<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Liu J</submitter><funding>American Heart Association</funding><funding>NHLBI NIH HHS</funding><funding>National Institutes of Health</funding><pagination>333-348.e5</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5567988</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>42(4)</volume><pubmed_abstract>Cardiogenesis processes in human and animals have differential dynamics, suggesting the existence of species-specific regulators during heart development. However, it remains a challenge to discover the human-specific cardiac regulatory genes, given that most coding genes are conserved. Here, we report the identification of a human-specific long noncoding RNA, Heart Brake LncRNA 1 (HBL1), which regulates cardiomyocyte development from human induced pluripotent stem cells (hiPSCs). Overexpression of HBL1 repressed, whereas knockdown and knockout of HBL1 increased, cardiomyocyte differentiation from hiPSCs. HBL1 physically interacted with MIR1 in an AGO2 complex. Disruption of MIR1 binding sites in HBL1 showed an effect similar to that of HBL1 knockout. SOX2 bound to HBL1 promoter and activa</pubmed_abstract><journal>Developmental cell</journal><pubmed_title>HBL1 Is a Human Long Noncoding RNA that Modulates Cardiomyocyte Development from Pluripotent Stem Cells by Counteracting MIR1.</pubmed_title><pmcid>PMC5567988</pmcid><funding_grant_id>1DP2HL127727-01</funding_grant_id><funding_grant_id>17GRNT33440059</funding_grant_id><funding_grant_id>DP2 HL127727</funding_grant_id><funding_grant_id>17POST33460140</funding_grant_id><pubmed_authors>Liu J</pubmed_authors><pubmed_authors>Li Y</pubmed_authors><pubmed_authors>Sheng Y</pubmed_authors><pubmed_authors>Lin B</pubmed_authors><pubmed_authors>Yang L</pubmed_authors></additional><is_claimable>false</is_claimable><name>HBL1 Is a Human Long Noncoding RNA that Modulates Cardiomyocyte Development from Pluripotent Stem Cells by Counteracting MIR1.</name><description>Cardiogenesis processes in human and animals have differential dynamics, suggesting the existence of species-specific regulators during heart development. However, it remains a challenge to discover the human-specific cardiac regulatory genes, given that most coding genes are conserved. Here, we report the identification of a human-specific long noncoding RNA, Heart Brake LncRNA 1 (HBL1), which regulates cardiomyocyte development from human induced pluripotent stem cells (hiPSCs). Overexpression of HBL1 repressed, whereas knockdown and knockout of HBL1 increased, cardiomyocyte differentiation from hiPSCs. HBL1 physically interacted with MIR1 in an AGO2 complex. Disruption of MIR1 binding sites in HBL1 showed an effect similar to that of HBL1 knockout. SOX2 bound to HBL1 promoter and activa</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Aug</publication><modification>2025-04-21T17:47:25.161Z</modification><creation>2019-03-26T23:51:24Z</creation></dates><accession>S-EPMC5567988</accession><cross_references><pubmed>28829943</pubmed><doi>10.1016/j.devcel.2017.07.023</doi></cross_references></HashMap>