Triccas James A, Britton Warwick J, Gicquel Brigitte
Centenary Institute of Cancer Medicine and Cell Biology, Locked Bag No. 6, Newtown, NSW, 2042, Australia2.
Unité de Génétique Mycobactérienne, Institut Pasteur, 25 rue du Dr Roux, 75724 Paris Cedex 15, France1.
Microbiology (Reading). 2001 May;147(Pt 5):1253-1258. doi: 10.1099/00221287-147-5-1253.
The natural fluorescence of the Aequoria victoria green fluorescent protein was exploited to isolate strong expression signals of Mycobacterium tuberculosis. Mycobacterium bovis bacille Calmette-Guérin harbouring M. tuberculosis fragments driving high levels of gfp expression were isolated by fluorescence-activated cell sorting (FACS). DNA sequencing and subsequent comparison with the M. tuberculosis genome sequence revealed that a total of nine postulated promoters had been identified. The majority of the promoters displayed activity that was greater than or equal to the Mycobacterium fortuitum beta-lactamase promoter, one of the strongest mycobacterial promoters characterized to date. Two of the promoters corresponded to proteins predicted to be involved in calcium and magnesium utilization, the importance of such functions for cell physiology suggesting why these two genes are controlled by strong transcription signals. The seven other promoters corresponded to genes encoding proteins of unknown function. Promoter activity was maintained after prolonged incubation within macrophages, implying that these promoters could be used to drive sustained foreign gene expression in vivo. The strength of these expression signals identified could be employed for the overexpression of foreign genes in mycobacteria to aid protein purification and vaccine vector development. Furthermore, this study demonstrated that FACS provides a sensitive and efficient technique to measure and select strong mycobacterial expression signals.
利用维多利亚多管水母绿色荧光蛋白的天然荧光来分离结核分枝杆菌的强表达信号。通过荧光激活细胞分选(FACS)分离出携带驱动高水平绿色荧光蛋白(gfp)表达的结核分枝杆菌片段的卡介苗。DNA测序以及随后与结核分枝杆菌基因组序列的比较显示,总共鉴定出9个假定的启动子。大多数启动子表现出的活性大于或等于偶然分枝杆菌β-内酰胺酶启动子,后者是迄今为止所鉴定的最强的分枝杆菌启动子之一。其中两个启动子对应于预测参与钙和镁利用的蛋白质,此类功能对细胞生理学的重要性提示了这两个基因受强转录信号控制的原因。其他七个启动子对应于编码功能未知蛋白质的基因。在巨噬细胞内长时间孵育后,启动子活性得以维持,这意味着这些启动子可用于驱动体内持续的外源基因表达。所鉴定出的这些表达信号的强度可用于分枝杆菌中外源基因的过表达,以辅助蛋白质纯化和疫苗载体开发。此外,本研究表明FACS提供了一种灵敏且高效的技术来测量和选择强分枝杆菌表达信号。