<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ma W</submitter><funding>National Natural Science Foundation of China</funding><pagination>42</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7045492</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>19(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>The CDKN2A/B locus contains crucial tumor suppressors and a lncRNA gene ANRIL. However, the mechanisms that coordinately regulate their expression levels are not clear.&lt;h4>Methods&lt;/h4>Novel RNAs transcribed from the CDKN2A gene were screened by CDKN2A-specific RNA capture deep-sequencing and confirmed by Northern blotting and clone-sequencing. Long non-coding RNA (lncRNA) binding proteins were characterized by RNA pull-down combined with mass spectrometry and RNA immunoprecipitation. LncRNA functions in human cells were studied using a set of biological assays in vitro and in vivo.&lt;h4>Results&lt;/h4>We characterized a novel lncRNA, P14AS with its promoter in the antisense strand of the fragment near CDKN2A exon 1b in human cells. The mature P14AS is a three-exon linear cyto</pubmed_abstract><journal>Molecular cancer</journal><pubmed_title>Characterization of novel LncRNA P14AS as a protector of ANRIL through AUF1 binding in human cells.</pubmed_title><pmcid>PMC7045492</pmcid><funding_grant_id>91640108</funding_grant_id><pubmed_authors>Deng D</pubmed_authors><pubmed_authors>Gu L</pubmed_authors><pubmed_authors>Qiao J</pubmed_authors><pubmed_authors>Ma W</pubmed_authors><pubmed_authors>Zhou J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Characterization of novel LncRNA P14AS as a protector of ANRIL through AUF1 binding in human cells.</name><description>&lt;h4>Background&lt;/h4>The CDKN2A/B locus contains crucial tumor suppressors and a lncRNA gene ANRIL. However, the mechanisms that coordinately regulate their expression levels are not clear.&lt;h4>Methods&lt;/h4>Novel RNAs transcribed from the CDKN2A gene were screened by CDKN2A-specific RNA capture deep-sequencing and confirmed by Northern blotting and clone-sequencing. Long non-coding RNA (lncRNA) binding proteins were characterized by RNA pull-down combined with mass spectrometry and RNA immunoprecipitation. LncRNA functions in human cells were studied using a set of biological assays in vitro and in vivo.&lt;h4>Results&lt;/h4>We characterized a novel lncRNA, P14AS with its promoter in the antisense strand of the fragment near CDKN2A exon 1b in human cells. The mature P14AS is a three-exon linear cyto</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Feb</publication><modification>2026-04-16T19:07:09.98Z</modification><creation>2020-05-22T11:44:46Z</creation></dates><accession>S-EPMC7045492</accession><cross_references><pubmed>32106863</pubmed><doi>10.1186/s12943-020-01150-4</doi></cross_references></HashMap>