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. 2021 Jan 20;10:e62994. doi: 10.7554/eLife.62994

Figure 5. ROS1-directed demethylation is crucial for the DNA binding of WRKY18 and WRKY40 at the RLP43 promoter.

(A) DAP-seq data from O'Malley et al., 2016 showing that WRKY family members are generally sensitive to DNA methylation. Graph representing ratio of binding capacity in DAP versus ampDAP data at regions methylated in Col-0 and for the different transcription factor family members used in this study. (B) The ability of WRKY18 and WRKY40 to bind DNA corresponding to the demethylated region of the RLP43 promoter is abolished in the ros1-3 mutant background. DAP-qPCR analysis at the RLP43 promoter upon pull-down of Col-0 or ros1-3 genomic DNA by GST (negative control), WRKY18-GST or WRKY40-GST. UBQ and bZIP60 served as negative and positive controls, respectively.

Figure 5—source data 1. Original DAP-qPCR data for Figure 5B.

Figure 5.

Figure 5—figure supplement 1. ROS1-directed demethylation is crucial for the binding of WRKY18 and WRKY40 at the RLP43 promoter.

Figure 5—figure supplement 1.

The ability of WRKY18 and WRKY40 to bind DNA corresponding to the demethylated region of the RLP43 promoter is abolished in the ros1-3 mutant background. Second biological replicate of the DAP-qPCR analysis at the RLP43 promoter upon pull-down of Col-0 or ros1-3 genomic DNA by GST (negative control) (upper panel), WRKY18-GST (left panel), or WRKY40-GST (right panel). UBQ and bZIP60 served as negative and positive controls, respectively.
Figure 5—figure supplement 1—source data 1. Original DAP-qPCR data for Figure 5—figure supplement 1.