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Article: Identification of circular RNAs regulating cardiomyocyte proliferation in neonatal pig hearts

TitleIdentification of circular RNAs regulating cardiomyocyte proliferation in neonatal pig hearts
Authors
Issue Date25-Jun-2024
PublisherAmerican Society for Clinical Investigation
Citation
JCI Insight, 2024, v. 9, n. 15 How to Cite?
Abstract

Little is known about the expression patterns and functions of circular RNAs (circRNAs) in the heart of large mammals. In this study, we examined the expression profiles of circRNAs, microRNAs (miRNAs), and messenger RNAs (mRNAs) in neonatal pig hearts. Pig heart samples collected on postnatal days 1 (P1), 3 (P3), 7 (P7), and 28 (P28) were sent for total RNA sequencing. Our data revealed a total of 7,000 circRNAs in the 24 pig hearts. Pathway enrichment analysis of hallmark gene sets demonstrated that differentially expressed circRNAs were engaged in different pathways. The most significant difference was observed between P1 and the other 3 groups (P3, P7, and P28) in pathways related to cell cycle and muscle development. Out of the 10 circRNAs that were validated through real-time quantitative PCR to verify their expression, 6 exhibited significant effects on cell cycle activity in human induced pluripotent stem cell–derived cardiomyocytes following small interfering RNA–mediated knockdown. circRNA-miRNA-mRNA networks were constructed to understand the potential mechanisms of circRNAs in the heart. In conclusion, our study provided a data set for exploring the roles of circRNAs in pig hearts. In addition, we identified several circRNAs that regulate cardiomyocyte cell cycle.


Persistent Identifierhttp://hdl.handle.net/10722/346236
ISSN
2023 Impact Factor: 6.3
2023 SCImago Journal Rankings: 2.970

 

DC FieldValueLanguage
dc.contributor.authorTang, Ling-
dc.contributor.authorNyarige, Verah-
dc.contributor.authorLi, Pengsheng-
dc.contributor.authorWang, Junwen-
dc.contributor.authorZhu, Wuqiang-
dc.date.accessioned2024-09-12T00:31:01Z-
dc.date.available2024-09-12T00:31:01Z-
dc.date.issued2024-06-25-
dc.identifier.citationJCI Insight, 2024, v. 9, n. 15-
dc.identifier.issn2379-3708-
dc.identifier.urihttp://hdl.handle.net/10722/346236-
dc.description.abstract<p>Little is known about the expression patterns and functions of circular RNAs (circRNAs) in the heart of large mammals. In this study, we examined the expression profiles of circRNAs, microRNAs (miRNAs), and messenger RNAs (mRNAs) in neonatal pig hearts. Pig heart samples collected on postnatal days 1 (P1), 3 (P3), 7 (P7), and 28 (P28) were sent for total RNA sequencing. Our data revealed a total of 7,000 circRNAs in the 24 pig hearts. Pathway enrichment analysis of hallmark gene sets demonstrated that differentially expressed circRNAs were engaged in different pathways. The most significant difference was observed between P1 and the other 3 groups (P3, P7, and P28) in pathways related to cell cycle and muscle development. Out of the 10 circRNAs that were validated through real-time quantitative PCR to verify their expression, 6 exhibited significant effects on cell cycle activity in human induced pluripotent stem cell–derived cardiomyocytes following small interfering RNA–mediated knockdown. circRNA-miRNA-mRNA networks were constructed to understand the potential mechanisms of circRNAs in the heart. In conclusion, our study provided a data set for exploring the roles of circRNAs in pig hearts. In addition, we identified several circRNAs that regulate cardiomyocyte cell cycle.</p>-
dc.languageeng-
dc.publisherAmerican Society for Clinical Investigation-
dc.relation.ispartofJCI Insight-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.titleIdentification of circular RNAs regulating cardiomyocyte proliferation in neonatal pig hearts-
dc.typeArticle-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1172/jci.insight.175625-
dc.identifier.scopuseid_2-s2.0-85200939169-
dc.identifier.volume9-
dc.identifier.issue15-
dc.identifier.eissn2379-3708-
dc.identifier.issnl2379-3708-

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