College of Landscape Architecture and Art, Northwest A&F University, Yangling, Xianyang 712100, China.
Int J Mol Sci. 2022 Aug 12;23(16):9051. doi: 10.3390/ijms23169051.
Anthocyanins belong to a group of flavonoids, which are the most important flower pigments. Clarifying the potential anthocyanins biosynthesis molecular mechanisms could facilitate artificial manipulation of flower pigmentation in plants. In this paper, we screened a differentially expressed gene, , from the transcriptome data of petals at different development stages and explored its role in anthocyanins biosynthesis. The transcriptome data and qRT-PCR analysis showed that the expression level of gradually decreased from the flower color fades. Tissue specific expression analysis showed was expressed in the petal, leaf, and fruit of , and was highly expressed in the scarlet petal. Overexpression of promoted anthocyanins accumulation and increased pigments in infected parts of 'Snowdrift' and 'Fuji' fruit peels. In contrast, when endogenous was silenced, the anthocyanins accumulation was inhibited and pigments decreased in the infected peels. The qRT-PCR analysis revealed that overexpression or silence of caused expression changes of a series of structural genes included in anthocyanins biosynthesis pathway. The yeast two-hybrid assays indicated that MhTCP4 did not interact with MhMYB10. Furthermore, the yeast one-hybrid assays indicated that MhTCP4 did not directly bind to the promoter of , but that of the anthocyanins biosynthesis genes, and . Dual luciferase assays further confirmed that MhTCP4 can strongly activate the promoters of and in tobacco. Overall, the results suggest that positively regulates anthocyanins biosynthesis by directly activated and in flowers.
花色素苷属于类黄酮的一种,是最重要的花色素。阐明花色素苷生物合成的分子机制,可以促进植物花色的人工调控。本文从不同发育阶段花瓣的转录组数据中筛选出一个差异表达基因 ,并探讨其在花色素苷生物合成中的作用。转录组数据和 qRT-PCR 分析表明, 基因的表达水平逐渐降低,花色逐渐褪色。组织特异性表达分析表明 基因在 叶片、果实中的表达,且在猩红花瓣中高表达。过表达 基因促进花色素苷积累,增加 果皮和 '富士'果皮感染部位的色素含量。相比之下,当内源 基因沉默时,花色素苷的积累受到抑制,感染部位的色素含量下降。qRT-PCR 分析显示, 基因的过表达或沉默导致花色素苷生物合成途径中一系列结构基因的表达发生变化。酵母双杂交实验表明 MhTCP4 与 MhMYB10 不相互作用。此外,酵母单杂交实验表明 MhTCP4 不能直接结合 基因的启动子,但可以结合花色素苷生物合成基因 和 的启动子。双荧光素酶报告基因实验进一步证实 MhTCP4 可以在烟草中强烈激活 和 基因的启动子。综上所述,研究结果表明 基因通过直接激活 和 基因在 花中正向调控花色素苷的生物合成。