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An i-motif-regulated enhancer, eRNA and adjacent lncRNA affect Lhb expression through distinct mechanisms in a sex-specific context

Tal Refael, Maya Sudman, Gil Golan, Lilach Pnueli, Sujay Naik, Ella Preger-Ben Noon, Arnon Henn, Ariel Kaplan, Philippa Melamed

Research output: Contribution to journalArticlepeer-review

Abstract

Genome-wide studies have demonstrated regulatory roles for diverse non-coding elements, but their precise and interrelated functions have often remained enigmatic. Addressing the need for mechanistic insight, we studied their roles in expression of Lhb which encodes the pituitary gonadotropic hormone that controls reproduction. We identified a bi-directional enhancer in gonadotrope-specific open chromatin, whose functional eRNA (eRNA2) supports permissive chromatin at the Lhb locus. The central untranscribed region of the enhancer contains an iMotif (iM), and is bound by Hmgb2 which stabilizes the iM and directs transcription specifically towards the functional eRNA2. A distinct downstream lncRNA, associated with an inducible G-quadruplex (G4) and iM, also facilitates Lhb expression, following its splicing in situ. GnRH activates Lhb transcription and increased levels of all three RNAs, eRNA2 showing the highest response, while estradiol, which inhibits Lhb, repressed levels of eRNA2 and the lncRNA. The levels of these regulatory RNAs and Lhb mRNA correlate highly in female mice, though strikingly not in males, suggesting a female-specific function. Our findings, which shed new light on the workings of non-coding elements and non-canonical DNA structures, reveal novel mechanisms regulating transcription which have implications not only in the central control of reproduction but also for other inducible genes.

Original languageEnglish
Article number361
Pages (from-to)361
JournalCellular and Molecular Life Sciences
Volume81
Issue number1
DOIs
StatePublished - 19 Aug 2024

Keywords

  • Animals
  • Biological sciences
  • Chromatin conformation
  • Chromatin/metabolism
  • Enhancer Elements, Genetic
  • Epigenetic
  • Female
  • G-Quadruplexes
  • Gene Expression Regulation
  • Histone
  • Humans
  • Luteinizing Hormone, beta Subunit/metabolism
  • Luteinizing hormone
  • Male
  • Mice
  • Mice, Inbred C57BL
  • RNA, Long Noncoding/genetics
  • Steroid

All Science Journal Classification (ASJC) codes

  • Cellular and Molecular Neuroscience
  • Molecular Medicine
  • Molecular Biology
  • Cell Biology
  • Pharmacology

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