Catherine Fust, University of Guelph

Catherine Fust, Caihong Li, and Baozhong Meng, all affiliated with the University of Guelph, Department of Molecular and Cellular Biology.

Expressing & Multiplying

Positive-sense single-stranded RNA viruses such as Grapevine leafroll-associated virus 3 (GLRaV3) replicate their genomes within membrane-bound viral replication complexes (VRCs). The biogenesis of such VRCs is driven by viral "replicase" polyproteins containing several replication-related domains. Past electron microscopy evidence suggests that GLRaV3 forms VRCs from the outer mitochondrial membrane of host grapevine plants. Here, we report the subcellular localization of the replicase polyprotein encoded by GLRaV3 ORF1a (PP1a) towards understanding its putative role in VRC formation. Through confocal laser scanning microscopy analysis of distinct EGFP-tagged PP1a domains, interdomain regions and truncations expressed in model plants, we report the molecular signals responsible for the targeting and association of PP1a to the mitochondria. This signal, located in the "Iceberg" region downstream from the methyltransferase-guanylyltransferase (M/GTase) domain, comprises an amphipathic alpha-helix and a downstream transmembrane domain (TMD). Mutagenesis studies suggest that the polar face of the amphipathic alpha-helix functions as the targeting signal, whereas the non-polar face, together with the TMD, act in membrane-anchoring. When introduced into a GLRaV3 replicon, these mutations impair or abolish viral replication in model plants. Microscopy observations are confirmed through mitochondrial isolation via gradient centrifugation and Western blotting. Structure prediction of the GLRaV3 M/GTase domain and its downstream TMD suggests a putative dodecameric oligomeric state. This dodecamer may gate the neck of GLRaV3 VRCs and contribute to their biogenesis, a hypothesis to be tested in follow-up studies.