“…In this respect, MdMYBA, MdMYB1, MdMYB9, MdMYB10, MdMYB110a, and MdMYB11 are all identified R2R3-MYBs that regulate anthocyanin biosynthesis in the peel and flesh of apples: MdMYB1, MdMYB10, and MdMYBA have higher homologies and similar functions for activating LBGs; MdMYB110a is mainly responsible for anthocyanin accumulation of red fleshes in fruits; MdMYB9 and MdMYB11 have a relatively distant relationship to the aforesaid MdMYBs, and the module mechanism of them is to respond to jasmonic acid induction and then activate EBGs such as MdCHS , MdCHI , and MdF3H , as well as several LBGs such as MdANS , MdDFR , and MdANR ; both MdMYBL2 and MdMYB6 could inhibit anthocyanin biosynthesis via different mechanisms, whereby the former functions as a repressor interacting with MdbHLH3 to indirectly inhibit the upregulation of MdMYB10 , MdbHLH3 , MdDFR , and MdUFGT , while MdMYB6 could inhibit anthocyanin biosynthesis by regulating MdANS and MdGSTF12 during the coloration of developing fruits ( Naing and Kim, 2018 ; Wang et al, 2019 ; Xu H. et al, 2020 ). The expression levels of F3H , UFGT2 , MYB10 , and bHLH3 might be critical and coordinated for the anthocyanin synthesis in pear fruits’ development, whereas GST and key light-responsive genes, such as COP1 , PIF3.1 , and PIF3.2 , played limited roles in its regulation ( Wu et al, 2019 ). In vegetable crops, studies pay particular attention to either vegetative developing or the fruit development.…”