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首页> 外文期刊>Frontiers in Plant Science >Comparative genomics of Australian isolates of the wheat stem rust pathogen Puccinia graminis f. sp. tritici reveals extensive polymorphism in candidate effector genes
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Comparative genomics of Australian isolates of the wheat stem rust pathogen Puccinia graminis f. sp. tritici reveals extensive polymorphism in candidate effector genes

机译:澳大利亚分离出的小麦茎锈病病原体 Puccinia graminis 的比较基因组学。 sp。 tritici 揭示了候选效应基因的广泛多态性

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The wheat stem rust fungus Puccinia graminis f. sp. tritici ( Pgt ) is one of the most destructive pathogens of wheat. In this study, a draft genome was built for a founder Australian Pgt isolate of pathotype (pt.) 21-0 (collected in 1954) by next generation DNA sequencing. A combination of reference-based assembly using the genome of the previously sequenced American Pgt isolate CDL 75-36-700-3 (p7a) and de novo assembly were performed resulting in a 92 Mbp reference genome for Pgt isolate 21-0. Approximately 13 Mbp of de novo assembled sequence in this genome is not present in the p7a reference assembly. This novel sequence is not specific to 21-0 as it is also present in three other Pgt rust isolates of independent origin. The new reference genome was subsequently used to build a pan-genome based on five Australian Pgt isolates. Transcriptomes from germinated urediniospores and haustoria were separately assembled for pt. 21-0 and comparison of gene expression profiles showed differential expression in ~10% of the genes each in germinated spores and haustoria. A total of 1,924 secreted proteins were predicted from the 21-0 transcriptome, of which 520 were classified as haustorial secreted proteins (HSPs). Comparison of 21-0 with two presumed clonal field derivatives of this lineage (collected in 1982 and 1984) that had evolved virulence on four additional resistance genes ( Sr5 , Sr11 , Sr27 , SrSatu ) identified mutations in 25 HSP effector candidates. Some of these mutations could explain their novel virulence phenotypes.
机译:小麦茎锈病真菌Puccinia graminis f。 sp。小麦是小麦中最具破坏力的病原体之一。在这项研究中,通过下一代DNA测序为病原体(pt。)21-0的创始澳大利亚Pgt分离株构建了基因组草图。使用先前测序的美国Pgt分离物CDL 75-36-700-3(p7a)的基因组进行基于参考的组装和从头组装,从而产生了Pgt分离物21-0的92 Mbp参考基因组。 p7a参考装配中不存在该基因组中约13 Mbp的从头装配序列。这个新序列对21-0并不特异,因为它也存在于其他三个独立来源的Pgt锈菌分离物中。新的参考基因组随后被用于基于五种澳大利亚Pgt分离株构建一个全基因组。来自发芽的双孢子虫和haustoria的转录组分别组装用于pt。 21-0和基因表达谱的比较表明,发芽孢子和黑麦芽孢杆菌中约有10%的基因表达差异。从21-0转录组中预测总共有1,924个分泌蛋白,其中520个被归类为空泡分泌蛋白(HSP)。将21-0与该谱系的两个假定克隆场衍生物(分别收集于1982年和1984年)进行比较,该衍生物在四个其他抗性基因(Sr5,Sr11,Sr27,SrSatu)上已产生了毒力,从而鉴定出25个HSP效应子候选物中的突变。这些突变中的一些可以解释其新颖的毒力表型。

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