“…Growth of the clones on the SD/ÀHis/ÀLeu/ÀTrp/ÀAde medium with different concentrations of aureobasidin A (AbA) also indicated that the heterodimers showed the highest stability ( Figure 3a). Previous studies have identified that TsNAC1 could activate TsVP1 expression by recognizing the only CATG (À549 bp) site in the À669 bp to À523 bp region of the TsVP1 promoter (Sun et al, 2010;Liu et al, 2018), and with no T(T/A)AATT site in this region. When the binding sites (orange for CATG, blue for TAAATT) in this region were mutated, four segments with mutated sequences (a, CATGGATAAGCATG; b, CATGGATAAG-TAAATT; c, TAAATTGATAAGTAAATT; d, GATAAG) were produced and connected to the pLacZi as reporters (Figure 3b).…”