<HashMap><database>GEO</database><scores/><additional><omics_type>Genomics</omics_type><species>Homo sapiens</species><gds_type>Non-coding RNA profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE288266</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Quantitative profiling of RNA modifications enriched in non-membrane bound cellular structures using APEX-RNA-MS</name><description>The dynamic behavior of RNA underlies fundamental biological processes. RNA function is controlled by post-transcriptional modifications that are spatiotemporally regulated, but characterizing the distribution of modified RNA transcripts with subcellular resolution is a major challenge. Here we present APEX-RNA-MS, which combines APEX2 proximity labeling with LC-MS quantification of modified ribonucleotides. We use APEX-RNA-MS to characterize RNA modifications proximal to RNA-binding proteins enriched in non-membrane bound cellular structures. We measure changes in protein-proximal RNA modification levels upon induction of DNA damage foci and stress granules, consistent with previous studies using antibody-based imaging and biochemical fractionation. Further, we show that tRNA-specific modifications are proximal to G3BP1 and use RNA sequencing and RNA FISH to demonstrate the accumulation of multiple tRNAs in stress granules. Taken together, our work provides a general approach for characterizing the subcellular distribution of RNA modifications and reveals new insights into the composition and function of cellular condensates.</description><dates><publication>2026/05/12</publication></dates><accession>GSE288266</accession><cross_references><GSM>GSM8762529</GSM><GSM>GSM8762530</GSM><GSM>GSM8762531</GSM><GSM>GSM8762532</GSM><GSM>GSM8762533</GSM><GSM>GSM8762534</GSM><GSM>GSM8762535</GSM><GSM>GSM8762536</GSM><GPL>24676</GPL><GSE>288266</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>