<HashMap><database>biostudies-other</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Dr. Chris, Andrew Brosnan</submitter><funding>European Molecular Biology Organization (EMBO)</funding><funding>EC | H2020 | H2020 Priority Excellent Science | H2020 European Research Council (ERC)</funding><journal>The EMBO Journal</journal><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-SCDT-EMBOJ-2018-100754</full_dataset_link><abstract>Loaded into ARGONAUTE(AGO) proteins, eukaryotic micro(mi)RNAs regulate gene expression via cleavage, translational repression and/or accelerated decay of sequence-complementary target transcripts. Despite their importance in development, cell identity-maintenance and stress responses, how individual miRNAs contribute to spatial gene regulation within the complex cell mosaics formed in tissues/organs has remained inaccessible in any organism to date. We have developed a non-invasive methodology to examine, at single-cell-type resolution, the AGO-loading and activity patterns of entire miRNA cohorts in intact organs, applied here to the Arabidopsis root-tip. A dual miRNAome-targetome analytical interface allowing intuitive data integration/visualization was developed as the basis for in-dept</abstract><repository>biostudies-other</repository><funding_grant_id>ALTF 728-2009</funding_grant_id><funding_grant_id>323071</funding_grant_id><pubmed_authors>Dr. Chris, Andrew Brosnan</pubmed_authors><pubmed_authors>Nicolas, Gerardo Bologna</pubmed_authors><pubmed_authors>Alexis Sarazin</pubmed_authors><pubmed_authors>Prof. Olivier Voinnet</pubmed_authors><pubmed_authors>Peiqi Lim</pubmed_authors><pubmed_authors>Matthias Hirsch-Hoffmann</pubmed_authors></additional><is_claimable>false</is_claimable><name>Genome-scale, single cell-type resolution of microRNA activities within a whole plant organ</name><description>Loaded into ARGONAUTE(AGO) proteins, eukaryotic micro(mi)RNAs regulate gene expression via cleavage, translational repression and/or accelerated decay of sequence-complementary target transcripts. Despite their importance in development, cell identity-maintenance and stress responses, how individual miRNAs contribute to spatial gene regulation within the complex cell mosaics formed in tissues/organs has remained inaccessible in any organism to date. We have developed a non-invasive methodology to examine, at single-cell-type resolution, the AGO-loading and activity patterns of entire miRNA cohorts in intact organs, applied here to the Arabidopsis root-tip. A dual miRNAome-targetome analytical interface allowing intuitive data integration/visualization was developed as the basis for in-dept</description><dates><release>2020-04-01T00:00:00Z</release><modification>2020-04-01T12:31:25Z</modification><creation>2020-04-01T12:31:25Z</creation></dates><accession>S-SCDT-EMBOJ-2018-100754</accession><cross_references><doi>10.15252/embj.2018100754</doi></cross_references></HashMap>