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花椰菜花叶病毒开放阅读框I和IV表达中双重策略的证据。

Evidence for a dual strategy in the expression of cauliflower mosaic virus open reading frames I and IV.

作者信息

Kobayashi K, Tsuge S, Nakayashiki H, Mise K, Furusawa I

机构信息

Laboratory of Plant Pathology, Faculty of Agriculture, Kyoto University, Japan.

出版信息

Microbiol Immunol. 1998;42(4):329-34. doi: 10.1111/j.1348-0421.1998.tb02291.x.

Abstract

Studies have indicated that cauliflower mosaic virus (CaMV) gene expression is mediated by the translation of polycistronic 35S pregenomic RNA, but the involvement of some minor subgenomic RNA species is also suspected. We examined the involvement of the 35S promoter in the expression of CaMV open reading frames (ORFs) I and IV using both 35S RNA-driven and promoter-less ORF I- and ORF IV-beta-glucuronidase (GUS) fusion constructs. In addition to the 35S promoter-dependent expression of both ORF I- and IV-GUS fusions, we detected the 35S promoter-independent expression of both fusion genes via subgenomic mRNAs, which were detected by Northern blotting in the protoplasts transfected with the 35S promoter-driven constructs as well as in those transfected with the promoter-less constructs. These results suggest the involvement of subgenomic RNAs in the expression of CaMV ORFs I and IV, and the operation of a dual strategy in the expression of two viral genes.

摘要

研究表明,花椰菜花叶病毒(CaMV)基因表达由多顺反子35S前基因组RNA的翻译介导,但也有人怀疑一些较小的亚基因组RNA种类也参与其中。我们使用35S RNA驱动的和无启动子的ORF I-和ORF IV-β-葡萄糖醛酸酶(GUS)融合构建体,研究了35S启动子在CaMV开放阅读框(ORF)I和IV表达中的作用。除了ORF I-和IV-GUS融合体的35S启动子依赖性表达外,我们还通过亚基因组mRNA检测到了两个融合基因的35S启动子非依赖性表达,在用35S启动子驱动构建体转染的原生质体以及用无启动子构建体转染的原生质体中,通过Northern印迹法检测到了亚基因组mRNA。这些结果表明亚基因组RNA参与了CaMV ORF I和IV的表达,以及两种病毒基因表达中的双重策略的运作。

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