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
JournalNature Communications
DOIs
Publication statusE-pub ahead of print - 16 Dec 2025

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