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瑞氏木霉 C2H2 锌指转录因子 Rua1 激活玉米黑粉菌 ustilagic 酸生物合成基因簇。

Activation of the ustilagic acid biosynthesis gene cluster in Ustilago maydis by the C2H2 zinc finger transcription factor Rua1.

机构信息

Philipps University Marburg, Dept. of Biology, Karl-von-Frisch-Str. 8, D-35032 Marburg, Germany.

出版信息

Appl Environ Microbiol. 2010 Apr;76(8):2633-40. doi: 10.1128/AEM.02211-09. Epub 2010 Feb 19.

Abstract

The phytopathogenic basidiomycetous fungus Ustilago maydis secretes, under conditions of nitrogen starvation, large amounts of the biosurfactant ustilagic acid (UA). This secreted cellobiose glycolipid is toxic for many microorganisms and confers biocontrol activity to U. maydis. Recently, a large gene cluster that is responsible for UA biosynthesis was identified. Here, we show that expression of all cluster genes depends on Rua1, a nuclear protein of the C(2)H(2) zinc finger family, whose gene is located within the gene cluster. While deletion of rua1 results in complete loss of UA production, overexpression of rua1 promotes increased UA synthesis even in the presence of a good nitrogen source. Bioinformatic analysis allowed us to identify a conserved sequence element that is present in the promoters of all structural genes involved in UA biosynthesis. Deletion analysis of several promoters within the cluster revealed that this DNA element serves as an upstream activating sequence (UAS) and mediates Rua1-dependent expression. We used the yeast one-hybrid system to demonstrate specific recognition of this DNA element by Rua1. Introduction of nucleotide exchanges into the consensus sequence interfered with Rua1-dependent activation, suggesting that this sequence element acts as a direct binding site for Rua1.

摘要

植物病原担子菌玉米黑粉菌在氮饥饿条件下会分泌大量生物表面活性剂玉米赤霉酸(UA)。这种分泌的纤维二糖糖脂对许多微生物有毒,赋予玉米黑粉菌生物防治活性。最近,一个负责 UA 生物合成的大型基因簇被鉴定出来。在这里,我们表明,所有簇基因的表达都依赖于 Rua1,这是一种 C(2)H(2)锌指家族的核蛋白,其基因位于基因簇内。虽然 rua1 的缺失导致 UA 产量完全丧失,但 rua1 的过表达即使在有良好氮源的情况下也能促进 UA 合成的增加。生物信息学分析使我们能够识别出参与 UA 生物合成的所有结构基因启动子中存在的保守序列元件。对簇内的几个启动子进行缺失分析表明,这个 DNA 元件作为一个上游激活序列(UAS),介导 Rua1 依赖的表达。我们使用酵母单杂交系统证明了 Rua1 对这个 DNA 元件的特异性识别。将核苷酸交换引入到共识序列中干扰了 Rua1 依赖的激活,表明这个序列元件作为 Rua1 的直接结合位点发挥作用。

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