{"doi":"10.7554/elife.87900","title":"The lncRNA Malat1 inhibits miR-15/16 to enhance cytotoxic T cell activation and memory cell formation","abstract":"Proper activation of cytotoxic T cells via the T cell receptor and the costimulatory receptor CD28 is essential for adaptive immunity against viruses, intracellular bacteria, and cancers. Through biochemical analysis of RNA:protein interactions, we uncovered a non-coding RNA circuit regulating activation and differentiation of cytotoxic T cells composed of the long non-coding RNA Malat1 (Metastasis Associated Lung Adenocarcinoma Transcript 1) and the microRNA family miR-15/16. miR-15/16 is a widely and highly expressed tumor suppressor miRNA family important for cell proliferation and survival. miR-15/16 play important roles in T cell responses to viral infection, including the regulation of antigen-specific T cell expansion and memory. Comparative Argonaute-2 high-throughput sequencing of crosslinking immunoprecipitation (AHC) combined with gene expression profiling in normal and miR-15/16-deficient mouse T cells revealed a large network of hundreds of direct miR-15/16 target mRNAs, many with functional relevance for T cell activation, survival and memory formation. Among these targets, Malat1 contained the largest absolute magnitude miR-15/16-dependent AHC peak. This binding site was among the strongest lncRNA:miRNA interactions detected in the T cell transcriptome. We used CRISPR targeting with homology directed repair to generate mice with a 5-nucleotide mutation in the miR-15/16-binding site in Malat1 . This mutation interrupted Malat1 :miR-15/16 interaction, and enhanced the repression of other miR-15/16 target genes, including CD28. Interrupting Malat1 interaction with miR-15/16 decreased cytotoxic T cell activation, including the expression of interleukin 2 (IL-2) and a broader CD28-responsive gene program. Accordingly, Malat1 mutation diminished memory cell persistence in mice following LCMV Armstrong and Listeria monocytogenes infection. This study marks a significant advance in the study of long non-coding RNAs in the immune system by ascribing cell-intrinsic, sequence-specific in vivo function to Malat1 . These findings have implications for T cell-mediated autoimmune diseases, antiviral and anti-tumor immunity, as well as lung adenocarcinoma and other malignancies where Malat1 is overexpressed.","journal":"eLife","year":2023,"id":333398,"datarank":0.8549878869279512,"base_score":3.1780538303479458,"endowment":3.1780538303479458,"self_citation_contribution":0.47670807455219194,"citation_network_contribution":0.37827981237575936,"self_endowment_contribution":0.47670807455219194,"citer_contribution":0.37827981237575936,"corpus_percentile":null,"corpus_rank":null,"citation_count":23,"citer_count":17,"citers_with_citation_signal":16,"citers_with_endowment":16,"datacite_reuse_total":0,"is_dataset":false,"is_dataset_confidence":0.9525,"is_data_producer":true,"deposit_databanks":{"GEO":["GSE216565","GSE216113","GSE44404","GSE102321"]},"is_oa":true,"file_count":0,"downloads":0,"has_version_chain":false,"published_date":"2023-01-01","fair_score":null,"fair_percentile":null,"algorithm_id":"datarank_citation_only_1hop_v6","ranking_scope":"data_only","authors":[{"id":34051,"name":"John D. Gagnon","orcid":"0000-0001-6208-5781","position":1,"is_corresponding":false},{"id":526652,"name":"Wandi S. Zhu","orcid":"0000-0002-6734-9915","position":2,"is_corresponding":false},{"id":261952,"name":"Priscila Muñoz-Sandoval","orcid":"0009-0005-7225-2615","position":3,"is_corresponding":false},{"id":1061180,"name":"Simon K Wong","orcid":null,"position":4,"is_corresponding":false},{"id":1061181,"name":"Dimitre S Simeonov","orcid":null,"position":5,"is_corresponding":false},{"id":240960,"name":"Zhongmei Li","orcid":"0000-0001-8616-9568","position":6,"is_corresponding":false},{"id":232882,"name":"Rachel DeBarge","orcid":"0000-0001-9223-1364","position":7,"is_corresponding":false},{"id":15988,"name":"Matthew H. Spitzer","orcid":"0000-0002-5291-3819","position":8,"is_corresponding":false},{"id":30775,"name":"Alexander Marson","orcid":"0000-0002-2734-5776","position":9,"is_corresponding":false},{"id":34067,"name":"K. Mark Ansel","orcid":"0000-0003-4840-9879","position":10,"is_corresponding":false},{"id":286754,"name":"Benjamin D Wheeler","orcid":"0000-0001-5310-7213","position":0,"is_corresponding":true}],"reference_count":83,"raw_metadata":null,"created_at":"2026-07-19T01:09:39.719497Z","pmid":"38127070","pmcid":null,"fwci":null,"citation_percentile":null,"influential_citations":0,"oa_status":null,"license":null,"views":0,"total_file_size_bytes":0,"version_count":0,"fair_f":null,"fair_a":null,"fair_i":null,"fair_r":null,"fair_zscore":null,"fair_rationale":null,"fair_model":null,"fair_agent_version":null,"fair_fulltext_source":null,"fair_has_llm":null,"fair_computed_at":null,"clinical_trials":[],"software_tools":[],"db_accessions":[],"linked_datasets":[],"topics":[]}