Koo Ja Choon, Asurmendi Sebastian, Bick Jennifer, Woodford-Thomas Terry, Beachy Roger N
Donald Danforth Plant Science Center, 975 N. Warson Road, Saint Louis, MO 63132, USA.
Plant J. 2004 Feb;37(3):439-48. doi: 10.1046/j.1365-313x.2003.01869.x.
Constitutive expression of a gene encoding tobacco mosaic virus (TMV) coat protein (CP) in transgenic plants confers resistance to infection by TMV and related tobamoviruses. Here, we examined resistance to TMV by temporal and quantitative control of TMV Cg CP (CgCP) gene expression using a simple, methoxyfenozide-inducible system in Arabidopsis plants. By soil drenching with a commercial ecdysone agonist (Intrepid-2F/methoxyfenozide), most transgenic lines were induced from undetectable levels of gene expression to protein levels from 0.05 to 0.8% (w/w) of CgCP. This corresponds to up to four times the amount of CP produced by the constitutive cauliflower mosaic virus (CaMV) double 35S promoter. CgCP transcripts were induced by 700-fold, without changing the expression patterns of pathogenesis-related (PR) genes. The high level of accumulation of CgCP was sufficient to produce large amounts of virus-like particles that accumulate in large aggregates throughout the cells. In virus challenge assays, treatment with Intrepid-2F prior to TMV infection resulted in high levels of viral resistance, while no treatment or treatment with the inducer following infection did not confer resistance. This report demonstrates chemically controlled disease resistance and confirms the utility of the ecdysone agonist-inducible system under greenhouse conditions.
在转基因植物中组成型表达编码烟草花叶病毒(TMV)外壳蛋白(CP)的基因可使植物对TMV及相关烟草花叶病毒的感染产生抗性。在此,我们利用拟南芥中一个简单的甲氧虫酰肼诱导系统,通过对TMV Cg CP(CgCP)基因表达进行时间和定量控制,来检测对TMV的抗性。通过用商业蜕皮激素激动剂(Intrepid - 2F/甲氧虫酰肼)进行土壤浇灌,大多数转基因株系从不可检测的基因表达水平被诱导至CgCP蛋白水平达到0.05%至0.8%(w/w)。这相当于组成型花椰菜花叶病毒(CaMV)双35S启动子产生的CP量的四倍。CgCP转录本被诱导了700倍,而不改变病程相关(PR)基因的表达模式。CgCP的高水平积累足以产生大量在整个细胞中以大聚集体形式积累的病毒样颗粒。在病毒挑战试验中,在TMV感染前用Intrepid - 2F处理导致高水平的病毒抗性,而感染后不处理或用诱导剂处理则不产生抗性。本报告证明了化学控制的抗病性,并证实了蜕皮激素激动剂诱导系统在温室条件下的实用性。