<HashMap><database>ENA</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR217/039/SRR21701539/SRR21701539.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR217/035/SRR21701535/SRR21701535.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR217/041/SRR21701541/SRR21701541.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR217/034/SRR21701534/SRR21701534.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR217/037/SRR21701537/SRR21701537.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR217/033/SRR21701533/SRR21701533.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR217/040/SRR21701540/SRR21701540.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR217/036/SRR21701536/SRR21701536.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR217/038/SRR21701538/SRR21701538.fastq.gz</Fastqsanger.gz></files><type>primary</type></body><statusCodeValue>200</statusCodeValue><statusCode>OK</statusCode></file_versions><scores/><additional><omics_type>Genomics</omics_type><center_name>Institute for Agricultural and Food Technology, Universitat de Girona</center_name><full_dataset_link>https://www.ebi.ac.uk/ena/browser/view/PRJNA884105</full_dataset_link><scientific_name>Prunus persica</scientific_name><long_description>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 &lt;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).</long_description><tag>xref:PubMed:39684809</tag><repository>ENA</repository></additional><is_claimable>false</is_claimable><name>miRNAs have a role on Prunus persica response to topic application of PpPep2 endogenous peptide</name><description>miRNAs have a role on Prunus persica response to topic application of PpPep2 endogenous peptide</description><dates><last_updated>2025-09-24</last_updated><first_public>2024-12-21</first_public></dates><accession>PRJNA884105</accession><cross_references><GEO>GSE214135</GEO><taxon>3760</taxon><PubMed>39684809</PubMed></cross_references></HashMap>