Zijlstra C., Hohn T.
Friedrich Miescher-Institut, P.O. Box 2543, CH-4002 Basel, Switzerland.
Plant Cell. 1992 Dec;4(12):1471-1484. doi: 10.1105/tpc.4.12.1471.
Transformed Arabidopsis plants were used to study the effect of the cauliflower mosaic virus (CaMV) inclusion body protein on translation of dicistronic RNA. Reporter plants contain a dicistronic transcription unit with CaMV open reading frame VII (ORF VII) as the first and the [beta]-glucuronidase (GUS) reporter ORF as the second cistron. "Transactivator plants" contain CaMV ORF VI under the control of the strong CaMV 35S promoter. The transactivator plants were difficult to regenerate and showed an abnormal phenotype. Expression of GUS activity in the reporter plants was very low, but high GUS activity could be induced by introduction of gene VI, either by crossing with plants containing gene VI as a transgene or by infection with CaMV. Histological GUS assays showed that transactivation occurred in all types of tissue and at all developmental stages. The practical implications of the induction of GUS expression from the dicistronic unit by virus infection are discussed.
利用转化的拟南芥植株研究花椰菜花叶病毒(CaMV)包涵体蛋白对双顺反子RNA翻译的影响。报告植株含有一个双顺反子转录单元,其中CaMV开放阅读框VII(ORF VII)作为第一个顺反子,β-葡萄糖醛酸酶(GUS)报告基因开放阅读框作为第二个顺反子。“反式激活植株”在强CaMV 35S启动子的控制下含有CaMV ORF VI。反式激活植株难以再生,并表现出异常表型。报告植株中GUS活性的表达非常低,但通过引入基因VI可诱导高GUS活性,方法是与作为转基因含有基因VI的植株杂交或用CaMV感染。组织学GUS分析表明,反式激活发生在所有类型的组织和所有发育阶段。本文讨论了病毒感染从双顺反子单元诱导GUS表达的实际意义。