Koshino-Kimura Yoshihiro, Takenaka Kosuke, Domoto Fumiya, Aoyama Yasuhiro, Sera Takashi
Department of Synthetic Chemistry and Biological Chemistry, Graduate School of Engineering, Kyoto University, Kyotodaigaku-Katsura, Nishikyo-ku, Kyoto 615-8510, Japan.
Nucleic Acids Symp Ser (Oxf). 2008(52):189-90. doi: 10.1093/nass/nrn096.
Previously, we designed an artificial zinc-finger protein (AZP) for blocking a replication protein (Rep) of beet severe curly top virus (BSCTV) from binding to its replication origin and demonstrated that transgenic Arabidopsis plants expressing the AZP are completely resistant to the virus infection. Here we applied the AZP technology to tomato yellow leaf curl virus (TYLCV) infective to an important agricultural crop, tomato. We designed and constructed an AZP binding to the direct repeat to block the TYLCV Rep binding. In gel shift assays, we confirmed that the designed AZP has a higher affinity to the replication origin than that of Rep and that the AZP effectively inhibited the Rep binding to its replication origin in vitro. The AZP gene was then introduced into a plant genome with the help of Agrobacterium tumefaciens to generate the transgenic plants. We will discuss properties of the AZP-transgenic plants against TYLCV infection.
此前,我们设计了一种人工锌指蛋白(AZP),用于阻止甜菜严重曲顶病毒(BSCTV)的复制蛋白(Rep)与其复制起点结合,并证明表达该AZP的转基因拟南芥植株对病毒感染具有完全抗性。在此,我们将AZP技术应用于对重要农作物番茄具有感染性的番茄黄化曲叶病毒(TYLCV)。我们设计并构建了一种与直接重复序列结合的AZP,以阻止TYLCV Rep的结合。在凝胶迁移实验中,我们证实所设计的AZP对复制起点的亲和力高于Rep,并且该AZP在体外有效抑制了Rep与其复制起点的结合。然后借助根癌农杆菌将AZP基因导入植物基因组以产生转基因植株。我们将讨论AZP转基因植株对TYLCV感染的抗性特性。