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首页> 外文期刊>Molecular Plant-Microbe Interactions >Gain of Virulence on Rsv1-Genotype Soybean by an Avirulent Soybean mosaic virus Requires Concurrent Mutations in Both P3 and HC-Pro
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Gain of Virulence on Rsv1-Genotype Soybean by an Avirulent Soybean mosaic virus Requires Concurrent Mutations in Both P3 and HC-Pro

机译:通过无毒大豆花叶病毒获得Rsv1基因型大豆的毒力需要同时发生P3和HC-Pro突变

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摘要

In soybean, Rsv1 , a single dominant resistance gene, invokes extreme resistance (ER) against most Soybean mosaic virus (SMV) strains, including SMV-N, but not SMV-G7, which provokes a virulent lethal systemic hypersensitive response (LSHR). The elicitor functions of the two viruses provoking Rsv1 -mediated ER and LSHR have been mapped to the N-terminal 271 amino acids of P3 from SMV-N and SMV-G7, respectively, which differ by nine residues between the two strains. To identify amino acids of P3 from SMV-N provoking Rsv1 -mediated ER, the unique residues of SMV-G7 were substituted with those of SMV-N. Of the mutants tested on Rsv1 -genotype soybean, only SMV-G7I788R and SMV-G7T948A lost virulence. However, substitution of amino acids of SMV-N, individually or in combination, with the reciprocal residues from SMV-G7 at these two positions failed to confer virulence to SMV-N. In the search for additional virulence determinants, a series of SMV-N chimeras was generated in which fragments within a region from near the middle of the helper-component proteinase (HC-Pro) cistron to the 5′ end of the cytoplasmic inclusion cistron, nucleotides 1,605 to 3,787, were replaced with those of SMV-G7. Only SMV-N-derived chimeras harboring the 3′ region of HC-Pro, at least from nucleotide 2,013, and the entire 5′ end of P3 (nucleotides 2,430 to 3,237) from SMV-G7 were virulent whereas reciprocal exchanges resulted in loss of SMV-G7 virulence. This region of HC-Pro differs by three amino acids between SMV-N and SMV-G7. Analyses of SMV-G7-derived HC-Pro site-directed mutants showed that only SMV-G7M683R lost virulence on Rsv1 -genotype soybean; however, SMV-NR682M failed to gain virulence. Nevertheless, an SMV-N derived mutant with three concurrent substitutions, R682M+R787I+A947T, gained virulence. The data indicate that both P3 and HC-Pro are involved in virulence of SMV on Rsv1 -genotype soybean.
机译:在大豆中,单一的显性抗性基因Rsv1对大多数大豆花叶病毒(SMV)菌株(包括SMV-N,而不是SMV-G7)产生极强的抗性(ER),后者会引起致命的致命的系统性超敏反应(LSHR)。两种引起Rsv1介导的ER和LSHR的病毒的激发子功能已分别定位于SMV-N和SMV-G7的P3的N端271个氨基酸,这两个菌株之间相差9个残基。为了从引起Rsv1介导的ER的SMV-N中鉴定出P3的氨基酸,将SMV-G7的独特残基替换为SMV-N的残基。在Rsv1基因型大豆上测试的突变体中,只有SMV-G7 I788R 和SMV-G7 T948A 丧失了毒力。然而,用这两个位置的SMV-G7的相反残基单独或组合取代SMV-N的氨基酸不能赋予SMV-N以毒力。在寻找其他毒力决定因素时,产生了一系列SMV-N嵌合体,其中片段从辅助成分蛋白酶(HC-Pro)顺反子的中部附近到胞质内含顺反子的5'端,用SMV-G7取代了核苷酸1,605至3,787。只有SHC-Pro的3'区域(至少来自核苷酸2,013)和SMV-G7的P3的5'端(核苷酸2,430至3,237)的SMV-N衍生嵌合体才具有毒性,而相互交换导致丧失SMV-G7毒力。 HC-Pro的此区域在SMV-N和SMV-G7之间相差三个氨基酸。 SMV-G7衍生的HC-Pro定点突变体的分析表明,只有SMV-G7 M683R 对Rsv1基因型大豆失去了毒力。但是,SMV-N R682M 无法获得毒力。然而,具有三个同时取代的SMV-N衍生突变体R682M + R787I + A947T获得了毒力。数据表明P3和HC-Pro均与Rsv1基因型大豆上的SMV毒力有关。

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