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Functional Characterization of Two Clustersof Brachypodium distachyon UDP-GlycosyltransferasesEncoding Putative Deoxynivalenol Detoxification Genes

机译:编码推定的脱氧雪腐烯醇解毒基因的两个短节霉UDP-糖基转移酶簇的功能表征

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摘要

Plant small-molecule UDP-glycosyltransferases (UGT) glycosylate a vast number of endogenous substances but also act in detoxification of metabolites produced by plant-pathogenic microorganisms. The ability to inactivate the Fusarium graminearum mycotoxin deoxynivalenol (DON) into DON-3-O-glucoside is crucial for resistance of cereals. We analyzed the UGT gene family of the monocot model species Brachypodium distachyon and functionally characterized two gene clusters containing putative orthologs of previously identified DON-detoxification genes from Arabidopsis thaliana and barley. Analysis of transcription showed that UGT encoded in both clusters are highly inducible by DON and expressed at much higher levels upon infection with a wild-type DON-producing F. graminearum strain compared with infection with a mutant deficient in DON production. Expression of these genes in a toxin-sensitive strain of Sac-charomyces cerevisiae revealed that only two B. distachyon UGT encoded by members of a cluster ofsix genes homologous to the DON-inactivating barley HvUGT13248 were able to convert DON into DON-3-O-glucoside. Also, a single copy gene from Sorghum bicolor orthologous to this cluster and one of three putative orthologs of rice exhibit this ability. Seemingly, the UGT genes undergo rapid evolution and changes in copy number, making it difficult to identify orthologs with conserved substrate specificity.
机译:植物小分子UDP-糖基转移酶(UGT)糖基化大量的内源性物质,但也对植物病原微生物产生的代谢产物进行解毒。将禾谷镰刀菌霉菌毒素脱氧雪腐酚(DON)灭活为DON-3-O-葡萄糖苷的能力对于谷物的抵抗力至关重要。我们分析了单子叶植物模型种Brachypodium distachyon的UGT基因家族,并在功能上表征了两个基因簇,其中包含先前鉴定的拟南芥和大麦的DON解毒基因的直向同源物。转录分析表明,在两个簇中编码的UGT均可被DON高度诱导,并且与被DON产生缺陷的突变体感染相比,在被野生型产生DON的禾本科镰刀菌菌株感染后,其表达水平要高得多。这些基因在酿酒酵母毒素敏感菌株中的表达表明,由与失活DON的大麦HvUGT13248同源的6个基因簇的成员编码的仅两个B. distachyon UGT能够将DON转化为DON-3-O -葡萄糖苷。同样,来自双色高粱的单拷贝基因与该簇直系同源,并且三个推定的水稻直系同源基因之一也显示出这种能力。貌似,UGT基因经历了快速进化和拷贝数变化,因此难以鉴定具有保守底物特异性的直向同源物。

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