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首页> 外文期刊>酒類総合研究所報告 >Functional characterization of a new grapevine MYB transcription factor and regulation of proanthocyanidin biosynthesis in grapes
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Functional characterization of a new grapevine MYB transcription factor and regulation of proanthocyanidin biosynthesis in grapes

机译:新的葡萄MYB转录因子的功能表征和原花青素在葡萄中的生物合成调控

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A new regulator of proanthocyanidin (PA) biosynthesis in grapes was found by screening genes coordinately expressed with PA accumulation under different light conditions using a substantially improved method of serial analysis of gene expression (SuperSAGE). This R2R3-MYB transcription factor, VvMYBPAR, shows high protein sequence similarity with PA biosynthesis-regulating plant MYBs, such as VvMYBPA2 and TRANSPARENT TESTA2. Its transcript levels were relatively high in the skins of young berries, whereas the levels were higher in the seeds and at a maximum around veraison. In addition to its response to modified light conditions, the gene responded to abscisic acid application in the skins of cultured berries. Among the PA-specific branch genes, this transcript profile was not correlated with that of VvANR and VvLAR1 but was closely related to that of VvLAR2, suggesting different regulation of PA-specific branch genes from that of a known PA regulator, VvMYBPA2. The PA-specific regulation of VvMYBPAR was confirmed by VvMYBPAR constitutive expression in Arabidopsis in which the transgene specifically induced PA biosynthetic genes and resulted in PA accumulation in plants grown on sucrose-supplemented media to induce anthocyanin synthesis. A transient reporter assay using grapevine cells showed that VvMYBPAR activated the promoters on PA-specific branch genes and candidate genes associated with modification and transport of monomeric PA precursors, as well as the promoters of VvCHS3 and VvF3'5'Hd in the common flavonoid pathway, but not that of VvUFGT on the anthocyanin-specific branch. This new factor suggests the polygenic regulation of PA biosynthesis in grapes by closely related MYB transcription factors.
机译:通过使用显着改进的基因表达序列分析方法(SuperSAGE),筛选了在不同光照条件下与PA积累协调表达的基因,从而发现了葡萄中原花青素(PA)生物合成的新调节剂。此R2R3-MYB转录因子VvMYBPAR与调节PA生物合成的植物MYB(例如VvMYBPA2和TRANSPARENT TESTA2)显示出高度的蛋白质序列相似性。在幼果的果皮中,其转录本水平相对较高,而在种子中则较高,并且在种子周围最高。除了对改变的光照条件有反应外,该基因还对脱落酸在培养后的浆果皮中的生长产生了响应。在PA特异性分支基因中,该转录本谱与VvANR​​和VvLAR1的转录谱无关,但与VvLAR2密切相关,这表明与已知PA调节剂VvMYBPA2的PA特异性分支基因调控不同。通过在拟南芥中的VvMYBPAR组成型表达证实了VvMYBPAR的PA特异性调节,其中转基因特异性诱导PA生物合成基因,并导致在蔗糖补充培养基上生长的植物中PA积累,从而诱导花色苷合成。使用葡萄细胞的瞬时报告基因分析表明,VvMYBPAR激活了PA特异性分支基因和候选基因上的启动子,这些基因与单体PA前体的修饰和运输有关,以及VvCHS3和VvF3'5'Hd在常见类黄酮途径中的启动子,而不是花青素特异性分支上的VvUFGT。这个新因子表明,密切相关的MYB转录因子对葡萄中PA生物合成的多基因调控。

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