Liu Xinya, Chen Beibei, Luo Ling, Zhong Qi, Teo Chee How, Huang Shengjia
Horticulture Research Institute, Sichuan Academy of Agricultural Sciences, Chengdu 610023, China.
Key Laboratory of Horticultural Crops Biology and Germplasm Enhancement in Southwest, Ministry of Agriculture and Rural Affairs, Chengdu 611130, China.
Plants (Basel). 2025 Jun 24;14(13):1936. doi: 10.3390/plants14131936.
Flavonoid synthases (FNSs) are key enzymes catalyzing the conversion of flavanones to flavonoids, yet their functions in citrus remain functionally uncharacterized. In this study, we identified three FNSII genes in the citrus genome. Phylogenetic analysis revealed that citrus FNSII genes share the closest evolutionary distance with apple FNSII genes. Chromosomal localization demonstrated that the three FNSII genes are distributed across two out of nine chromosomes. Gene structure analysis indicated that the majority of motifs within these three FNSII genes are highly conserved. We cloned a gene called from citrus. Transient overexpression of in citrus leaves significantly increased flavonoid content, while simultaneous virus-induced silencing of led to synchronously and significantly reduced gene expression levels and flavonoid content in citrus seedlings. Through the -mediated genetic transformation system, overexpression of was found to markedly enhance flavonoid accumulation in hairy roots, whereas knockout of resulted in a significant decrease in flavonoid content in hairy roots. Further experiments verified an interaction between CitFNSII-1 and the Chalcone isomerase-1 (CHI-1) protein. The results demonstrated that the flavonoid accumulation patterns of and are highly similar. In conclusion, this study advances the understanding of the flavonoid biosynthesis pathway in citrus and provides a theoretical foundation for molecular breeding strategies in citrus.
类黄酮合酶(FNSs)是催化黄烷酮转化为类黄酮的关键酶,但其在柑橘中的功能仍未得到功能性表征。在本研究中,我们在柑橘基因组中鉴定出三个FNSII基因。系统发育分析表明,柑橘FNSII基因与苹果FNSII基因的进化距离最近。染色体定位显示,这三个FNSII基因分布在九条染色体中的两条上。基因结构分析表明,这三个FNSII基因中的大多数基序高度保守。我们从柑橘中克隆了一个名为 的基因。 在柑橘叶片中的瞬时过表达显著增加了类黄酮含量,而同时对 进行病毒诱导沉默则导致柑橘幼苗中基因表达水平和类黄酮含量同步且显著降低。通过 -介导的遗传转化系统,发现 的过表达显著增强了毛状根中类黄酮的积累,而 的敲除导致毛状根中类黄酮含量显著降低。进一步的实验证实了CitFNSII-1与查尔酮异构酶-1(CHI-1)蛋白之间的相互作用。结果表明, 和 的类黄酮积累模式高度相似。总之,本研究推进了对柑橘类黄酮生物合成途径的理解,并为柑橘分子育种策略提供了理论基础。