<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zhang Y</submitter><funding>National Natural Science Foundation of China</funding><funding>National Natural Science Foundation of China (National Science Foundation of China)</funding><pagination>126</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7987995</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>6(1)</volume><pubmed_abstract>The efficient induction and long-term persistence of pathogen-specific memory CD8 T cells are pivotal to rapidly curb the reinfection. Recent studies indicated that long-noncoding RNAs expression is highly cell- and stage-specific during T cell development and differentiation, suggesting their potential roles in T cell programs. However, the key lncRNAs playing crucial roles in memory CD8 T cell establishment remain to be clarified. Through CD8 T cell subsets profiling of lncRNAs, this study found a key lncRNA-Snhg1 with the conserved naive&lt;sup>hi&lt;/sup>-effector&lt;sup>lo&lt;/sup>-memory&lt;sup>hi&lt;/sup> expression pattern in CD8 T cells of both mice and human, that can promote memory formation while impeding effector CD8 in acute viral infection. Further, Snhg1 was found interacting with the conser</pubmed_abstract><journal>Signal transduction and targeted therapy</journal><pubmed_title>The lncRNA Snhg1-Vps13D vesicle trafficking system promotes memory CD8 T cell establishment via regulating the dual effects of IL-7 signaling.</pubmed_title><pmcid>PMC7987995</pmcid><funding_grant_id>31800763</funding_grant_id><funding_grant_id>2016YFA0502202</funding_grant_id><pubmed_authors>Yue S</pubmed_authors><pubmed_authors>Wu J</pubmed_authors><pubmed_authors>Jiang L</pubmed_authors><pubmed_authors>Yang L</pubmed_authors><pubmed_authors>Ni T</pubmed_authors><pubmed_authors>Huang Q</pubmed_authors><pubmed_authors>Zhou X</pubmed_authors><pubmed_authors>Ye L</pubmed_authors><pubmed_authors>Wang P</pubmed_authors><pubmed_authors>Li Z</pubmed_authors><pubmed_authors>Bai Q</pubmed_authors><pubmed_authors>Zhang Y</pubmed_authors><pubmed_authors>Li B</pubmed_authors><pubmed_authors>Wei G</pubmed_authors><pubmed_authors>Hu L</pubmed_authors><pubmed_authors>Wang Z</pubmed_authors><pubmed_authors>Wu Y</pubmed_authors><pubmed_authors>Tian Q</pubmed_authors><pubmed_authors>Zhou J</pubmed_authors></additional><is_claimable>false</is_claimable><name>The lncRNA Snhg1-Vps13D vesicle trafficking system promotes memory CD8 T cell establishment via regulating the dual effects of IL-7 signaling.</name><description>The efficient induction and long-term persistence of pathogen-specific memory CD8 T cells are pivotal to rapidly curb the reinfection. Recent studies indicated that long-noncoding RNAs expression is highly cell- and stage-specific during T cell development and differentiation, suggesting their potential roles in T cell programs. However, the key lncRNAs playing crucial roles in memory CD8 T cell establishment remain to be clarified. Through CD8 T cell subsets profiling of lncRNAs, this study found a key lncRNA-Snhg1 with the conserved naive&lt;sup>hi&lt;/sup>-effector&lt;sup>lo&lt;/sup>-memory&lt;sup>hi&lt;/sup> expression pattern in CD8 T cells of both mice and human, that can promote memory formation while impeding effector CD8 in acute viral infection. Further, Snhg1 was found interacting with the conser</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Mar</publication><modification>2025-04-05T16:17:07.262Z</modification><creation>2022-02-09T15:46:27.457Z</creation></dates><accession>S-EPMC7987995</accession><cross_references><pubmed>33758164</pubmed><doi>10.1038/s41392-021-00492-9</doi></cross_references></HashMap>