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. Author manuscript; available in PMC: 2021 Aug 25.
Published in final edited form as: Nat Plants. 2021 Feb 25;7(3):342–352. doi: 10.1038/s41477-021-00863-8

Extended Data Fig. 3. TET8 and PEN1 localization.

Extended Data Fig. 3

a, Confocal microscopy images of TET8-YFP and ARA6-CFP at B. cinerea infection site on N. benthamiana. TET8-YFP was partially co-localized with ARA6-CFP signals. b, Fluorescent intensity was quantified for the images used in (a). Transections used for fluorescence intensity measurements are indicated by blue lines. Green and red lines represent histograms of ARA6-CFP and TET8-YFP fluorescent intensities, respectively. c, Confocal microscopy images of CFP-PEN1 and ARA6-YFP at the B. cinerea infection site on N. benthamiana. CFP-PEN1 and ARA6-YFP do not co-localize with ARA6-YFP signals. d, Fluorescence intensity was quantified for the images used in (c). Transections used for fluorescence intensity measurements are indicated by blue lines. Green and red lines represent histograms of CFP-PEN1 and ARA6-YFP fluorescent intensities, respectively. Scale bars, 10 μm.