<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>6</volume><submitter>Schein A</submitter><pubmed_abstract>Mammalian genomes encode numerous natural antisense long noncoding RNAs (lncRNAs) that regulate gene expression. Recently, an antisense lncRNA to mouse Ubiquitin carboxyl-terminal hydrolase L1 (Uchl1) was reported to increase UCHL1 protein synthesis, representing a new functional class of lncRNAs, designated as SINEUPs, for SINE element-containing translation UP-regulators. Here, we show that an antisense lncRNA to the human protein phosphatase 1 regulatory subunit 12A (PPP1R12A), named as R12A-AS1, which overlaps with the 5' UTR and first coding exon of the PPP1R12A mRNA, functions as a SINEUP, increasing PPP1R12A protein translation in human cells. The SINEUP activity depends on the aforementioned sense-antisense interaction and a free right Alu monomer repeat element at the 3' end of R1</pubmed_abstract><journal>Scientific reports</journal><pagination>33605</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5028707</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Identification of antisense long noncoding RNAs that function as SINEUPs in human cells.</pubmed_title><pmcid>PMC5028707</pmcid><pubmed_authors>Schein A</pubmed_authors><pubmed_authors>Kauppinen S</pubmed_authors><pubmed_authors>Carninci P</pubmed_authors><pubmed_authors>Gustincich S</pubmed_authors><pubmed_authors>Zucchelli S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Identification of antisense long noncoding RNAs that function as SINEUPs in human cells.</name><description>Mammalian genomes encode numerous natural antisense long noncoding RNAs (lncRNAs) that regulate gene expression. Recently, an antisense lncRNA to mouse Ubiquitin carboxyl-terminal hydrolase L1 (Uchl1) was reported to increase UCHL1 protein synthesis, representing a new functional class of lncRNAs, designated as SINEUPs, for SINE element-containing translation UP-regulators. Here, we show that an antisense lncRNA to the human protein phosphatase 1 regulatory subunit 12A (PPP1R12A), named as R12A-AS1, which overlaps with the 5' UTR and first coding exon of the PPP1R12A mRNA, functions as a SINEUP, increasing PPP1R12A protein translation in human cells. The SINEUP activity depends on the aforementioned sense-antisense interaction and a free right Alu monomer repeat element at the 3' end of R1</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Sep</publication><modification>2026-05-03T23:00:37.946Z</modification><creation>2019-03-27T02:24:39Z</creation></dates><accession>S-EPMC5028707</accession><cross_references><pubmed>27646849</pubmed><doi>10.1038/srep33605</doi></cross_references></HashMap>