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SRX17699063: GSM6599909: P2_t24 rep3; Prunus persica; miRNA-Seq
1 ILLUMINA (Illumina HiSeq 2500) run: 1.3M spots, 63M bases, 27.5Mb downloads

External Id: GSM6599909_r1
Submitted by: Institute for Agricultural and Food Technology, Universitat de Girona
Study: miRNAs have a role on Prunus persica response to topic application of PpPep2 endogenous peptide
show Abstracthide Abstract
We charactarize the regulated miRNAs of Prunus persica to preventive treatment of PpPep2 1 µM endogenous peptide. The peptide treatment was applied to leaves and we sequenced the miRNAs after 1 and 24 h using untreated plants as control. miRNA profiles were generated by deep sequencing, in triplicate, using Illumina HiSeq 2500. Differential expression analysis of annotated pre_miRNA gene biotypes was performed with R package DESeq2 v1.26.0, considering significant epression values below FDR <0.05. We obtained 117,267,647 raw reads and we identified a total of 33 differential expressed miRNAs (DEM) belonging to 18 miRNA families upon PpPep2 application, accounting for 15% of the P. persica annotated miRNAs. miRNA regulation occurs principally one day after peptide treatment. The predicted mRNA targets and function of orthologous miRNAs are compatible with a regulation of PTI-related processes. Together with the transcriptomic response of P. persica to PpPep2 described at our previous RNA-Seq (Foix et al 2021), this suggests that miRNAs would have an active role in PTI regulation at these stages. Overall design: miRNA profiles of P. persica pretreated with PpPep2 after 1 and 24 h (t1, t24 h), untreated plants as control (t0).
Sample: P2_t24 rep3
SAMN31010897 • SRS15229799 • All experiments • All runs
Organism: Prunus persica
Library:
Name: GSM6599909
Instrument: Illumina HiSeq 2500
Strategy: miRNA-Seq
Source: TRANSCRIPTOMIC
Selection: size fractionation
Layout: SINGLE
Construction protocol: RNA was extracted from a 200 mg aliquot of ground leaf sample through a TRIzol-based procedure (Invitrogen Life Technologies, Carlsbad, CA, USA) followed by DNAse I (Ambion, Grand Island, NY, USA) digestion and purification with RNeasy MinElute Cleanup Kit (Qiagen, Sollentuna, Sweden). Estimation of RNA concentration was using a NanoDrop ND1000 spectrophotometer (Nanodrop Technologies, Wilmington, DE, USA). miRNA-Seq was carried out at the National Centre for Genomics Analysis (Barcelona, Spain). Libraries were prepared using the NEBNext® Small RNA Library Prep Set for Illumina® kit (ref. E7330) according to the manufacturer's protocol. Briefly, RNA was subjected to adaptor 3´and 5´ ligation and first strand cDNA synthesis. Then, DNA fragments having adapter molecules on both ends were selectively enriched by PCR. Library amplification was performed by using NEBNext® Multiplex Oligos for Illumina (Index Primers Set 1, ref. E7335, Index Primers Set 2, ref. E7500, Index Primers Set 3, ref. E7710 and Index Primers Set 4, ref. E7730). Purification steps were then performed using AgenCourt AMPure XP beads (ref. A63882, Beckman Coulter) and final libraries were analyzed using Agilent Bioanalyzer (ref. 5067-4626) to estimate the quantity and check size distribution. A pool was done to perform size selection using 6% Novex TBE PAGE Gels (ref. EC6265BOX) and then the final pool was quantified by qPCR using the KAPA Library Quantification Kit (ref. KK4835, KapaBiosystems) prior to amplification with Illumina's cBot. Libraries were sequenced 1 * 50+8 bp on Illumina HiSeq2500 device
Runs: 1 run, 1.3M spots, 63M bases, 27.5Mb
Run# of Spots# of BasesSizePublished
SRR217015331,260,34863M27.5Mb2024-12-19

ID:
24601245

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