Li Jie, Xue Lexun, Yan Hongxia, Wang Lili, Liu Lingling, Lu Yumin, Xie Hua
Laboratory for Cell Biology, The First Affiliated Hospital, Zhengzhou University, Henan 450052, PR China.
Gene. 2007 Nov 15;403(1-2):132-42. doi: 10.1016/j.gene.2007.08.001. Epub 2007 Aug 19.
The control of promoter activity by nitrogen source has recently emerged as an intriguing system for regulated expression of the heterologous genes. The purpose of this work was to investigate whether heterologous gene expression in transgenic Dunaliella salina would be controlled by an inducible promoter. Here we identify that the nitrate reductase (NR) transcripts of D. salina are induced by nitrate but repressed by ammonium. The bar gene integrated into the genome of D. salina is transcribed by a promoter of the NR gene from D. salina and the bar transcripts are induced by nitrate but repressed by ammonium. PPT-resistance of transformants disappears when they are transferred from nitrate-containing medium to ammonium-containing medium. The findings of this study demonstrate that the promoter of the D. salina NR gene can be used to control expression of the heterologous genes in transgenic D. salina.
氮源对启动子活性的控制最近已成为一种用于调控异源基因表达的有趣系统。这项工作的目的是研究转基因盐生杜氏藻中异源基因的表达是否受诱导型启动子的控制。在此我们发现,盐生杜氏藻的硝酸还原酶(NR)转录本受硝酸盐诱导,但受铵抑制。整合到盐生杜氏藻基因组中的bar基因由盐生杜氏藻NR基因的启动子转录,bar转录本受硝酸盐诱导,但受铵抑制。当转化体从含硝酸盐的培养基转移到含铵的培养基时,其对PPT的抗性消失。本研究结果表明,盐生杜氏藻NR基因的启动子可用于控制转基因盐生杜氏藻中异源基因的表达。