<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Casas E</submitter><funding>Government of Catalonia | Agència de Gestió d&amp;apos;Ajuts Universitaris i de Recerca</funding><funding>Fundacio Internacional Josep Carreras</funding><funding>Centres de Recerca de Catalunya</funding><funding>Ministerio de Economía y Competitividad</funding><funding>Ministerio de Economía y Competitividad (MEC)</funding><funding>'la Caixa' Foundation ('la Caixa')</funding><funding>&amp;apos;la Caixa&amp;apos; Foundation</funding><pagination>4104-4119</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12264111</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>44(14)</volume><pubmed_abstract>PIWI-interacting RNAs (piRNAs) are small noncoding RNAs that silence transposons in the animal germline. PiRNAs are produced from long single-stranded noncoding transcripts, from protein-coding transcripts, as well as from transposons. While some sites that produce piRNAs are in deeply conserved syntenic regions, in general, piRNAs and piRNA-producing loci turnover faster than other functional parts of the genome. To learn about the sequence changes that contribute to the fast evolution of piRNAs, we set out to analyze piRNA expression between genetically different mice. Here we report the sequencing and analysis of small RNAs from the mouse male germline of four classical inbred strains, one inbred wild-derived strain and one outbred strain. We find that genetic differences between indivi</pubmed_abstract><journal>The EMBO journal</journal><pubmed_title>Genetic polymorphisms lead to major, locus-specific, variation in piRNA production in mouse.</pubmed_title><pmcid>PMC12264111</pmcid><funding_grant_id>PID2019-105278RB-I00</funding_grant_id><funding_grant_id>PID2019-111676GB-I00</funding_grant_id><funding_grant_id>BFU2015-70581</funding_grant_id><funding_grant_id>LCF/BQ/DI22/11940007</funding_grant_id><pubmed_authors>Mitjavila-Ventura A</pubmed_authors><pubmed_authors>Cebria J</pubmed_authors><pubmed_authors>Vavouri T</pubmed_authors><pubmed_authors>Casas E</pubmed_authors><pubmed_authors>Sierra P</pubmed_authors><pubmed_authors>Jimenez-Chillaron JC</pubmed_authors><pubmed_authors>Forcales SV</pubmed_authors><pubmed_authors>Moreta-Moraleda C</pubmed_authors><pubmed_authors>Pospisilik JA</pubmed_authors><pubmed_authors>Panzeri I</pubmed_authors></additional><is_claimable>false</is_claimable><name>Genetic polymorphisms lead to major, locus-specific, variation in piRNA production in mouse.</name><description>PIWI-interacting RNAs (piRNAs) are small noncoding RNAs that silence transposons in the animal germline. PiRNAs are produced from long single-stranded noncoding transcripts, from protein-coding transcripts, as well as from transposons. While some sites that produce piRNAs are in deeply conserved syntenic regions, in general, piRNAs and piRNA-producing loci turnover faster than other functional parts of the genome. To learn about the sequence changes that contribute to the fast evolution of piRNAs, we set out to analyze piRNA expression between genetically different mice. Here we report the sequencing and analysis of small RNAs from the mouse male germline of four classical inbred strains, one inbred wild-derived strain and one outbred strain. We find that genetic differences between indivi</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Jul</publication><modification>2026-07-15T06:30:11.157Z</modification><creation>2026-06-30T03:22:35.582Z</creation></dates><accession>S-EPMC12264111</accession><cross_references><pubmed>40474006</pubmed><doi>10.1038/s44318-025-00475-4</doi></cross_references></HashMap>