aflJ在黄曲霉早期途径中间体黄曲霉毒素积累中的作用及调控。

W Du, G R Obrian, G A Payne
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引用次数: 51

摘要

aflJ位于与途径调控基因aflR相邻的黄曲霉毒素生物合成基因簇中,参与黄曲霉毒素的产生,但其功能尚不清楚。aflJ在黄曲霉毒素产生菌株86-10中的过度表达导致黄曲霉毒素升高。为了研究aflJ的功能和调控,将缺失整个生物合成簇的菌株649-1转化为报告基因构建体、表达构建体或cosmid克隆,并分析其基因表达或代谢物积累情况。过表达aflJ不会导致ver-1、omtA或aflR的转录升高。为了确定过表达aflJ是否会导致早期途径中间产物的增加,我们用cosmid 5E6和gpdA::aflJ单独、gpdA::aflR单独或aflJ和aflR一起转化菌株649-1。Cosmid 5E6包含pksA、nor-1、fas-1和fas-2基因,这些基因是早期途径中间体averantin的生物合成所必需的。单独含有5E6的649-1变形子不产生可检测到的averantin。相比之下,含有gpdA::aflR的5E6突变体产生平均蛋白,但仅为同时含有aflR和aflJ的突变体的一半。Northern blot分析显示,与仅含有gpdA::aflR的5E6转化子相比,同时含有aflR和aflJ的5E6转化子的pksA转录本和nor-1转录本分别增加了5倍和4倍。此外,aflJ的转录受aflR的调控。过表达aflR导致aflJ转录升高。aflJ似乎调节了黄曲霉毒素生物合成早期基因的调控。
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Function and regulation of aflJ in the accumulation of aflatoxin early pathway intermediate in Aspergillus flavus.

aflJ resides within the aflatoxin biosynthetic gene cluster adjacent to the pathway regulatory gene aflR and is involved in aflatoxin production, but its function is unknown. Over-expression of aflJ in the aflatoxin-producing strain 86-10 resulted in increased aflatoxin. In an effort to study the function and regulation of aflJ, strain 649-1 lacking the entire biosynthetic cluster was transformed with either reporter constructs, expression constructs, or cosmid clones and analysed for gene expression or metabolite accumulation. Over-expression of aflJ did not result in elevated transcription of ver-1, omtA or aflR. To determine if over-expression of aflJ leads to an increase in early pathway intermediates, strain 649-1 was transformed with cosmid 5E6 and either gpdA::aflJ alone, gpdA::aflR alone, or aflJ and aflR together. Cosmid 5E6 contains the genes pksA, nor-1, fas-1, and fas-2, which are required for the biosynthesis of the early pathway intermediate averantin. 649-1 transformants containing 5E6 alone produced no detectable averantin. In contrast, 5E6 transformants with gpdA::aflR produced averantin, but only half as much as those transformants containing both aflR and aflJ. Northern blot analysis showed that 5E6 transformants containing both aflR and aflJ had five times more pksA transcripts and four times more nor-1 transcripts than 5E6 transformants containing gpdA::aflR alone. Further, aflJ transcription was regulated by aflR. Over-expression of aflR resulted in elevated aflJ transcription. aflJ appears to modulate the regulation of early genes in aflatoxin biosynthesis.

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