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Physical and transcriptional map of an aflatoxin gene cluster in Aspergillus parasiticus and functional disruption of a gene involved early in the aflatoxin pathway.

机译:黄曲霉寄生虫中黄曲霉毒素基因簇的物理和转录图以及黄曲霉毒素途径早期涉及的基因的功能破坏。

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摘要

Two genes involved in aflatoxin B1 (AFB1) biosynthesis in Aspergillus parasiticus, nor-1 and ver-1, were localized to a 35-kb region on one A. parasiticus chromosome and to the genomic DNA fragment carried on a single cosmid, NorA. A physical and transcriptional map of the 35-kb genomic DNA insert in cosmid NorA was prepared to help determine whether other genes located in the nor-1-ver-1 region were involved in aflatoxin synthesis. Northern (RNA) analysis performed on RNA isolated from A. parasiticus SU1 grown in aflatoxin-inducing medium localized 14 RNA transcripts encoded by this region. Eight of these transcripts, previously unidentified, showed a pattern of accumulation similar to that of nor-1 and ver-1, suggesting possible involvement in AFB1 synthesis. To directly test this hypothesis, gene-1, encoding one of the eight transcripts, was disrupted in A. parasiticus CS10, which accumulates the aflatoxin precursor versicolorin A, by insertion of plasmid pAPNVES4. Thin-layer chromatography revealed that gene-1 disruptant clones no longer accumulated versicolorin A. Southern hybridization analysis of these clones indicated that gene-1 had been disrupted by insertion of the disruption vector. These data confirmed that gene-1 is directly involved in AFB1 synthesis. The predicted amino acid sequence of two regions of gene-1 showed a high degree of identity and similarity with the beta-ketoacyl-synthase and acyltransferase functional domains of polyketide synthases, consistent with a proposed role for gene-1 in polyketide backbone synthesis.
机译:寄生虫曲霉中黄曲霉毒素B1(AFB1)生物合成的两个基因nor-1和ver-1位于一个寄生虫曲霉染色体上的35kb区域,并位于单个粘粒NorA上携带的基因组DNA片段。制备了粘粒NorA中35-kb基因组DNA插入片段的物理和转录图,以帮助确定位于nor-1-ver-1区的其他基因是否参与黄曲霉毒素的合成。对从在黄曲霉毒素诱导培养基中生长的寄生曲霉SU1分离的RNA进行RNA的Northern(RNA)分析,定位该区域编码的14个RNA转录本。这些转录物中的八种以前未被发现,显示出类似于nor-1和ver-1的积累模式,表明可能参与了AFB1的合成。为了直接检验该假设,通过插入质粒pAPNVES4,在寄生曲霉CS10中破坏了编码八个转录物之一的基因-1,该曲霉CS10中积累了黄曲霉毒素前体versicolorinA。薄层色谱法表明,基因1破坏性克隆不再积累VersicolorinA。这些克隆的Southern杂交分析表明,基因1已通过插入破坏载体而被破坏。这些数据证实基因-1直接参与AFB1的合成。基因1的两个区域的预测的氨基酸序列与聚酮化合物合酶的β-酮酰基合酶和酰基转移酶功能域具有高度的同一性和相似性,与基因1在聚酮骨架合成中的拟议作用一致。

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