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. 2004 Mar;134(3):1069–1079. doi: 10.1104/pp.103.030577

Figure 5.

Figure 5.

ZmMADS2 forms homodimers in the yeast two-hybrid system. Three independent clones were each pipetted on agar plates containing full medium without selection (a); selection medium without His, Trp, Lys, and Ura with 300 μg mL-1 Zeocin (b), and the β-galactosidase assay (c). Top row, ZmMADS2 fused to the LexA BD (DNA-binding domain), bait. Second row, ZmMADS2 fused to the B42 activation domain (AD), prey. Third row, ZmMADS2 fused to LexA BD (bait) and ZmMADS2 fused to B42 AD (prey). Fourth row, Fos fused to LexA BD (bait) and Jun fused to B42 AD (prey) as positive control. Fifth row, Fos fused to LexA BD (prey) and Lamin fused to B42 AD (prey) as a negative control.