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LncRNA CISTR-ACT regulates cell size in human and mouse by guiding FOSL2

  • Katerina Kiriakopulos
  • , Katty Soleimanpour
  • , Brandon J McMurray
  • , Benjamin-Israel Moke
  • , Jordan J Chalmers
  • , Milad Mokhtaridoost
  • , Jeremy D Newton
  • , Taylor De Young
  • , Kate Delfosse
  • , Mai Ahmed
  • , Cassandra J Wong
  • , Sigmar Stricker
  • , Yun Li
  • , Brian J Nieman
  • , Anne-Claude Gingras
  • , Monica J Justice
  • , Julie L Lefebvre
  • , Philipp G Maass

Research output: Journal article (peer-reviewed)Journal article

Abstract

Organisms regulate cell size and shape to function efficiently. Aberrant cell morphogenesis is commonly associated with disease, yet gene-regulatory mechanisms remain unknown. CISTR-ACT was the first lncRNA involved in inter-chromosomal proximities and Mendelian disease, and it is associated with mean corpuscular volume (red blood cell size). Here, functional dissection of CISTR-ACT's DNA- and RNA-encoded mechanisms by in vitro and in vivo perturbations reveals that CISTR-ACT regulates cell size across cell types and species. CISTR-ACT's locus is embedded in a stable inter-chromosomal environment which contains cell size genes that are regulated by CISTR-ACT in trans. CISTR-ACT's RNA also has function and directly interacts with transcription factor FOSL2 to guide its regulation of cell morphogenesis and cell-cell adhesion genes. In the absence of CISTR-ACT, the FOSL2-chromatin binding is perturbed. Our study exemplifies how a functionally conserved lncRNA regulates cell size with multiple modes of action and ultimately contributes to clinically relevant phenotypes.

Original languageEnglish
Article number872
JournalNature Communications
Volume17
Issue number1
Early online date16 Dec 2025
DOIs
Publication statusE-pub ahead of print - 16 Dec 2025

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