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Expression of pathogenesis-related genes in cotton stems in response toinfection by Verticillium dahliae

机译:棉花黄萎病菌感染后病原相关基因在棉花茎中的表达

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The levels of mRNA transcripts of genes for several pathogenesis-related proteins were examined in cotton stems after infection of the plants with the soil-borne, vascular wilt pathogen Verticillium dahliae. Reverse transcription PCR sas used to estimate mRNA levels corresponding to particular transcripts. In order ro determine if differences in timing or level a of gene activation were likely to account for differences in the susceptibility of Gossypium hirsutum cultivars to Verticillium wilt, we compared the gene activation patterns in the relatively resistant commercial cultivar, Sicala V2 with those exhibited by the susceptible cultivar. CS50. A non-defoliating, Australian isolate of V. dahliae was used and infection was achieved by stempuncture inoculation with a conidial suspension of the pathogen. Levels of mRNA for genes for cadinene synthase, acidic chitinase, basic chitinase, beta -1,3-glucanase, and at least orle member of the family of cotton Ypr10 gene homologues coding ibr potential PRIG proteins increased after inoculation with V. dahliae, while levels of mRNA for a gene for phenylalanine ammonia lyase were similar in all samples. Even though leaf necrosis symptoms were found to be less severe in Sicala V2 after V. dahliae infection, no differences in the timing or in the extent or activation of gene repression were observed between the two cultivars used. Significant activation was not observed after treatment of CS50 with bion(R) (benzo-(1,2,3)- thiadiazole-7-carbothioc acid S-methyl ester, BTH) or methyl jasmonate, but there was a reduction in the severity of leaf necrosis of both cultivars after bion(R) treatment, which was malgrinai in CS50 but clearly evident in Sicala V2. Thus the enhanced partial resistance of cotton to Verticillium wilt observed here, whether due to cultivar or bion(R) treatment, is not accompanied by a change in the tinting or levels of expression of the genes investigated. Therefore it is: likely that some other factors are responsible For the degree of resistance observed.
机译:在棉花被土壤传播的枯萎病菌黄萎病菌侵染后,在棉花茎中检查了几种与病程相关的蛋白质的基因的mRNA转录水平。逆转录PCR用于估计对应于特定转录本的mRNA水平。为了确定基因激活时间或水平a的差异是否可能解释了陆地棉对黄萎病敏感性的差异,我们将相对抗性商品品种Sicala V2的基因激活模式与易感品种CS50。使用澳大利亚的大丽花弧菌的无叶分离株,并通过用病原体的分生孢子悬浮液进行穿刺接种来实现感染。接种大丽花弧菌后,卡丁烯合酶,酸性几丁质酶,碱性几丁质酶,β-1,3-葡聚糖酶和至少一个棉质Ypr10基因同源物家族成员中编码ibr潜在PRIG蛋白的基因的mRNA含量增加,而在所有样品中,苯丙氨酸解氨酶基因的mRNA水平均相似。尽管发现大丽花叶病毒感染后Sicala V2中的叶片坏死症状不那么严重,但是在使用的两个品种之间未观察到基因抑制的时机,程度或激活程度的差异。用bion®(苯并(1,2,3)-噻二唑-7-碳硫代酸S-甲酯,BTH)或茉莉酸甲酯处理CS50后,未观察到明显的活化作用,但严重程度有所降低bion(R)处理后两个品种叶片坏死的情况,在CS50中为麦格里尼,但在Sicala V2中明显。因此,在这里观察到的棉花对黄萎病的部分抗性增强,无论是由于栽培品种还是bion处理,都不会伴随着所研究基因的着色或表达水平的变化。因此,可能是:其他一些因素导致了观察到的抗药性。

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