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. 2016 Feb 2;67(6):1795–1804. doi: 10.1093/jxb/erv569

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© The Author 2016. Published by Oxford University Press on behalf of the Society for Experimental Biology.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

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Fig. 3. — Effect of DPI on promoter activity of MYB14 in response to UV-C. Values give fold induction levels of promoter activity in the presence of UV-C and UV-C with NADPH oxidase inhibitor (DPI) relative to the respective control (C) (promoter activity without any treatments). +UV-C: fold induction of promoter activity for 3h after the UV-C irradiation for 2min; +UV-C+DPI: fold induction of promoter activity for 3h after the addition of DPI (10 μM) and UV-C for 2min. Values were calibrated against the co-bombarded Renilla luciferase plasmid pRluc as an internal standard. * indicate differences that are statistically significant on the P <0.05 level and ** indicate P <0.01 level. Mean values and standard errors from three independent experimental series.