Proctor R H, Hohn T M, McCormick S P, Desjardins A E
Mycotoxin Research Unit, National Center for Agricultural Utilization Research, USDA Agricultural Research Service, Peoria, Illinois 61604-3902, USA.
Appl Environ Microbiol. 1995 May;61(5):1923-30. doi: 10.1128/aem.61.5.1923-1930.1995.
In Fusarium sporotrichioides, several genes required for biosynthesis of the trichothecene mycotoxin T-2 toxin are closely linked. Further characterization of this gene cluster has revealed a gene, Tri6, that specifies a 217-amino-acid protein with regions similar to Cys2His2 zinc finger proteins. Temporal expression of Tri6 is similar to that of trichothecene biosynthetic pathway genes. Analysis of Tri6 transcripts indicated that transcription is initiated in two regions and that within each region there may be at least four initiation sites. Disruption of Tri6 resulted in a mutant that did not produce trichothecenes but that did accumulate low levels of the trichothecene precursor trichodiene. The Tri6 mutant was unable to convert six trichothecene biosynthetic intermediates to T-2 toxin, and transcription of two biosynthetic genes, Tri4 and Tri5, was greatly reduced in the mutant relative to the wild type. In addition, the product of Tri6 functioned as a transcriptional activator in Saccharomyces cerevisiae when fused to the DNA binding region of GAL4. These results indicate that Tri6 encodes a protein involved in the transcriptional regulation of trichothecene biosynthetic genes in F. sporotrichioides.
在拟枝孢镰刀菌中,单端孢霉烯族毒素T-2毒素生物合成所需的几个基因紧密连锁。对该基因簇的进一步表征揭示了一个基因Tri6,它编码一种217个氨基酸的蛋白质,其区域与Cys2His2锌指蛋白相似。Tri6的时间表达与单端孢霉烯族毒素生物合成途径基因的表达相似。对Tri6转录本的分析表明,转录起始于两个区域,并且在每个区域内可能至少有四个起始位点。Tri6的破坏导致一个突变体,该突变体不产生单端孢霉烯族毒素,但确实积累了低水平的单端孢霉烯族毒素前体 trichodiene。Tri6突变体无法将六种单端孢霉烯族毒素生物合成中间体转化为T-2毒素,并且相对于野生型,突变体中两个生物合成基因Tri4和Tri5的转录大大减少。此外,当与GAL4的DNA结合区域融合时,Tri6的产物在酿酒酵母中起转录激活剂的作用。这些结果表明,Tri6编码一种参与拟枝孢镰刀菌中单端孢霉烯族毒素生物合成基因转录调控的蛋白质。