Go to The Journal of Clinical Investigation
  • About
  • Editors
  • Consulting Editors
  • For authors
  • Publication ethics
  • Publication alerts by email
  • Transfers
  • Advertising
  • Job board
  • Contact
  • Physician-Scientist Development
  • Current issue
  • Past issues
  • By specialty
    • COVID-19
    • Cardiology
    • Immunology
    • Metabolism
    • Nephrology
    • Oncology
    • Pulmonology
    • All ...
  • Videos
  • Collections
    • In-Press Preview
    • Resource and Technical Advances
    • Clinical Research and Public Health
    • Research Letters
    • Editorials
    • Perspectives
    • Physician-Scientist Development
    • Reviews
    • Top read articles

  • Current issue
  • Past issues
  • Specialties
  • In-Press Preview
  • Resource and Technical Advances
  • Clinical Research and Public Health
  • Research Letters
  • Editorials
  • Perspectives
  • Physician-Scientist Development
  • Reviews
  • Top read articles
  • About
  • Editors
  • Consulting Editors
  • For authors
  • Publication ethics
  • Publication alerts by email
  • Transfers
  • Advertising
  • Job board
  • Contact
Identification of circular RNAs regulating cardiomyocyte proliferation in neonatal pig hearts
Ling Tang, Verah Nyarige, Pengsheng Li, Junwen Wang, Wuqiang Zhu
Ling Tang, Verah Nyarige, Pengsheng Li, Junwen Wang, Wuqiang Zhu
View: Text | PDF
Research Article Cardiology

Identification of circular RNAs regulating cardiomyocyte proliferation in neonatal pig hearts

  • Text
  • PDF
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.

Authors

Ling Tang, Verah Nyarige, Pengsheng Li, Junwen Wang, Wuqiang Zhu

×

Figure 1

Differentially expressed circRNAs in neonatal pig hearts and functional enrichment analysis.

Options: View larger image (or click on image) Download as PowerPoint
Differentially expressed circRNAs in neonatal pig hearts and functional ...
(A–D) A heatmap of differentially expressed and cell cycle–related circRNAs depicting expression patterns from various comparisons including P1 versus P3 (A), P1 versus P7 (B), P1 versus P28 (C), and P1 versus P3, P7, and P28 (D). circRNAs with high expression values are colored in dark green while those with low expression values are in dark pink. (E–H) Pathway enrichment analysis plots of top ranked cell cycle–related hallmark pathways from various comparisons including (E) P1 versus P3, (F) P1 versus P7, (G) P1 versus P28, and (H) P1 versus P3, P7, and P28. Panels A–H were generated using circRNA data from 35 batch-corrected RNA samples obtained from 24 pig hearts sequenced by CD Genomics Inc. (“cd”), and Novogene Inc. (“nv1” and “nv2”).

Copyright © 2026 American Society for Clinical Investigation
ISSN 2379-3708

Sign up for email alerts