College of Horticulture, Northwest A&F University, Yangling, Shaanxi, 712100, China.
Plant Mol Biol. 2019 Jul;100(4-5):451-465. doi: 10.1007/s11103-019-00870-6. Epub 2019 May 11.
AcGST1, an anthocyanin-related GST, may functions as a carrier to transport anthocyanins from ER to tonoplast in kiwifruit. It was positively regulated by AcMYBF110 through directly binding to its promoter. Anthocyanins are synthesized in the cytoplasmic surface of the endoplasmic reticulum but accumulate predominantly in the vacuole. Previous studies in model and ornamental plants have suggested that a member of the glutathione S-transferase (GST) gene family is involved in sequestration of anthocyanins into the vacuole. However, little is known about anthocyanin-related GST protein in kiwifruit. Here, four putative AcGSTs were identified from the genome of the red-fleshed Actinidia chinensis cv 'Hongyang'. Expression analyses reveal only the expression of AcGST1 was highly consistent with anthocyanin accumulation. Molecular complementation of Arabidopsis tt19 demonstrates AcGST1 can complement the anthocyanin-less phenotype of tt19. Transient expression in Actinidia arguta fruits further confirms that AcGST1 is functional in anthocyanin accumulation in kiwifruit. In vitro assays show the recombinant AcGST1 increases the water solubility of cyanidin-3-O-galactoside (C3Gal) and cyanidin-3-O-xylo-galactoside (C3XG). We further show that AcGST1 protein is localized not only in the ER but also on the tonoplast, indicating AcGST1 (like AtTT19) may functions as a carrier protein to transport anthocyanins to the tonoplast in kiwifruit. Moreover, the promoter of AcGST1 can be activated by AcMYBF110, based on results from transient dual-luciferase assays and yeast one-hybrid assays. EMSAs show that AcMYBF110 binds directly to CAGTTG and CCGTTG motifs in the AcGST1 promoter. These results indicate that AcMYBF110 plays an important role in transcriptional regulation of AcGST1 and, therefore, in controlling accumulation of anthocyanins in kiwifruit.
AcGST1,一种与花青素相关的 GST,可能作为载体将花青素从内质网运输到猕猴桃的液泡中。它通过直接结合其启动子被 AcMYBF110 正向调控。花青素在细胞质内质网的内表面合成,但主要积累在液泡中。先前在模式植物和观赏植物中的研究表明,谷胱甘肽 S-转移酶(GST)基因家族的一个成员参与将花青素隔离到液泡中。然而,关于猕猴桃中与花青素相关的 GST 蛋白知之甚少。在这里,从红肉猕猴桃基因组中鉴定出四个推定的 AcGSTs。表达分析表明,只有 AcGST1 的表达与花青素积累高度一致。拟南芥 tt19 的分子互补表明 AcGST1 可以互补 tt19 的花青素缺失表型。在软枣猕猴桃果实中的瞬时表达进一步证实 AcGST1 在猕猴桃花青素积累中具有功能。体外实验表明,重组 AcGST1 增加了矢车菊素-3-O-半乳糖苷(C3Gal)和矢车菊素-3-O-木糖半乳糖苷(C3XG)的水溶性。我们进一步表明,AcGST1 蛋白不仅定位于内质网,也定位于液泡膜上,表明 AcGST1(像 AtTT19)可能作为载体蛋白将花青素运输到猕猴桃的液泡膜中。此外,基于瞬时双荧光素酶测定和酵母单杂交测定的结果,AcGST1 的启动子可以被 AcMYBF110 激活。EMSA 表明 AcMYBF110 直接结合 AcGST1 启动子中的 CAGTTG 和 CCGTTG 基序。这些结果表明 AcMYBF110 在 AcGST1 的转录调控中起重要作用,因此在控制猕猴桃中花青素的积累中起重要作用。