<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/GSE328nnn/GSE328211/</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=GSE328211</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>eIF3 interactions with miRNAs involved in translational control of early T cell activation</name><description>Early T cell activation induces extensive remodeling of the cellular transcriptome and proteome. We previously showed using a transcriptome-wide crosslinking approach that human translation initiation factor eIF3 directly interacts with a select set of immune-related mRNAs shortly after T cell activation. We also found that eIF3 binding to the 3’-untranslated regions (3’-UTRs) of the TCRA and TCRB mRNAs encoding the T cell receptor alpha and beta subunits dynamically regulates a burst in their translation. MicroRNAs (miRNAs) add an additional layer of regulation by fine-tuning both mRNA and protein expression. Although miRNA expression is dynamically regulated during T cell activation, how miRNAs interact with core regulatory pathways in primary T cells remains poorly understood. Here, we reexamined the eIF3-RNA crosslinking experiments in Jurkat cells and probed eIF3 function to investigate miRNA-mediated translational regulation during T cell activation. We found that human eIF3 interacts with multiple mature miRNAs in activated Jurkat cells, including members of the miR-17-92 cluster. These interactions also occur in primary T cells, as shown by RNA immunoprecipitation followed by qPCR (RIP-qPCR). Knocking out the miR-17-92 cluster led to a delay in ILR2A (CD25) cell surface expression in Jurkat cells and reduced activation-associated cell size increase in primary T cells during early T cell activation. In parallel, we used mass spectrometry analysis of activated primary T cells to identify eIF3-interacting factors, and surprisingly found no evidence of Argonaute binding. Together, these findings provide evidence that eIF3-miRNA interactions may play an unappreciated role in translational control during early T cell activation.</description><dates><publication>2026/06/10</publication></dates><accession>GSE328211</accession><cross_references><GSM>GSM9675063</GSM><GSM>GSM9675052</GSM><GSM>GSM9675062</GSM><GSM>GSM9675051</GSM><GSM>GSM9675065</GSM><GSM>GSM9675054</GSM><GSM>GSM9675064</GSM><GSM>GSM9675053</GSM><GSM>GSM9675056</GSM><GSM>GSM9675055</GSM><GSM>GSM9675058</GSM><GSM>GSM9675057</GSM><GSM>GSM9675049</GSM><GSM>GSM9675059</GSM><GSM>GSM9675048</GSM><GSM>GSM9675061</GSM><GSM>GSM9675050</GSM><GSM>GSM9675060</GSM><GPL>24676</GPL><GSE>328211</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>