<p>Organisms regulate cell size and shape to function efficiently. Aberrant cell morphogenesis is commonly associated with disease, yet gene-regulatory mechanisms remain unknown. <i>CISTR-ACT</i> was the first lncRNA involved in <i>inter-</i>chromosomal proximities and Mendelian disease, and it&#xa0;is associated with mean corpuscular volume (red blood cell size). Here, functional dissection of <i>CISTR-ACT</i>’s DNA- and RNA-encoded mechanisms by in vitro and in vivo perturbations reveals that <i>CISTR-ACT</i> regulates cell size across cell types and species. <i>CISTR-ACT</i>’s locus is embedded in a stable <i>inter-</i>chromosomal environment which contains cell size genes that are regulated by <i>CISTR-ACT</i> in trans. <i>CISTR-ACT</i>’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 <i>CISTR-ACT</i>, 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.</p>

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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

摘要

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.