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SRX24523253: GSM8262593: H18; Pistacia vera; RNA-Seq
1 ILLUMINA (HiSeq X Ten) run: 8.5M spots, 2.6G bases, 939.2Mb downloads

External Id: GSM8262593_r1
Submitted by: Blanco Lab, Plant Sciences, University of California, Davis
Study: In a nutshell: pistachio genome and kernel development
show Abstracthide Abstract
Pistachio is a sustainable nut crop with exceptional climate resilience and nutritional value. To advance pistachios as a future food source and establish a model system for hard-shelled fruits, we generated essential knowledge and resources for the scientific community. We include a new chromosome-scale reference genome assembly and annotation of the most widely grown pistachio cultivar (Pistacia vera 'Kerman') and a spatiotemporal developmental study of the hull, shell, and kernel. Our study defined four distinct stages of pistachio growth and maturation by integrating tissue-level physiological and molecular data from thousands of nuts across twenty-four time points over three growing seasons. Transcriptional and metabolic changes in the kernel elucidate nutritional quality, such as the accumulation of unsaturated fatty acids, vital for shelf life and dietary value. This work yields new knowledge that will inform other woody crops and facilitate further improvement of pistachio as a globally significant, sustainable, and nutritious crop. Overall design: Gene expression analysis was performed on three pistachio tissues, hull (fruit exocarp), shell (fruit endocarp), and kernel (seed), across 15 weeks of fruit and seed development.
Sample: H18
SAMN41342287 • SRS21270903 • All experiments • All runs
Organism: Pistacia vera
Library:
Name: GSM8262593
Instrument: HiSeq X Ten
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: At each time point pistachio fruit hull (exocarp) and shell (endocarp), and kernel (seed) tissue were separated, and flash frozen with liquid nitrogen. Frozen tissue was lysed using a Retsch® Mixer Mill MM 400. A total of 1 gram of ground material was used during for RNA extraction as described in Blanco-Ulate et al., 2013. Purity and concentration of the extracted RNA were determined with the use of the NanoDrop One Spectrophotometer (Thermo Scientific), followed by a more precise concentration measurement with the Qubit 3 (Invitrogen). The integrity of the RNA was confirmed via agarose gel electrophoresis. cDNA libraries were prepared using the Illumina TruSeq RNA Sample Preparation Kit v.2 (Illumina, CA) from isolated RNA. Each library was barcoded and analyzed with the High Sensitivity DNA Analysis Kit for the Agilent 2100 Bioanalyzer (Agilent Technologies, CA). Libraries were sequenced as paired-end 150-bp reads on an Illumina Hiseq X Ten platform by IDseq
Runs: 1 run, 8.5M spots, 2.6G bases, 939.2Mb
Run# of Spots# of BasesSizePublished
SRR289961678,497,8252.6G939.2Mb2024-07-01

ID:
32840018

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