Maize splicing-mediated mRNA surveillance impeded by sugarcane mosaic virus-coded pathogenic protein NIa-Pro

Author:

Du Kaitong1ORCID,Peng Dezhi1,Wu Jiqiu12ORCID,Zhu Yabing3ORCID,Jiang Tong1,Wang Pei1,Chen Xi1ORCID,Jiang Sanjie3,Li Xiangdong4ORCID,Cao Zhiyan5ORCID,Fan Zaifeng1ORCID,Zhou Tao1ORCID

Affiliation:

1. State Key Laboratory of Maize Bio-breeding and Department of Plant Pathology, China Agricultural University, Beijing 100193, China.

2. Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, Netherlands.

3. BGI Tech Solutions Co. Ltd. BGI-Shenzhen, Shenzhen, China.

4. College of Plant Protection, Shandong Agricultural University, Taian 271018, Shandong, China.

5. College of Plant Protection, Hebei Agricultural University, Baoding 071001, Hebei, China.

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 upstream frameshift 3 ( ZmUPF3 ) 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 ZmUPF3 pre-mRNA, leading to dysregulated splicing of ZmUPF3 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.

Publisher

American Association for the Advancement of Science (AAAS)

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