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J Gen Virol 88 (2007), 1005-1015; DOI 10.1099/vir.0.82200-0

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Use of pentapeptide-insertion scanning mutagenesis for functional mapping of the plum pox virus helper component proteinase suppressor of gene silencing

Mark Varrelmann1, Edgar Maiss2, Ruth Pilot1 and Laszlo Palkovics3

1 Department of Crop Science, Section Plant Virology, University of Göttingen, Grisebachstraße 6, D-37077 Göttingen, Germany
2 Institute of Plant Diseases and Plant Protection, University of Hannover, Herrenhaeuser Str. 2, D-30419 Hannover, Germany
3 Department of Plant Pathology, Faculty of Horticultural Science, Corvinus University Budapest, H-1118 Budapest, Hungary

Correspondence
Mark Varrelmann
mvarrel{at}gwdg.de

Helper component proteinase (HC-Pro) of Plum pox virus is a multifunctional potyvirus protein that has been examined intensively. In addition to its involvement in aphid transmission, genome amplification and long-distance movement, it is also one of the better-studied plant virus suppressors of RNA silencing. The first systematic analysis using pentapeptide-insertion scanning mutagenesis of the silencing suppression function of a potyvirus HC-Pro is presented here. Sixty-three in-frame insertion mutants, each containing five extra amino acids inserted randomly within the HC-Pro protein, were analysed for their ability to suppress transgene-induced RNA silencing using Agrobacterium infiltration in transgenic Nicotiana benthamiana plants expressing green fluorescent protein. A functional map was obtained, consisting of clearly defined regions with different classes of silencing-suppression activity (wild-type, restricted and disabled). This map confirmed that the N-terminal part of the protein, which is indispensable for aphid transmission, is dispensable for silencing suppression and supports the involvement of the central region in silencing suppression, in addition to its role in maintenance of genome amplification and synergism with other viruses. Moreover, evidence is provided that the C-terminal part of the protein, previously known to be necessary mainly for proteolytic activity, also participates in silencing suppression. Pentapeptide-insertion scanning mutagenesis has been shown to be a fast and powerful tool to functionally characterize plant virus proteins.




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