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. 2017 Jul 17;14:129. doi: 10.1186/s12985-017-0803-8

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© The Author(s). 2017

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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Fig. 9 — Expression levels of selected target potato coding transcripts commonly targeted by Potato virus Y (PVY)-derived small RNAs (vsiRNAs) derived from tobacco veinal-necrotic strain (PVY-N), necrosis tuber-necrotic strain (PVY-NTN) and ordinary strain (PVY-O). In potato plants (Russet Burbank) infected with PVY-NTN, the expression levels of PGSC0003DMT400072865 - protein kinase splA, PGSC0003DMT400074377 - heat shock protein-90 (HSP-90), PGSC0003DMT400073246 - aquaporin NIP1–1, PGSC0003DMT400074517 - β-1,3 galactosyltransferase 2, PGSC0003DMT400075191 - Histone-lysine N methyltransferase, PGSC0003DMT400002313 - BTB/POZ domain containing protein, PGSC0003DMT400060832 - casein kinase, PGSC0003DMT400077373 - Gamma glutamyl transferase 1, PGSC0003DMT400026847 - VPS51/VPS67 family protein and PGSC0003DMT400018414 - phosphoglycerate mutase were downregulated. The elongation factor 1-alpha (ef1alpha) and actin genes were used for normalization. Error bars indicate the standard deviations of qRT-PCR signals (n = 3)