Nagao Nobuyoshi, Suzuki Hiromichi, Numano Rika, Umekage So, Kikuchi Yo
Department of Environmental and Life Sciences, Toyohashi University of Technology.
J Gen Appl Microbiol. 2014;60(6):222-6. doi: 10.2323/jgam.60.222.
Previously, we proposed a new method for production of RNA aptamers using the marine bacterium Rhodovulum sulfidophilum. A streptavidin RNA aptamer (an RNA which binds to streptavidin) was extracellularly produced by this bacterium containing engineered plasmid. The aptamer had full biological function. As a next step we attempted to produce another functional RNA, short hairpin RNAs (shRNAs) using this bacterial system. We have designed two types of shRNAs targeted to the luciferase gene. Here we report that shRNAs are successfully produced extracellularly by this system. Even if the shRNA has a long stem-loop structure which is thought to interfere with transcription in bacterial cells, the yield of the shRNA is almost the same as that of the streptavidin RNA aptamer. During the course of these experiments, we also found a new type of RNA processing for the double-stranded region of the shRNA.
此前,我们提出了一种利用嗜硫小红卵菌生产RNA适体的新方法。一种链霉亲和素RNA适体(一种与链霉亲和素结合的RNA)由含有工程质粒的这种细菌在细胞外产生。该适体具有完整的生物学功能。下一步,我们尝试利用这个细菌系统生产另一种功能性RNA,即短发夹RNA(shRNA)。我们设计了两种靶向荧光素酶基因的shRNA。在此我们报告,该系统成功地在细胞外产生了shRNA。即使shRNA具有被认为会干扰细菌细胞转录的长茎环结构,其产量与链霉亲和素RNA适体的产量几乎相同。在这些实验过程中,我们还发现了一种针对shRNA双链区域的新型RNA加工方式。