Transcriptome-wide analysis for glucocorticoid receptor-mediated mRNA decay reveals various classes of target transcripts

Mol Cells. 2024 Nov;47(11):100130. doi: 10.1016/j.mocell.2024.100130. Epub 2024 Oct 18.

Abstract

The glucocorticoid receptor (GR) can bind to DNA or RNA, eliciting transcriptional activation/repression or rapid messenger RNA (mRNA) degradation, respectively. Although GR-mediated transcriptional regulation has been well-characterized, the molecular details of rapid mRNA degradation induced by glucocorticoids are not yet fully understood. Here, we demonstrate that glucocorticoid-induced GR-mediated mRNA decay (GMD) takes place in the nucleus and the cytoplasm, acting on pre-mRNAs and mRNAs. We also performed cross-linking and immunoprecipitation coupled with high-throughput sequencing analysis for GMD factors (GR, YBX1, and HRSP12) and mRNA sequencing analysis to identify endogenous GMD substrates. Our comprehensive coupled with high-throughput sequencing and mRNA sequencing analyses reveal that a range of cellular transcripts containing a common binding site for GR, YBX1, and HRSP12 are preferential targets for GMD, suggesting possible new functions of GMD in various biological events.

Keywords: Glucocorticoid; Glucocorticoid receptor; Heat-responsive protein 12; Proline-rich nuclear receptor 2; messenger RNA decay.

MeSH terms

  • Gene Expression Profiling / methods
  • Humans
  • RNA Stability*
  • RNA, Messenger* / genetics
  • RNA, Messenger* / metabolism
  • Receptors, Glucocorticoid* / genetics
  • Receptors, Glucocorticoid* / metabolism
  • Transcriptome
  • Y-Box-Binding Protein 1* / genetics
  • Y-Box-Binding Protein 1* / metabolism

Substances

  • Receptors, Glucocorticoid
  • Y-Box-Binding Protein 1
  • YBX1 protein, human
  • RNA, Messenger