Enayati Somayeh, Azizi Mohammad, Aminollahi Elahe, Ranjvar Shahrivar Mona, Khalaj Vahid
Medical Biotechnology Department, Biotechnology Research Center, Pasteur Institute of Iran, Pasteur Ave, 1316943551 Tehran, Iran.
Medical Biotechnology Department, Biotechnology Research Center, Pasteur Institute of Iran, Pasteur Ave, 1316943551 Tehran, Iran
FEMS Microbiol Lett. 2016 Mar;363(5):fnw029. doi: 10.1093/femsle/fnw029. Epub 2016 Feb 5.
An RNAi system based on T7 RNA polymerase (TRNAP) was designed and examined in Aspergillus fumigatus. This system consists of two elements; an inducible T7RNAP expressing cassette and an AMA1-based episomal RNAi plasmid. These constructs were transformed into the A. fumigatus protoplasts and the efficiency of this system was tested in downregulation of alb1 gene. Upon the induction of T7RNAP expression, the recombinant T7RNAP was able to recognize T7 promoters, which were located on the episomal plasmid and in opposite direction. As a result, the bidirectional transcription of alb1 fragment led to the silencing of the target gene. However, our results demonstrated that this silencing system is unstable and may not be applicable in preparation of RNAi libraries.
设计了一种基于T7 RNA聚合酶(TRNAP)的RNA干扰系统,并在烟曲霉中进行了检测。该系统由两个元件组成;一个可诱导的T7RNAP表达盒和一个基于AMA1的附加型RNA干扰质粒。将这些构建体转化到烟曲霉原生质体中,并在下调alb1基因的过程中测试了该系统的效率。在诱导T7RNAP表达后,重组T7RNAP能够识别位于附加型质粒上且方向相反的T7启动子。结果,alb1片段的双向转录导致了靶基因的沉默。然而,我们的结果表明,这种沉默系统不稳定,可能不适用于制备RNA干扰文库。