Xiong Bo, Li Yisong, Yao Junfei, Wang Jialu, Han Linlyu, Ma Qingqing, Deng Taimei, Liao Ling, Deng Lijun, Sun Guochao, Zhang Mingfei, Wan Xun, He Siya, He Jiaxian, Wang Zhihui
College of Horticulture, Sichuan Agricultural University, Chengdu, 611130, China.
BMC Plant Biol. 2025 Mar 27;25(1):391. doi: 10.1186/s12870-025-06414-z.
The 'Yinhongli' cultivar of Chinese plum (Prunus salicina Lindl.) is characterized by a distinctive bicolored peel phenotype, in which anthocyanins serve as crucial determinants of both its visual characteristics and nutritional quality. However, the molecular mechanism of underlying light-dependent anthocyanin biosynthesis of plum, especially its regulatory network and pathway, need to be further studied and explored.
Comprehensive physiological analyses demonstrated distinct pigmentation patterns, revealing that dark-treated (YD) plum peels retained green coloration, whereas light-exposed (YL) and bag-removed samples (YDL) exhibited red pigmentation. Utilizing an integrated approach combining metabolomic and transcriptomic analyses, we identified 266 differentially accumulated flavonoids (DAFs), among which seven anthocyanin metabolites were established as principal determinants of peel coloration. Transcriptomic profiling revealed 6,900 differentially expressed genes (DEGs) between YD and YL, demonstrating significant correlations between the phenylpropanoid and flavonoid biosynthetic pathways. Through Weighted Gene Co-expression Network Analysis (WGCNA) and correlation heatmap analysis, we identified crucial regulatory networks encompassing five structural genes (PAL, 4CL, F3'H, CHI, and UFGT) and 15 candidate regulatory genes, including six light signal transduction factor genes (UVR8, COP1, PHYBs, PIF3, and HY5) and nine transcription factor genes (MYB1, MYB20, MYB73, MYB111, LHY, DRE2B, ERF5, bHLH35, and NAC87). Subsequent RT-qPCR validation demonstrated significant light-mediated up-regulation of key structural genes (PAL, F3H, CHI, 4CL, and UFGT) involved in anthocyanin biosynthesis along with positive regulatory factors (DRE2B and NAC87). Conversely, a cohort of negative regulators, including HY5, MYB1, MYB20, MYB73, MYB111, LHY, ERF5, and bHLH35, showed marked down-regulation in response to light exposure, suggesting their potential repressive roles in the light-dependent anthocyanin biosynthesis pathway.
This investigation provides comprehensive insights into the molecular mechanisms of anthocyanin biosynthesis in light-dependent anthocyanin biosynthesis in 'Yinhongli' plum, identifying critical structural genes and potential regulatory TFs. The findings offer substantial contributions to the understanding of anthocyanin regulation in fruit crops and provide a valuable foundation for molecular breeding initiatives aimed at enhancing quality traits in plum cultivars.
中国李(Prunus salicina Lindl.)的‘银红李’品种具有独特的双色果皮表型,其中花青素是其视觉特征和营养品质的关键决定因素。然而,李果实光依赖型花青素生物合成的分子机制,尤其是其调控网络和途径,仍需进一步研究和探索。
综合生理分析表明了明显的色素沉着模式,揭示了黑暗处理(YD)的李果皮保持绿色,而光照处理(YL)和去袋处理的样品(YDL)呈现红色色素沉着。利用代谢组学和转录组学分析相结合的综合方法,我们鉴定出266种差异积累的黄酮类化合物(DAFs),其中七种花青素代谢物被确定为果皮着色的主要决定因素。转录组分析揭示了YD和YL之间有6900个差异表达基因(DEGs),表明苯丙烷类和黄酮类生物合成途径之间存在显著相关性。通过加权基因共表达网络分析(WGCNA)和相关热图分析,我们确定了关键调控网络,包括五个结构基因(PAL、4CL、F'3H、CHI和UFGT)和15个候选调控基因,其中包括六个光信号转导因子基因(UVR8、COP1、PHYBs、PIF3和HY5)和九个转录因子基因(MYB1、MYB20、MYB73、MYB111、LHY、DRE2B、ERF5、bHLH35和NAC87)。随后的RT-qPCR验证表明,参与花青素生物合成的关键结构基因(PAL、F3H、CHI、4CL和UFGT)以及正向调控因子(DRE2B和NAC87)在光照下显著上调。相反,包括HY5、MYB1、MYB20、MYB73、MYB111、LHY、ERF5和bHLH35在内的一组负调控因子在光照下显著下调,表明它们在光依赖型花青素生物合成途径中可能发挥抑制作用。
本研究为‘银红李’果实光依赖型花青素生物合成的分子机制提供了全面的见解,鉴定出关键结构基因和潜在调控转录因子。这些发现为理解果树作物中花青素的调控提供了重要贡献,并为旨在改善李品种品质性状的分子育种计划提供了有价值的基础。