AI Article Synopsis

  • * The splicing factor U2AF65B influences the splicing of mRNA surveillance complexes, crucial for maintaining transcript stability in maize.
  • * The sugarcane mosaic virus's protease (NIa-Pro) inhibits U2AF65B's splicing function and its binding to pre-mRNA, disrupting the mRNA surveillance pathway and promoting viral infection.

Article Abstract

The eukaryotic mRNA surveillance pathway, a pivotal guardian of mRNA fidelity, stands at the nexus of diverse biological processes, including antiviral immunity. Despite the recognized function of splicing factors on mRNA fate, the intricate interplay shaping the mRNA surveillance pathway remains elusive. We illustrate that the conserved splicing factor U2 snRNP auxiliary factor large subunit B (U2AF65B) modulates splicing of mRNA surveillance complex, contributing to transcriptomic homeostasis in maize. The functionality of the mRNA surveillance pathway requires ZmU2AF65B-mediated normal splicing of () pre-mRNA, encoding a core factor in this pathway. Intriguingly, sugarcane mosaic virus (SCMV)-coded nuclear inclusion protein a protease (NIa-Pro) hinders the splicing function of ZmU2AF65B. Furthermore, NIa-Pro disrupts ZmU2AF65B binding to pre-mRNA, leading to dysregulated splicing of transcripts and, consequently, impairing mRNA surveillance, thus facilitating viral infection. Together, this study establishes that splicing governs the mRNA surveillance pathway and identifies a pathogenic protein capable of disrupting this regulation to compromise RNA immunity.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11343020PMC
http://dx.doi.org/10.1126/sciadv.adn3010DOI Listing

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