Yang Guangyan, Xue Zhaolong, Lin-Wang Kui, Chen Guosong, Zhao Yongqi, Chang Yaojun, Xu Shaozhuo, Sun Manyi, Xue Cheng, Li Jiaming, Allan Andrew C, Espley Richard V, Wu Jun
College of Horticulture, State Key Laboratory of Crop Genetics and Germplasm Enhancement, Nanjing Agricultural University, Nanjing, 210095, China.
Zhongshan Biological Breeding Laboratory, Nanjing, 210014, Jiangsu, China.
Mol Hortic. 2024 Jul 1;4(1):26. doi: 10.1186/s43897-024-00102-6.
The color of red-skinned pear (Pyrus spp.) is primarily attributed to accumulation of anthocyanins, which provide nutritional benefits for human health and are closely associated with the commercial value of fruits. Here, we reported the functional characterization of a R2R3-MYB repressor PyMYB107, which forms an 'activator-repressor' loop to control anthocyanin accumulation in the red-skinned pear. PyMYB107 overexpression inhibited anthocyanin biosynthesis in both pear calli and fruits, while virus-induced gene silencing of PyMYB107 increased anthocyanin accumulation in pear fruits. Furthermore, ectopic expression of PyMYB107 decreased anthocyanin accumulation in tomato, strawberry and tobacco. PyMYB107 can competitively bind to PybHLH3 with PyMYB10/MYB114, thereby suppressing the transcriptional activation of key anthocyanin biosynthesis genes, PyANS and PyUFGT. Site-directed mutagenesis showed that mutations within the R3 domain and EAR motif of PyMYB107 eliminated its repressive activity. Additionally, PyMYB107 exhibited a comparable expression pattern to PyMYB10/MYB114 and was transcriptionally activated by them. Our finding advanced comprehension of the repression mechanism underlying anthocyanin accumulation, providing valuable molecular insights into improving quality of pear fruits.
红皮梨(梨属)的颜色主要归因于花青素的积累,花青素对人体健康有益,且与果实的商业价值密切相关。在此,我们报道了一种R2R3-MYB抑制因子PyMYB107的功能特性,它形成一个“激活因子-抑制因子”环来控制红皮梨中花青素的积累。PyMYB107过表达抑制了梨愈伤组织和果实中花青素的生物合成,而PyMYB107的病毒诱导基因沉默增加了梨果实中花青素的积累。此外,PyMYB107的异位表达降低了番茄、草莓和烟草中花青素的积累。PyMYB107可以与PyMYB10/MYB114竞争性结合PybHLH3,从而抑制关键花青素生物合成基因PyANS和PyUFGT的转录激活。定点诱变表明,PyMYB107的R3结构域和EAR基序内的突变消除了其抑制活性。此外,PyMYB107表现出与PyMYB10/MYB114相似的表达模式,并受到它们的转录激活。我们的发现加深了对花青素积累抑制机制的理解,为改善梨果实品质提供了有价值的分子见解。