Agrigenetics Advanced Sciences Corporation, 5649 Buckeye Road, 53711, Madison, WI, USA.
Plant Cell Rep. 1990 Jul;9(3):129-32. doi: 10.1007/BF00232087.
We describe a method for direct analysis of RNA transcribed from DNA introduced into carrot cells by electroporation. Octopine synthase RNA transcribed from the plasmid p35SOcs was detected in total and poly A(+) RNA on Northern blots and in RNA protection assays. The highest level of octopine synthase transcript was detected at approximately 8 hrs post-electroporation, although RNA could still be detected after 48 hrs. This method allows detection of foreign gene expression in a plant system and bypasses the need for reporter genes.
我们描述了一种通过电穿孔将 DNA 导入胡萝卜细胞后直接分析 RNA 的方法。在 Northern 印迹和 RNA 保护分析中,检测到来自质粒 p35SOcs 的 octopine 合酶 RNA 在总 RNA 和 poly A(+) RNA 中的转录。尽管在 48 小时后仍能检测到 RNA,但在外源基因表达检测到最高水平的 octopine 合酶转录大约在电穿孔后 8 小时。该方法允许在植物系统中检测外源基因表达,并且绕过了对报告基因的需求。