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转甜薯羽状斑驳马铃薯 Y 病毒外壳蛋白基因植物的同源依赖性病毒抗性:靶位特异性和转基因甲基化。

Homology-dependent virus resistance in transgenic plants with the coat protein gene of sweet potato feathery mottle potyvirus: target specificity and transgene methylation.

出版信息

Phytopathology. 1999 May;89(5):385-91. doi: 10.1094/PHYTO.1999.89.5.385.

Abstract

ABSTRACT Nicotiana benthamiana plants were transformed with the coat protein (CP) coding sequence and the 3' nontranslated region (NTR) of the severe strain of sweet potato feathery mottle potyvirus (SPFMV-S). Regenerated lines were screened for virus resistance using recombinant potato virus X (PVX) engineered to contain the sequence homologous to the transgene. Out of 19 transgenic lines, 7 showed virus resistance after inoculation by the recombinant PVX. In most of the resistant lines, relatively low steady-state accumulation of the CP gene mRNA and little or no protein products were observed, suggesting that the resistance was manifested by a post-transcriptional gene-silencing mechanism. The resistant lines could be divided into two groups according to the target specificity of the silencing mechanism; one group recognizing the 3' part of the transgene mRNA and the other not only the 3' part, but also the 5' and the central part of the transgene mRNA. Particular regions of the transgene corresponding to the RNA target in the resistant lines were differentially methylated compared with the transgene sequence in a susceptible line.

摘要

摘要 本研究将甘薯羽状斑驳马铃薯 Y 病毒(SPFMV-S)强毒株的外壳蛋白(CP)编码序列及其 3'非翻译区(NTR)导入甜叶悬钩子烟。利用含有与转基因序列同源序列的重组马铃薯 X 病毒(PVX)对再生植株进行病毒抗性筛选。在 19 个转基因株系中,有 7 个在接种重组 PVX 后表现出抗病毒性。在大多数抗性株系中,CP 基因 mRNA 的稳态积累水平较低,几乎检测不到蛋白产物,这表明抗性是由转录后基因沉默机制引起的。根据沉默机制的靶标特异性,这些抗性株系可分为两组;一组识别转基因 mRNA 的 3'部分,另一组不仅识别 3'部分,还识别转基因 mRNA 的 5'和中心部分。与敏感株系相比,抗性株系中转基因中与 RNA 靶标对应的特定区域发生了差异甲基化。

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