Yonekura-Sakakibara Keiko, Tohge Takayuki, Niida Rie, Saito Kazuki
RIKEN Plant Science Center, Yokohama 230-0045, Japan.
J Biol Chem. 2007 May 18;282(20):14932-41. doi: 10.1074/jbc.M611498200. Epub 2007 Feb 21.
Glycosylation plays a major role in the remarkable chemical diversity of flavonoids in plants including Arabidopsis thaliana. The wide diversity encoded by the large family-1 glycosyltransferase (UGT) gene family makes it difficult to determine the biochemical function of each gene solely from its primary sequence. Here we used transcriptome coexpression analysis combined with a reverse genetics approach to identify a gene that is prominent in determining the flavonoid composition of Arabidopsis. Using transcriptome coexpression analysis accessible on the ATTED-II public data base, the expression pattern of a UGT gene, UGT89C1, was found to be highly correlated with known flavonoid biosynthetic genes. No C-7 rhamnosylated flavonols were detected in either of two T-DNA ugt89c1 mutants. This specific metabolite deficiency in the mutants was complemented by stable transformation with the genomic fragment containing intact UGT89C1. Glutathione S-transferasefused recombinant UGT89C1 protein converted kaempferol 3-O-glucoside to kaempferol 3-O-glucoside-7-O-rhamnoside and recognized 3-O-glycosylated flavonols and UDP-rhamnose as substrates, but not flavonol aglycones, 3-O-glycosylated anthocyanins or other UDP-sugars. These results show that UGT89C1 is a flavonol 7-O-rhamnosyltransferase. The abundance of UGT89C1 transcripts in floral buds was consistent with the flavonoid accumulation of C-7 rhamnosylated flavonols in Arabidopsis organs. Our present study demonstrates that the integration of transcriptome coexpression analysis with a reverse genetic approach is a versatile tool for understanding a multigene family of a metabolic pathway in Arabidopsis.
糖基化在包括拟南芥在内的植物类黄酮显著的化学多样性中起着重要作用。由大家族1糖基转移酶(UGT)基因家族编码的广泛多样性使得仅从其一级序列确定每个基因的生化功能变得困难。在这里,我们使用转录组共表达分析结合反向遗传学方法来鉴定一个在决定拟南芥类黄酮组成方面突出的基因。利用ATTED-II公共数据库中可获取的转录组共表达分析,发现一个UGT基因UGT89C1的表达模式与已知的类黄酮生物合成基因高度相关。在两个T-DNA ugt89c1突变体中均未检测到C-7鼠李糖基化黄酮醇。用含有完整UGT89C1的基因组片段进行稳定转化,弥补了突变体中这种特定代谢物的缺乏。谷胱甘肽S-转移酶融合的重组UGT89C1蛋白将山奈酚3-O-葡萄糖苷转化为山奈酚3-O-葡萄糖苷-7-O-鼠李糖苷,并识别3-O-糖基化黄酮醇和UDP-鼠李糖作为底物,但不识别黄酮醇苷元、3-O-糖基化花青素或其他UDP-糖。这些结果表明UGT89C1是一种黄酮醇7-O-鼠李糖基转移酶。UGT89C1转录本在花芽中的丰度与拟南芥器官中C-7鼠李糖基化黄酮醇的类黄酮积累一致。我们目前的研究表明,转录组共表达分析与反向遗传学方法的整合是理解拟南芥代谢途径多基因家族的一种通用工具。