Materna Stefan C, Marwan Wolfgang
Institut für BiologieIII, Albert-Ludwigs-Universität, Schänzlestrasse 1, 79104 Freiburg im Breisgau, Germany.
FEMS Microbiol Lett. 2005 Feb 1;243(1):29-35. doi: 10.1016/j.femsle.2004.11.035.
We have estimated the statistical distribution of the number of plasmids taken up by individual Jurkat lymphoma cells during electroporation in the presence of two plasmids, one encoding for yellow (EYFP) the other for cyan (ECFP) fluorescent protein. The plasmid concentration at which most of the cells take up only one plasmid or several molecules was determined by statistical analysis. We found that cells behaved slightly heterogeneous in plasmid uptake and describe how the homogeneity of a cell population can be quantified by Poisson statistics in order to identify experimental conditions that yield homogeneously transfection-competent cell populations. The experimental procedure worked out with Jurkat cells was applied to assay the effectiveness of antisense RNA in knocking down gene expression in Physarum polycephalum. Double transfection of flagellates with vectors encoding EYFP and antisense-EYFP revealed for the first time that gene expression can be suppressed by co-expression of antisense RNA in Physarum. Quantitative analysis revealed that one copy of antisense expressing gene per EYFP gene was sufficient to completely suppress formation of the EYFP protein in Physarum.
我们估计了在存在两种质粒(一种编码黄色荧光蛋白(EYFP),另一种编码青色荧光蛋白(ECFP))的情况下,单个Jurkat淋巴瘤细胞在电穿孔过程中摄取的质粒数量的统计分布。通过统计分析确定了大多数细胞仅摄取一个质粒或几个分子时的质粒浓度。我们发现细胞在质粒摄取方面表现出轻微的异质性,并描述了如何通过泊松统计来量化细胞群体的同质性,以确定产生均匀转染能力细胞群体的实验条件。用Jurkat细胞制定的实验程序被应用于测定反义RNA在多头绒泡菌中敲低基因表达的有效性。用编码EYFP和反义-EYFP的载体对鞭毛虫进行双重转染首次揭示,在多头绒泡菌中,反义RNA的共表达可以抑制基因表达。定量分析表明,每个EYFP基因一个反义表达基因拷贝足以完全抑制多头绒泡菌中EYFP蛋白的形成。