<HashMap><database>GEO</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE325nnn/GSE325806/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Schmidtea mediterranea</species><gds_type>Expression profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE325806</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>The stability of m6A-marked transcripts is linked to cell identity in planarians [MTC KD]</name><description>Using Nanopore dRNA-Seq, we generated a high-confidence atlas of ~72,200 m6A sites (minimal methylation rate of 15% in at least two replicates) across the planarian transcriptome. We identified planarian m6A sites to be installed in a DRAYW context and to be highly enriched near stop codons. Upon depletion of METTL14 – a core component of the methyltransferase complex – we observed a significant reduction of m6A levels by 73.2%, as well as significant gene expression changes in 1059 genes. Loss of m6A resulted in up- as well as downregulation of genes, but cell type markers were found to be specifically represented in both gene classes.</description><dates><publication>2026/08/18</publication></dates><accession>GSE325806</accession><cross_references><GSM>GSM9613716</GSM><GSM>GSM9613717</GSM><GSM>GSM9613718</GSM><GSM>GSM9613719</GSM><GSM>GSM9613712</GSM><GSM>GSM9613713</GSM><GSM>GSM9613714</GSM><GSM>GSM9613715</GSM><GSM>GSM9613720</GSM><GPL>36736</GPL><GSE>325806</GSE><taxon>Schmidtea mediterranea</taxon><PMID>[42770330]</PMID></cross_references></HashMap>