Genome-wide binding of SEPALLATA3 and AGAMOUS complexes determined by sequential DNA-affinity purification sequencing.

Examining the average binding intensity for sites common to SEP3–AG, SEP3 Δtet -AG and SEP3 shows that the intensity of binding follows a clear trend with the tetrameric SEP3–AG complex binding most strongly to DNA, followed by the SEP3 Δtet -AG complex and finally by the SEP3 homocomplex, which may be non-physiological as no specific function for the SEP3 homocomplex has been identified (Figure 3B ).

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