Rinaldo Amy R, Cavallini Erika, Jia Yong, Moss Sarah M A, McDavid Debra A J, Hooper Lauren C, Robinson Simon P, Tornielli Giovanni B, Zenoni Sara, Ford Christopher M, Boss Paul K, Walker Amanda R
Commonwealth Scientific and Industrial Research Organization-Agriculture, Wine Innovation West, Hartley Grove, South Australia 5064, Australia (A.R.R., S.M.A.M., D.A.J.M., L.C.H., S.P.R., P.K.B., A.R.W.);School of Agriculture, Food, and Wine, University of Adelaide, Adelaide, South Australia 5005, Australia (A.R.R., Y.J., S.M.A.M., C.M.F.); andDepartment of Biotechnology, University of Verona, 37134 Verona, Italy (E.C., G.B.T., S.Z.).
Commonwealth Scientific and Industrial Research Organization-Agriculture, Wine Innovation West, Hartley Grove, South Australia 5064, Australia (A.R.R., S.M.A.M., D.A.J.M., L.C.H., S.P.R., P.K.B., A.R.W.);School of Agriculture, Food, and Wine, University of Adelaide, Adelaide, South Australia 5005, Australia (A.R.R., Y.J., S.M.A.M., C.M.F.); andDepartment of Biotechnology, University of Verona, 37134 Verona, Italy (E.C., G.B.T., S.Z.)
Plant Physiol. 2015 Nov;169(3):1897-916. doi: 10.1104/pp.15.01255. Epub 2015 Sep 22.
Anthocyanins are flavonoid compounds responsible for red/purple colors in the leaves, fruit, and flowers of many plant species. They are produced through a multistep pathway that is controlled by MYB transcription factors. VvMYBA1 and VvMYBA2 activate anthocyanin biosynthesis in grapevine (Vitis vinifera) and are nonfunctional in white grapevine cultivars. In this study, transgenic grapevines with altered VvMYBA gene expression were developed, and transcript analysis was carried out on berries using a microarray technique. The results showed that VvMYBA is a positive regulator of the later stages of anthocyanin synthesis, modification, and transport in cv Shiraz. One up-regulated gene, ANTHOCYANIN 3-O-GLUCOSIDE-6″-O-ACYLTRANSFERASE (Vv3AT), encodes a BAHD acyltransferase protein (named after the first letter of the first four characterized proteins: BEAT [for acetyl CoA:benzylalcohol acetyltransferase], AHCT [for anthocyanin O-hydroxycinnamoyltransferase], HCBT [for anthranilate N-hydroxycinnamoyl/benzoyltransferase], and DAT [for deacetylvindoline 4-O-acetyltransferase]), belonging to a clade separate from most anthocyanin acyltransferases. Functional studies (in planta and in vitro) show that Vv3AT has a broad anthocyanin substrate specificity and can also utilize both aliphatic and aromatic acyl donors, a novel activity for this enzyme family found in nature. In cv Pinot Noir, a red-berried grapevine mutant lacking acylated anthocyanins, Vv3AT contains a nonsense mutation encoding a truncated protein that lacks two motifs required for BAHD protein activity. Promoter activation assays confirm that Vv3AT transcription is activated by VvMYBA1, which adds to the current understanding of the regulation of the BAHD gene family. The flexibility of Vv3AT to use both classes of acyl donors will be useful in the engineering of anthocyanins in planta or in vitro.
花青素是一类黄酮类化合物,赋予许多植物物种的叶子、果实和花朵红色或紫色。它们通过一个由MYB转录因子控制的多步骤途径产生。VvMYBA1和VvMYBA2激活葡萄(Vitis vinifera)中的花青素生物合成,而在白葡萄品种中无功能。在本研究中,构建了VvMYBA基因表达改变的转基因葡萄,并使用微阵列技术对浆果进行转录分析。结果表明,VvMYBA是设拉子葡萄品种花青素合成、修饰和转运后期的正调控因子。一个上调基因,花青素3-O-葡萄糖苷-6″-O-酰基转移酶(Vv3AT),编码一种BAHD酰基转移酶蛋白(以最初四个被鉴定蛋白的首字母命名:BEAT [乙酰辅酶A:苄醇乙酰转移酶]、AHCT [花青素O-羟基肉桂酰转移酶]、HCBT [邻氨基苯甲酸N-羟基肉桂酰/苯甲酰转移酶]和DAT [去乙酰文朵灵4-O-乙酰转移酶]),属于与大多数花青素酰基转移酶不同的一个进化枝。功能研究(在植物体内和体外)表明,Vv3AT具有广泛的花青素底物特异性,并且还可以利用脂肪族和芳香族酰基供体,这是该酶家族在自然界中发现的一种新活性。在黑皮诺葡萄品种中,一个缺乏酰化花青素的红浆果葡萄突变体,Vv3AT包含一个无义突变,编码一个截短的蛋白,该蛋白缺乏BAHD蛋白活性所需的两个基序。启动子激活分析证实Vv3AT转录由VvMYBA1激活,这增加了对BAHD基因家族调控的当前理解。Vv3AT使用两类酰基供体的灵活性将有助于在植物体内或体外对花青素进行工程改造。