Cao Yunlin, Jia Huimin, Xing Mengyun, Jin Rong, Grierson Donald, Gao Zhongshan, Sun Chongde, Chen Kunsong, Xu Changjie, Li Xian
Zhejiang Provincial Key Laboratory of Horticultural Plant Integrative Biology, Zhejiang University, Hangzhou, China.
The State Agriculture Ministry Laboratory of Horticultural Plant Growth, Development and Quality Improvement, Zhejiang University, Hangzhou, China.
Front Plant Sci. 2021 Jun 24;12:691384. doi: 10.3389/fpls.2021.691384. eCollection 2021.
Chinese bayberry (), the most economically important fruit tree in the Myricaceae family, is a rich source of natural flavonoids. Recently the Chinese bayberry genome has been sequenced, and this provides an opportunity to investigate the organization and evolutionary characteristics of genes from a whole genome view. In the present study, we performed the genome-wide analysis of genes in Chinese bayberry and identified 174 MrMYB transcription factors (TFs), including 122 R2R3-MYBs, 43 1R-MYBs, two 3R-MYBs, one 4R-MYB, and six atypical MYBs. Collinearity analysis indicated that both syntenic and tandem duplications contributed to expansion of the gene family. Analysis of transcript levels revealed the distinct expression patterns of different genes, and those which may play important roles in leaf and flower development. Through phylogenetic analysis and correlation analyses, nine MrMYB TFs were selected as candidates regulating flavonoid biosynthesis. By using dual-luciferase assays, MrMYB12 was shown to trans-activate the promoter, and MrMYB39 and MrMYB58a trans-activated the promoter. In addition, overexpression of 35S:MrMYB12 caused a significant increase in flavonol contents and induced the expression of , , and in transgenic tobacco leaves and flowers and significantly reduced anthocyanin accumulation, resulting in pale-pink or pure white flowers. This indicates that MrMYB12 redirected the flux away from anthocyanin biosynthesis resulting in higher flavonol content. The present study provides valuable information for understanding the classification, gene and motif structure, evolution and predicted functions of the gene family and identifies MYBs regulating different aspects of flavonoid biosynthesis in Chinese bayberry.
杨梅是杨梅科中经济价值最高的果树,是天然黄酮类化合物的丰富来源。最近,杨梅基因组已被测序,这为从全基因组角度研究基因的组织和进化特征提供了机会。在本研究中,我们对杨梅中的基因进行了全基因组分析,鉴定出174个MrMYB转录因子(TFs),包括122个R2R3-MYBs、43个1R-MYBs、2个3R-MYBs、1个4R-MYB和6个非典型MYBs。共线性分析表明,同线和串联重复都有助于该基因家族的扩展。转录水平分析揭示了不同基因的独特表达模式,以及那些可能在叶片和花发育中起重要作用的基因。通过系统发育分析和相关性分析,选择了9个MrMYB TFs作为调控类黄酮生物合成的候选基因。通过双荧光素酶测定,MrMYB12被证明可反式激活启动子,MrMYB39和MrMYB58a可反式激活启动子。此外,35S:MrMYB12的过表达导致黄酮醇含量显著增加,并诱导转基因烟草叶片和花中、和的表达,同时显著降低花青素积累,导致花朵呈浅粉色或纯白色。这表明MrMYB12将通量从花青素生物合成中转移,从而导致更高的黄酮醇含量。本研究为理解该基因家族的分类、基因和基序结构、进化及预测功能提供了有价值的信息,并鉴定了调控杨梅类黄酮生物合成不同方面的MYBs。