苋菜AmaDOPA5-GT基因启动子的克隆、蛋白亚细胞定位及表达分析
loning of AmaDOPA5-GT promoter, protein subcellular localization and gene expression analysis in Amaranth tricolor
对AmaDOPA5-GT基因进行了生物信息学和蛋白亚细胞定位分析,并利用染色体步移技术克隆了该基因的启动子。亚细胞定位结果表明,AmaDOPA5-GT定位于细胞膜。启动子分析结果表明AmaDOPA5-GT启动子中植物光响应元件多达8个,说明光对该基因的表达影响较大。色素含量测定及实时定量PCR结果显示:暗处理抑制苋菜苷的合成表达和AmaDOPA5-GT;黄光和绿光抑制苋菜苷合成但对AmaDOPA5-GT表达影响不大;红光显著抑制苋菜苷合成但却显著诱导AmaDOPA5-GT的表达;蓝光显著促进苋菜苷的合成和AmaDOPA5-GT表达。
In this study, the bioinformatics characteristics and protein subcellular localization of AmaDOPA5-GT in Amaranth xx were analyzed. Moreover, chromosome walking technique was applied to clone the gene's promoter. Protein subcellular location result showed that this protein was located in the cytomembrane. Interestingly, 8 light-responsive elements were identified in the promoter, suggesting that light may function in regulating the gene's expression. Amaranthine content and quantitative real time PCR result showed that: dark treatment suppressed both the betalain biosynthesis and gene expression level, red light suppressed betalain biosynthesis but induced the expression of this gene, yellow and green light showed no influence on expression of this gene but suppressed the betalain biosynthesis, blue light, however, induced both betalain biosynthesis and expression level of AmaDOPA5-GT.
程春振、赖钟雄、郑学立、谢礼洋、刘生财
分子生物学植物学生物化学
苋菜DOPA5-GT启动子光质甜菜红色素
maranthDOPA5-GTpromoterlight qualitybetalain biosynthesis
程春振,赖钟雄,郑学立,谢礼洋,刘生财.苋菜AmaDOPA5-GT基因启动子的克隆、蛋白亚细胞定位及表达分析[EB/OL].(2015-11-02)[2025-08-16].http://www.paper.edu.cn/releasepaper/content/201511-13.点此复制
评论