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. 2019 Nov 27;19:522. doi: 10.1186/s12870-019-2139-6

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© The Author(s). 2019

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. 6 — Functional analysis of rose transcription factor gene RcWRKY41. (A) Compromised B. cinerea resistance symptoms on rose petal disks upon the silencing of RcWRKY41, shown at 60 hpi (hours post inoculation). A recombinant tobacco rattle virus (TRV) targeting RcWRKY41 (TRV-RcWRKY41) was used for the gene silencing, and an empty TRV (TRV-00) was used as the control. (B) Quantification of the average diameter of the disease lesions on the control and RcWRKY41-silenced petals at 60 hpi. Error bars = standard deviation. The statistical analysis was performed using a Student’s t-test; ** P < 0.01. (C) Quantification of RcWRKY41 expression in TRV-RcWRKY41-inoculated petal discs relative to that in the control