Halweg Christopher, Thompson William F, Spiker Steven
Department of Genetics, North Carolina State University, Raleigh, North Carolina 27695-7614, USA.
Plant Cell. 2005 Feb;17(2):418-29. doi: 10.1105/tpc.104.028100. Epub 2005 Jan 19.
Many studies in both plant and animal systems have shown that matrix attachment regions (MARs) can increase expression of transgenes in whole organisms or cells in culture. Because histochemical assays often indicate variegated transgene expression, a question arises: Do MARs increase transgene expression by increasing the percentage of cells expressing the transgene (likelihood), by increasing the level of expression in expressing cells (magnitude), or both? To address this question, we used flow cytometry to measure green fluorescent protein (GFP) expression in individual tobacco (Nicotiana tabacum) cells from lines transformed by Agrobacterium tumefaciens. We conclude that MAR-mediated overall increases in transgene expression involve both likelihood and magnitude. On average, cell lines transformed with the Rb7 MAR-containing vector expressed GFP at levels 2.0- to 3.7-fold higher than controls. MAR lines had fewer nonexpressing cells than control lines (10% versus 45%), and the magnitude of GFP expression in expressing cells was greater in MAR lines by 1.9- to 2.9-fold. We also show that flow cytometry measurements on cells from isogenic lines are consistent with those from populations of independently transformed cell lines. By obviating the need to establish isogenic lines, this use of flow cytometry could greatly simplify the evaluation of MARs or other sequence elements that affect transgene expression.
在植物和动物系统中的许多研究表明,基质附着区域(MARs)能够提高转基因在整个生物体或培养细胞中的表达。由于组织化学分析常常显示转基因表达呈斑驳状,因此出现了一个问题:MARs是通过提高表达转基因的细胞百分比(可能性)、提高表达细胞中的表达水平(幅度),还是两者兼具来提高转基因表达?为了解决这个问题,我们使用流式细胞术来测量来自经根癌农杆菌转化的烟草(Nicotiana tabacum)品系的单个细胞中绿色荧光蛋白(GFP)的表达。我们得出结论,MAR介导的转基因表达总体增加涉及可能性和幅度两个方面。平均而言,用含Rb7 MAR的载体转化的细胞系表达GFP的水平比对照高2.0至3.7倍。MAR品系中不表达的细胞比对照品系少(10%对45%),并且MAR品系中表达细胞中GFP的表达幅度比对照高1.9至2.9倍。我们还表明,对同基因系细胞的流式细胞术测量结果与来自独立转化细胞系群体的测量结果一致。通过无需建立同基因系,这种流式细胞术的应用可以极大地简化对MARs或其他影响转基因表达的序列元件的评估。