黄曲霉和寄生蜂黄曲霉毒素合成机制研究的基因谱分析。

Jiujiang Yu, Catherine M Ronning, Jeffery R Wilkinson, Bruce C Campbell, Gary A Payne, Deepak Bhatnagar, Thomas E Cleveland, William C Nierman
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引用次数: 24

摘要

黄曲霉毒素是由某些真菌种类产生的有毒和致癌的多酮代谢产物,包括黄曲霉和寄生蜂。黄曲霉毒素的生物合成受到营养、环境等多种内外部因素的影响;因此,我们利用在不同条件下收获的菌丝构建的标准化cDNA表达文库中的表达序列标签(est)分析了黄曲霉的转录组。从26,110个cDNA克隆中共鉴定出7218条独特的ESTs。对这些est进行了功能分类,并确定了可能参与黄曲霉毒素污染过程的基因。基于这些EST序列信息,在基因组研究所(TIGR)构建了基因组DNA扩增子微阵列。为了确定控制食品和饲料中黄曲霉毒素污染的潜在调控网络,我们在黄曲霉毒素支持培养基和非黄曲霉毒素支持培养基中对黄曲霉和寄生蜂的基因表达谱进行了评估。在几种黄曲霉毒素支持介质中一致表达的基因有报道。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Gene profiling for studying the mechanism of aflatoxin biosynthesis in Aspergillus flavus and A. parasiticus.

Aflatoxins are toxic and carcinogenic polyketide metabolites produced by certain fungal species, including Aspergillus flavus and A. parasiticus. Many internal and external factors, such as nutrition and environment affect aflatoxin biosynthesis; therefore, we analyzed the transcriptome of A. flavus using expressed sequence tags (ESTs) from a normalized cDNA expression library constructed from mycelia harvested under several conditions. A total of 7218 unique ESTs were identified from 26,110 sequenced cDNA clones. Functional classifications were assigned to these ESTs and genes, potentially involved in the aflatoxin contamination process, were identified. Based on this EST sequence information, a genomic DNA amplicon microarray was constructed at The Institute for Genomic Research (TIGR). To identify potential regulatory networks controlling aflatoxin contamination in food and feeds, gene expression profiles in aflatoxin-supportive media versus non-aflatoxin-supportive media were evaluated in A. flavus and A. parasiticus. Genes consistently expressed in several aflatoxin-supportive media are reported.

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