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对烟草花叶病毒的广泛抗性由一个经过修饰的烟草花叶病毒复制酶转基因介导。

Broad resistance to tobamoviruses is mediated by a modified tobacco mosaic virus replicase transgene.

作者信息

Donson J, Kearney C M, Turpen T H, Khan I A, Kurath G, Turpen A M, Jones G E, Dawson W O, Lewandowski D J

机构信息

Biosource Genetics Corporation, Vacaville, CA 95688.

出版信息

Mol Plant Microbe Interact. 1993 Sep-Oct;6(5):635-42. doi: 10.1094/mpmi-6-635.

Abstract

Tobacco plants made transgenic to express the wild type tobacco mosaic virus (TMV) 183-kDa replicase gene were not resistant to TMV. However, transgenic plants containing essentially the same sequences, but with an additional insertion that would terminate translation in the middle of the 183-kDa gene, were highly resistant to systemic infection by TMV and other tobamoviruses. The 1.4-kbp insertion in the replicase open reading frame (ORF) of the resistant plants was shown by DNA sequencing to be an IS10-like transposable element, which apparently inserted itself into the TMV sequence at nucleotide 2875 sometime during the propagation of this replicase ORF plasmid (pREP21). Because of four stop codons, in frame with the TMV replicase ORF on the immediate 5' border of the IS insertion, REP21 effectively represents domain 1 (putative methylase domain) and a portion of domain 2 (putative helicase domain) of the TMV replicase ORF. REP21 Xanthi tobacco plants had a level of resistance to TMV similar to other reported transgenic replicase plants. No TMV was detected in upper leaves of these plants at 1-mo postinoculation. In addition, REP21 plants were resistant to an unusually broad range of tobamoviruses including tomato mosaic virus, tobacco mild green mosaic virus, TMV-U5, green tomato atypical mosaic virus, and ribgrass mosaic virus. These plants were not resistant to cucumber mosaic cucumovirus. The lack of systemic infection by TMV was due to reduced multiplication in inoculated leaves rather than complete prevention of replication.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

经转基因改造以表达野生型烟草花叶病毒(TMV)183-kDa复制酶基因的烟草植株对TMV没有抗性。然而,含有基本相同序列但有一个额外插入片段(该插入片段会在183-kDa基因中部终止翻译)的转基因植株对TMV和其他烟草花叶病毒的系统感染具有高度抗性。通过DNA测序表明,抗性植株复制酶开放阅读框(ORF)中的1.4-kbp插入片段是一个类似IS10的转座元件,它显然在该复制酶ORF质粒(pREP21)的传播过程中的某个时候插入到了TMV序列的第2875个核苷酸处。由于有四个终止密码子,与IS插入片段紧邻的5'边界上的TMV复制酶ORF读框一致,REP21有效地代表了TMV复制酶ORF的结构域1(假定甲基化酶结构域)和结构域2的一部分(假定解旋酶结构域)。REP21黄花烟草植株对TMV的抗性水平与其他报道的转基因复制酶植株相似。接种后1个月,在这些植株的上部叶片中未检测到TMV。此外,REP21植株对异常广泛的烟草花叶病毒具有抗性,包括番茄花叶病毒、烟草轻绿花叶病毒、TMV-U5、绿色番茄非典型花叶病毒和长叶车前花叶病毒。这些植株对黄瓜花叶黄瓜病毒没有抗性。TMV缺乏系统感染是由于接种叶片中的增殖减少,而不是完全阻止复制。(摘要截断于250字)

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