Gata3 drives miR-21-5p transcription to mitigate hyperoxia-induced lung injury, independent of CpG Island methylation

Sci Rep. 2025 Jul 4;15(1):23966. doi: 10.1038/s41598-025-09039-2.

Abstract

microRNA-21-5p (miR-21-5p) plays a key anti-apoptotic role in hyperoxia-induced lung injury (HALI), but its regulatory mechanisms are not well understood. This study identified Gata3 as a novel upstream transcription factor that enhanced miR-21-5p expression. Bioinformatic analyses and GEO transcriptomic data revealed a positive correlation between Gata3 and miR-21-5p levels. Notably, the miR-21-5p promoter lacked a CpG island, indicating transcriptional regulation independent of methylation. Gata3 promoted miR-21-5p transcription, reduced apoptosis in alveolar epithelial cells and alleviating HALI. Furthermore, Gata3 overexpression failed to mitigate HALI in miR-21-5p knockout mice, highlighting the critical role of miR-21-5p in Gata3-mediated lung protection. This study uncovered a novel transcriptional mechanism for miRNA regulation, providing valuable insights into the pathogenesis of HALI.

Keywords: Alveolar epithelial cells; Apoptosis; Gata3; Hyperoxia-induced lung injury; miR-21-5p.

MeSH terms

  • Animals
  • Apoptosis / genetics
  • CpG Islands* / genetics
  • DNA Methylation*
  • GATA3 Transcription Factor* / genetics
  • GATA3 Transcription Factor* / metabolism
  • Gene Expression Regulation
  • Humans
  • Hyperoxia* / complications
  • Hyperoxia* / genetics
  • Lung Injury* / etiology
  • Lung Injury* / genetics
  • Lung Injury* / metabolism
  • Lung Injury* / pathology
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • MicroRNAs* / genetics
  • MicroRNAs* / metabolism
  • Promoter Regions, Genetic
  • Transcription, Genetic*

Substances

  • MicroRNAs
  • GATA3 Transcription Factor
  • MIRN21 microRNA, mouse
  • Gata3 protein, mouse