<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Yari H</submitter><funding>Department of Health | National Health and Medical Research Council</funding><pagination>5334</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6877513</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>10(1)</volume><pubmed_abstract>Protein products of the regenerating islet-derived (REG) gene family are important regulators of many cellular processes. Here we functionally characterise a non-protein coding product of the family, the long noncoding RNA (lncRNA) REG1CP that is transcribed from a DNA fragment at the family locus previously thought to be a pseudogene. REG1CP forms an RNA-DNA triplex with a homopurine stretch at the distal promoter of the REG3A gene, through which the DNA helicase FANCJ is tethered to the core promoter of REG3A where it unwinds double stranded DNA and facilitates a permissive state for glucocorticoid receptor α (GRα)-mediated REG3A transcription. As such, REG1CP promotes cancer cell proliferation and tumorigenicity and its upregulation is associated with poor outcome of patients. REG1CP is</pubmed_abstract><journal>Nature communications</journal><pubmed_title>LncRNA REG1CP promotes tumorigenesis through an enhancer complex to recruit FANCJ helicase for REG3A transcription.</pubmed_title><pmcid>PMC6877513</pmcid><funding_grant_id>APP1147271</funding_grant_id><funding_grant_id>APP1162753</funding_grant_id><pubmed_authors>Zhang YY</pubmed_authors><pubmed_authors>Yan XG</pubmed_authors><pubmed_authors>Thorne RF</pubmed_authors><pubmed_authors>Xi Y</pubmed_authors><pubmed_authors>Tabatabaee H</pubmed_authors><pubmed_authors>La T</pubmed_authors><pubmed_authors>Guo ST</pubmed_authors><pubmed_authors>Yari H</pubmed_authors><pubmed_authors>Liu T</pubmed_authors><pubmed_authors>Teng L</pubmed_authors><pubmed_authors>Farrelly M</pubmed_authors><pubmed_authors>Zhang XD</pubmed_authors><pubmed_authors>Liu GZ</pubmed_authors><pubmed_authors>Scott R</pubmed_authors><pubmed_authors>Liang J</pubmed_authors><pubmed_authors>Feng YC</pubmed_authors><pubmed_authors>Gao W</pubmed_authors><pubmed_authors>Yang RH</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Zhang C</pubmed_authors><pubmed_authors>Wu Y</pubmed_authors><pubmed_authors>Wang FH</pubmed_authors><pubmed_authors>Jin L</pubmed_authors></additional><is_claimable>false</is_claimable><name>LncRNA REG1CP promotes tumorigenesis through an enhancer complex to recruit FANCJ helicase for REG3A transcription.</name><description>Protein products of the regenerating islet-derived (REG) gene family are important regulators of many cellular processes. Here we functionally characterise a non-protein coding product of the family, the long noncoding RNA (lncRNA) REG1CP that is transcribed from a DNA fragment at the family locus previously thought to be a pseudogene. REG1CP forms an RNA-DNA triplex with a homopurine stretch at the distal promoter of the REG3A gene, through which the DNA helicase FANCJ is tethered to the core promoter of REG3A where it unwinds double stranded DNA and facilitates a permissive state for glucocorticoid receptor α (GRα)-mediated REG3A transcription. As such, REG1CP promotes cancer cell proliferation and tumorigenicity and its upregulation is associated with poor outcome of patients. REG1CP is</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Nov</publication><modification>2026-06-17T06:53:30.286Z</modification><creation>2026-06-17T03:10:28.287Z</creation></dates><accession>S-EPMC6877513</accession><cross_references><pubmed>31767869</pubmed><doi>10.1038/s41467-019-13313-z</doi></cross_references></HashMap>