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首页> 外文期刊>Molecular Plant Pathology >Altered trichothecene biosynthesis in TRI6-silenced transformants of Fusarium culmorum influences the severity of crown and foot rot on durum wheat seedlings
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Altered trichothecene biosynthesis in TRI6-silenced transformants of Fusarium culmorum influences the severity of crown and foot rot on durum wheat seedlings

机译:改变单端孢霉烯生物合成的镰culmorum TRI6-silenced转化株皇冠和腐蹄病的严重程度的影响硬质小麦幼苗

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摘要

An RNA silencing construct was used to alter mycotoxin production in the plant pathogenic fungus Fusarium culmorum, the incitant of crown and foot rot on wheat. The transformation of a wild-type strain and its nitrate reductase-deficient mutant with inverted repeat transgenes (IRTs) containing sequences corresponding to the trichothecene regulatory gene TRI6 was achieved using hygromycin B resistance as a selectable marker. Southern analysis revealed a variety of integration patterns of the TRI6 IRT. One transformant underwent homologous recombination with deletion of the endogenous TRI6 gene, whereas, in another transformant, the TRI6 IRT was not integrated into the genome. The TRI6 IRT did not alter the physiological characteristics, such as spore production, pigmentation or growth rate, on solid media. In most transformants, a high TRI6 amplification signal was detected by quantitative reverse transcription-polymerase chain reaction, corresponding to a TRI6-hybridizing smear of degraded fragments by Northern analysis, whereas TRI5 expression decreased compared with the respective non-transformed strain. Four transformants showed increased TRI5 expression, which was correlated with a dramatic (up to 28-fold) augmentation of deoxynivalenol production. Pathogenicity assays on durum wheat seedlings confirmed that impairment of deoxynivalenol production in the TRI6 IRT transformants correlated with a loss of virulence, with decreased disease indices ranging from 40% to 80% in nine silenced strains, whereas the overproducing transformants displayed higher virulence compared with the wild-type.
机译:RNA沉默构造用于改变在植物病原真菌毒素生产真菌镰刀菌素culmorum,皇冠的兴奋剂和小麦根腐病。野生型菌株及其硝酸reductase-deficient突变与反向重复转基因(红外热成像)包含序列单端孢霉烯对应监管基因TRI6通过使用潮霉素B电阻作为一个可选的标记。分析显示不同的集成TRI6红外热成像模式。经历了同源重组与删除内生TRI6基因,而在另一个转化株,TRI6红外热成像不集成基因组。生理特征,如孢子生产、色素沉着或增长率,固体媒体。放大信号被定量检测逆转录-聚合酶链反应,对应于一个TRI6-hybridizing涂片通过北部分析降解片段,而TRI5表达而下降各自的非转换压力。转化株显示增加TRI5表达式,这是与一个戏剧性的(deoxynivalenol 28-fold)增加生产。幼苗确认减值准备TRI6 deoxynivalenol生产红外热成像转化株与损失有关毒性,减少疾病指数等在九沉默菌株从40%降至80%,而显示的高产转化株高与野生型相比毒性。

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