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Gene Synthesis> | The MYB27 RNAi construct was generated by cloning the C-terminal and 3′UTR sequence of MYB27 into the RNAi vector pDAH2 and subcloned into pART27. Stable transgenic petunia (Petunia hybrida) plants harboring 35Spro:MYB27 or MYB27 RNAi constructs were generated in MP petunia by Agrobacterium tumefaciens–mediated (strain GV3101, MP-90) leaf-disc transformation, essentially as described by Conner et al. (2009). MYB27ΔC was generated using PCR (primers NA192/ NA286; listed in Supplemental Table 4) to remove the EAR motif; MYB27ΔC-VP16 was synthesized by GenScript (www.genscript.com). | Get A Quote |
Plants require sophisticated regulatory mechanisms to ensure the degree of anthocyanin pigmentation is appropriate to myriad developmental and environmental signals. Central to this process are the activity of MYB-bHLH-WD repeat (MBW) complexes that regulate the transcription of anthocyanin genes. In this study, the gene regulatory network that regulates anthocyanin synthesis in petunia (Petunia hybrida) has been characterized. Genetic and molecular evidence show that the R2R3-MYB, MYB27, is an anthocyanin repressor that functions as part of the MBW complex and represses transcription through its C-terminal EAR motif. MYB27 targets both the anthocyanin pathway genes and basic-helix-loop-helix (bHLH) ANTHOCYANIN... More