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首页> 外文期刊>Toxins >Control of Aflatoxin Production of Aspergillus flavus and Aspergillus parasiticus Using RNA Silencing Technology by Targeting aflD (nor-1) Gene
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Control of Aflatoxin Production of Aspergillus flavus and Aspergillus parasiticus Using RNA Silencing Technology by Targeting aflD (nor-1) Gene

机译:通过靶向aflD(nor-1)基因的RNA沉默技术控制黄曲霉黄曲霉和寄生曲霉黄曲霉毒素的生产

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Aspergillus flavus and Aspergillus parasiticus are important pathogens of cotton, corn, peanuts and other oil-seed crops, producing toxins both in the field and during storage. We have designed three siRNA sequences (Nor-Ia, Nor-Ib, Nor-Ic) to target the mRNA sequence of the aflD gene to examine the potential for using RNA silencing technology to control aflatoxin production. Thus, the effect of siRNAs targeting of two key genes in the aflatoxin biosynthetic pathway, aflD (structural) and aflR (regulatory gene) and on aflatoxin B1 (AFB1), and aflatoxin G1 (AFG1) production was examined. The study showed that Nor-Ib gave a significant decrease in aflD mRNA, aflR mRNA abundance, and AFB1 production (98, 97 and 97% when compared to the controls) in A. flavus NRRL3357, respectively. Reduction in aflD and aflR mRNA abundance and AFB1 production increased with concentration of siRNA tested. There was a significant inhibition in aflD and AFB1 production by A. flavus EGP9 and AFG1 production by A. parasiticus NRRL 13005. However, there was no significant decrease in AFG1 production by A. parasiticus SSWT 2999. Changes in AFB1 production in relation to mRNA levels of aflD showed a good correlation (R = 0.88; P = 0.00001); changes in aflR mRNA level in relation to mRNA level of aflD also showed good correlation (R = 0.82; P = 0.0001). The correlations between changes in aflR and aflD gene expression suggests a strong relationship between these structural and regulatory genes, and that aflD could be used as a target gene to develop efficient means for aflatoxin control using RNA silencing technology.
机译:黄曲霉和寄生曲霉是棉花,玉米,花生和其他油料作物的重要病原体,在田间和储存过程中均产生毒素。我们设计了三个siRNA序列(Nor-Ia,Nor-Ib,Nor-Ic)来靶向aflD基因的mRNA序列,以检验使用RNA沉默技术控制黄曲霉毒素生产的潜力。因此,siRNA靶向黄曲霉毒素生物合成途径中的两个关键基因aflD(结构)和aflR(调节基因)以及对黄曲霉毒素B 1 (AFB 1 )的影响,并检查了黄曲霉毒素G 1 (AFG 1 )的产生。研究表明,Nor-Ib分别使黄曲霉NRRL3357的aflD mRNA,aflR mRNA丰度和AFB 1 产生显着降低(与对照相比分别为98%,97%和97%) 。 aflD和aflR mRNA丰度的减少以及AFB 1 的产生随所测试siRNA浓度的增加而增加。黄曲霉EGP9对aflD和AFB 1 的产生有明显的抑制作用,而副寄生曲霉NRRL 13005对AFG 1 的产生有抑制作用。寄生拟南芥SSWT 2999产生的 1 。AFB 1 产生的变化与aflD的mRNA水平相关,具有良好的相关性(R = 0.88; P = 0.00001); aflR mRNA水平相对于aflD mRNA水平的变化也显示出良好的相关性(R = 0.82; P = 0.0001)。 aflR和aflD基因表达变化之间的相关性表明这些结构基因和调节基因之间存在密切关系,并且aflD可以用作靶基因,以开发使用RNA沉默技术控制黄曲霉毒素的有效手段。

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