系列转移诱导的非产黄曲霉寄生的黄曲霉毒素调控因子分析。

S P Kale, J W Cary, N Hollis, J R Wilkinson, D Bhatnagar, J Yu, T E Cleveland, J W Bennett
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引用次数: 18

摘要

黄曲霉毒素(AFs)是寄生曲霉的致癌次生代谢产物。在以往的研究中,寄生蜂的非产毒性sec-(次级代谢阴性)变异是通过产毒性sec+(次级代谢阳性)亲本的菌丝连续转移产生的,用于遗传和生理分析,以了解AF生物合成的调控。先前的研究表明,在sec+和sec-菌株中,aflR的DNA序列没有差异,aflR是AF产生的正调节因子。本研究分析了AF的另一个正调节因子AflJ、次级代谢的全局调节因子laeA以及aflR和AflJ之间的基因间区域,以确定它们是否在sec表型的建立中起作用。研究表明,虽然该序列的同一性扩展到aflJ和aflJ-aflR基因间区,但sec-株中aflR的表达量比sec+株低几倍,而aflJ在sec-株中几乎没有表达。Western blot分析表明,该菌株虽然含有AflR蛋白,但不产生毒素。在第二株中引入第二拷贝aflR增加了aflR的表达,但没有恢复AF的产生。反转录pcr分析表明,laeA在sec+和sec-菌株中均有表达。这些结果表明,虽然aflR、aflJ和laeA是AF产生的必要条件,但它们并不充分。我们认为,aflR和aflJ的表达可能受到laeA下游的元件或不受laeA影响的通路的调控。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Analysis of aflatoxin regulatory factors in serial transfer-induced non-aflatoxigenic Aspergillus parasiticus.

Aflatoxins (AFs) are carcinogenic secondary metabolites of Aspergillus parasiticus. In previous studies, non-toxigenic A. parasiticus sec- (for secondary metabolism negative) variants were generated through serial transfer of mycelia from their toxigenic sec+ (for secondary metabolism positive) parents for genetic and physiological analysis for understanding regulation of AF biosynthesis. Previous studies have shown no difference in the DNA sequence of aflR, a positive regulator of AF production, in the sec+ and sec- strains. In this study, AflJ, another positive regulator of AF production, laeA, a global regulator of secondary metabolism, and the intergenic region between aflR and aflJ, were analysed to determine if they play a role in establishment of the sec- phenotype. The study showed that while this sequence identity extended to the aflJ as well as the aflJ-aflR intergenic region, expression of aflR in the sec- strain was several fold lower than that observed in the sec+ strain, while aflJ expression was barely detectable in the sec- strain. Western blot analysis indicated that despite AflR protein being present in the sec- strain, no toxin production resulted. Introduction of a second copy of aflR into the sec- strain increased aflR expression, but did not restore AF production. Lastly, reverse transcription-PCR analysis revealed that laeA was expressed in both sec+ and sec- strains. These results suggest that although aflR, aflJ and laeA are necessary for AF production, they are not sufficient. We propose that the aflR and aflJ expression may be regulated by element(s) downstream from laeA or from pathways not influenced by laeA.

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