<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>17(4)</volume><submitter>He P</submitter><pubmed_abstract>Endogenous bornavirus-like nucleoprotein elements (EBLNs) have been discovered in the genomes of various animals including humans, whose functions have been seldom studied. To explore the biological functions of human EBLNs, we constructed a lentiviral vector expressing a short-hairpin RNA against human EBLN1, which successfully inhibited EBLN1 expression by above 80% in infected human oligodendroglia cells (OL cells). We found that EBLN1 silencing suppressed cell proliferation, induced G2/M phase arrest, and promoted apoptosis in OL cells. Gene expression profiling demonstrated that 1067 genes were up-regulated, and 2004 were down-regulated after EBLN1 silencing. The top 10 most upregulated genes were PI3, RND3, BLZF1, SOD2, EPGN, SBSN, INSIG1, OSMR, CREB3L2, and MSMO1, and the top 10 mos</pubmed_abstract><journal>International journal of molecular sciences</journal><pagination>435</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4848891</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Knock-Down of Endogenous Bornavirus-Like Nucleoprotein 1 Inhibits Cell Growth and Induces Apoptosis in Human Oligodendroglia Cells.</pubmed_title><pmcid>PMC4848891</pmcid><pubmed_authors>Sun L</pubmed_authors><pubmed_authors>Guo Y</pubmed_authors><pubmed_authors>Zhang H</pubmed_authors><pubmed_authors>Zhang L</pubmed_authors><pubmed_authors>Liu S</pubmed_authors><pubmed_authors>Xu X</pubmed_authors><pubmed_authors>Xie P</pubmed_authors><pubmed_authors>Zhu D</pubmed_authors><pubmed_authors>He P</pubmed_authors><pubmed_authors>Zhou J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Knock-Down of Endogenous Bornavirus-Like Nucleoprotein 1 Inhibits Cell Growth and Induces Apoptosis in Human Oligodendroglia Cells.</name><description>Endogenous bornavirus-like nucleoprotein elements (EBLNs) have been discovered in the genomes of various animals including humans, whose functions have been seldom studied. To explore the biological functions of human EBLNs, we constructed a lentiviral vector expressing a short-hairpin RNA against human EBLN1, which successfully inhibited EBLN1 expression by above 80% in infected human oligodendroglia cells (OL cells). We found that EBLN1 silencing suppressed cell proliferation, induced G2/M phase arrest, and promoted apoptosis in OL cells. Gene expression profiling demonstrated that 1067 genes were up-regulated, and 2004 were down-regulated after EBLN1 silencing. The top 10 most upregulated genes were PI3, RND3, BLZF1, SOD2, EPGN, SBSN, INSIG1, OSMR, CREB3L2, and MSMO1, and the top 10 mos</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Mar</publication><modification>2026-05-30T11:18:46.438Z</modification><creation>2019-03-27T02:12:37Z</creation></dates><accession>S-EPMC4848891</accession><cross_references><pubmed>27023521</pubmed><doi>10.3390/ijms17040435</doi></cross_references></HashMap>