<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/GSE333nnn/GSE333657/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Homo sapiens</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=GSE333657</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Effect of PSNEAT1 knockout on gene expression and ribosome biogenesis in NCI-H1299 cells</name><description>Ribosomal DNA transcription is the initial and rate-limiting step of ribosome biogenesis and is tightly associated with nucleolar organization and tumor cell growth. PSNEAT1 is a nucleolar microprotein encoded by the NEAT1_1 transcript and has been shown to regulate rDNA transcription and nucleolar function. To investigate the transcriptional consequences of PSNEAT1 depletion, we generated PSNEAT1 knockout NCI-H1299 cells and performed RNA-seq analysis compared with control cells. Loss of PSNEAT1 resulted in broad gene expression changes associated with ribosome biogenesis, rRNA processing, nucleolar function, and cell growth-related pathways. These data provide a transcriptomic framework for understanding how PSNEAT1 contributes to nucleolar homeostasis and supports rDNA transcription-dependent tumor cell proliferation.</description><dates><publication>2026/09/07</publication></dates><accession>GSE333657</accession><cross_references><GSM>GSM9770547</GSM><GSM>GSM9770548</GSM><GSM>GSM9770549</GSM><GSM>GSM9770550</GSM><GSM>GSM9770551</GSM><GSM>GSM9770552</GSM><GPL>24676</GPL><GSE>333657</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>