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松针散斑壳,一种森林病原体,含有黄曲霉毒素生物合成途径基因的同源物。

Dothistroma pini, a forest pathogen, contains homologs of aflatoxin biosynthetic pathway genes.

作者信息

Bradshaw Rosie E, Bhatnagar Deepak, Ganley Rebecca J, Gillman Carmel J, Monahan Brendon J, Seconi Janet M

机构信息

Institute of Molecular Biosciences, Massey University, Palmerston North, New Zealand.

出版信息

Appl Environ Microbiol. 2002 Jun;68(6):2885-92. doi: 10.1128/AEM.68.6.2885-2892.2002.

Abstract

Homologs of aflatoxin biosynthetic genes have been identified in the pine needle pathogen Dothistroma pini. D. pini produces dothistromin, a difuranoanthraquinone toxin with structural similarity to the aflatoxin precursor versicolorin B. Previous studies with purified dothistromin suggest a possible role for this toxin in pathogenicity. By using an aflatoxin gene as a hybridization probe, a genomic D. pini clone was identified that contained four dot genes with similarity to genes in aflatoxin and sterigmatocystin gene clusters with predicted activities of a ketoreductase (dotA), oxidase (dotB), major facilitator superfamily transporter (dotC), and thioesterase (dotD). A D. pini dotA mutant was made by targeted gene replacement and shown to be severely impaired in dothistromin production, confirming that dotA is involved in dothistromin biosynthesis. Accumulation of versicolorin A (a precursor of aflatoxin) by the dotA mutant confirms that the dotA gene product is involved in an aflatoxin-like biosynthetic pathway. Since toxin genes have been found to be clustered in fungi in every case analyzed so far, it is speculated that the four dot genes may comprise part of a dothistromin biosynthetic gene cluster. A fifth gene, ddhA, is not a homolog of aflatoxin genes and could be at one end of the dothistromin cluster. These genes will allow comparative biochemical and genetic studies of the aflatoxin and dothistromin biosynthetic pathways and may also lead to new ways to control Dothistroma needle blight.

摘要

在松针病原菌松针散斑壳(Dothistroma pini)中已鉴定出黄曲霉毒素生物合成基因的同源物。松针散斑壳产生多杀霉素,这是一种二呋喃蒽醌毒素,其结构与黄曲霉毒素前体杂色曲霉素B相似。先前对纯化的多杀霉素的研究表明,这种毒素在致病性方面可能发挥作用。通过使用黄曲霉毒素基因作为杂交探针,鉴定出一个松针散斑壳基因组克隆,该克隆包含四个dot基因,它们与黄曲霉毒素和柄曲霉素基因簇中的基因相似,预测具有酮还原酶(dotA)、氧化酶(dotB)、主要易化子超家族转运蛋白(dotC)和硫酯酶(dotD)的活性。通过靶向基因替换构建了一个松针散斑壳dotA突变体,结果表明该突变体在多杀霉素产生方面严重受损,证实dotA参与多杀霉素的生物合成。dotA突变体中杂色曲霉素A(黄曲霉毒素的前体)的积累证实dotA基因产物参与了类似黄曲霉毒素的生物合成途径。由于迄今为止在分析的每种真菌中都发现毒素基因是成簇存在的,因此推测这四个dot基因可能是多杀霉素生物合成基因簇的一部分。第五个基因ddhA不是黄曲霉毒素基因的同源物,可能位于多杀霉素簇的一端。这些基因将有助于对黄曲霉毒素和多杀霉素生物合成途径进行比较生化和遗传研究,也可能会带来控制松针散斑病的新方法。

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