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Priming of Solanum Tuberosum in vitro plants with PVY-specific interfering RNAs activates anti-viral resistance

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Helper component-proteinase (HC-Pro) is a multifunctional suppressor protein synthesized by potato virus Y (PVY), which is able to neutralize the protective mechanisms of RNA interference (RNA-i) in potato plants, thereby causing systemic infection of the host plant and significant damage to the tuber material. This article demonstrates how one of the main functions of HC-Pro, the capture and retention of short interfering RNAs, 21-23 nt in size (siRNA) on the surface of protein subunits, can be used to create virus-resistant potato plants in vitro. The proposed method is based on the selective dissociation of the HC-Pro/siRNA complex from PVY-infected plants and siRNA-priming of healthy plants. Purified preparations of PVY-specific siRNAs were obtained using column gel filtration followed by immunoprecipitation and phenol-chloroform extraction. Injections of siRNA into the leaf plate of virus-free potato microplants, cultivars bred at Amanzholov University, led to a decrease in the accumulation of viral particles in the cytoplasm of plants inoculated with the wild PVY strain and the formation of resistance to PVY for the entire growing season.
Title: Priming of Solanum Tuberosum in vitro plants with PVY-specific interfering RNAs activates anti-viral resistance
Description:
Helper component-proteinase (HC-Pro) is a multifunctional suppressor protein synthesized by potato virus Y (PVY), which is able to neutralize the protective mechanisms of RNA interference (RNA-i) in potato plants, thereby causing systemic infection of the host plant and significant damage to the tuber material.
This article demonstrates how one of the main functions of HC-Pro, the capture and retention of short interfering RNAs, 21-23 nt in size (siRNA) on the surface of protein subunits, can be used to create virus-resistant potato plants in vitro.
The proposed method is based on the selective dissociation of the HC-Pro/siRNA complex from PVY-infected plants and siRNA-priming of healthy plants.
Purified preparations of PVY-specific siRNAs were obtained using column gel filtration followed by immunoprecipitation and phenol-chloroform extraction.
Injections of siRNA into the leaf plate of virus-free potato microplants, cultivars bred at Amanzholov University, led to a decrease in the accumulation of viral particles in the cytoplasm of plants inoculated with the wild PVY strain and the formation of resistance to PVY for the entire growing season.

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