NONO enhances mRNA processing of super-enhancer-associated GATA2 and HAND2 genes in neuroblastoma

  • EMBO Rep. 2022 Nov 23;e54977. doi: 10.15252/embr.202254977.
Song Zhang  1 Jack Al Cooper  1 Yee Seng Chong  2 Alina Naveed  1 Chelsea Mayoh  3  4  5 Nisitha Jayatilleke  3  4 Tao Liu  3  4 Sebastian Amos  1 Simon Kobelke  1 Andrew C Marshall  2 Oliver Meers  1 Yu Suk Choi  1 Charles S Bond  2 Archa H Fox  1  2
Affiliations
  • 1. School of Human Sciences, The University of Western Australia, Crawley, WA, Australia.
  • 2. School of Molecular Sciences, The University of Western Australia, Crawley, WA, Australia.
  • 3. Children's Cancer Institute Australia, Randwick, NSW, Australia.
  • 4. Centre for Childhood Cancer Research, UNSW Sydney, Kensington, NSW, Australia.
  • 5. School of Women's and Children's Health, UNSW Sydney, Kensington, NSW, Australia.
Abstract

High-risk neuroblastoma patients have poor survival rates and require better therapeutic options. High expression of a multifunctional DNA and RNA-binding protein, NONO, in neuroblastoma is associated with poor patient outcome; however, there is little understanding of the mechanism of NONO-dependent oncogenic gene regulatory activity in neuroblastoma. Here, we used cell imaging, biochemical and genome-wide molecular analysis to reveal complex NONO-dependent regulation of gene expression. NONO forms RNA- and DNA-tethered condensates throughout the nucleus and undergoes phase separation in vitro, modulated by nucleic acid binding. CLIP analyses show that NONO mainly binds to the 5' end of pre-mRNAs and modulates pre-mRNA processing, dependent on its RNA-binding activity. NONO regulates super-enhancer-associated genes, including HAND2 and GATA2. Abrogating NONO RNA binding, or phase separation activity, results in decreased expression of HAND2 and GATA2. Thus, future development of agents that target RNA-binding activity of NONO may have therapeutic potential in this Cancer context.

Keywords
DBHS; RNA binding; neuroblastoma; phase separation; super-enhancer.
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