sample: Control-E-L35-A_FPKM
SAMN14891997 • SRS6646172 • All experiments • All runs
Organism: Vitis vinifera
Library:
Instrument: HiSeq X Ten
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: Three biological replicates for each sample were performed. A sub-sample of 50 berries were randomly selected from each biological replicate for RNA extraction. Total RNA was extracted from the frozen deseeded berries (whole pericarp) using a SpectrumTM Plant Total RNA Kit (Sigma-Aldrich, CA, USA). RNA integrity and quality were assessed by analysis with the Aglient 2100 Bioanalyzer. RNA libraries were prepared for sequencing using standard Illumina protocols
Experiment attributes:
GEO Accession: GSM4547236
Links:
Runs: 1 run, 34.6M spots, 10.4G bases, 3.7Gb
Run# of Spots# of BasesSizePublished
SRR1177340734,563,37110.4G3.7Gb2020-05-13

ID:
10830503

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