College of Plant Protection; Yángzhōu University; Yángzhōu, Jiāngsū Province; China.
Integrated Research Facility at Fort Detrick; National Institute of Allergy and Infectious Diseases, National Institutes of Health, Fort Detrick; Frederick, Maryland; United States of America.
PLoS Pathog. 2024 Mar 20;20(3):e1012112. doi: 10.1371/journal.ppat.1012112. eCollection 2024 Mar.
Viruses are encapsidated mobile genetic elements that rely on host cells for replication. Several cytoplasmic RNA viruses synthesize proteins and/or RNAs that translocate to infected cell nuclei. However, the underlying mechanisms and role(s) of cytoplasmic-nuclear trafficking are unclear. We demonstrate that infection of small brown planthoppers with rice stripe virus (RSV), a negarnaviricot RNA virus, results in K63-linked polyubiquitylation of RSV's nonstructural protein 3 (NS3) at residue K127 by the RING ubiquitin ligase (E3) LsRING. In turn, ubiquitylation leads to NS3 trafficking from the cytoplasm to the nucleus, where NS3 regulates primary miRNA pri-miR-92 processing through manipulation of the microprocessor complex, resulting in accumulation of upregulated miRNA lst-miR-92. We show that lst-miR-92 regulates the expression of fibrillin 2, an extracellular matrix protein, thereby increasing RSV loads. Our results highlight the manipulation of intranuclear, cytoplasmic, and extracellular components by an RNA virus to promote its own replication in an insect vector.
病毒是包裹在囊膜中的可移动遗传因子,依赖宿主细胞进行复制。几种细胞质 RNA 病毒合成蛋白质和/或 RNA,这些物质易位到感染的细胞细胞核中。然而,细胞质-核易位的潜在机制和作用尚不清楚。我们证明,感染水稻条纹病毒(RSV)会导致 RSV 的非结构蛋白 3(NS3)在残基 K127 处发生 K63 连接的多泛素化,由 RING 泛素连接酶(E3)LsRING 介导。反过来,泛素化导致 NS3 从细胞质向细胞核易位,NS3 通过操纵微处理器复合物来调节初级 miRNA pri-miR-92 的加工,导致上调 miRNA lst-miR-92 的积累。我们表明 lst-miR-92 调节细胞外基质蛋白纤维蛋白 2 的表达,从而增加 RSV 的载量。我们的结果强调了 RNA 病毒对细胞核内、细胞质和细胞外成分的操纵,以促进其在昆虫载体中的自身复制。