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A first genome assembly of the barley fungal pathogen?Pyrenophora teres?f.?teres

机译:大麦真菌病原体的第一个基因组组装?Pyrenophora teres?f。?teres

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Background: Pyrenophora teres f. teres is a necrotrophic fungal pathogen and the cause of one of barley's most important diseases, net form of net blotch. Here we report the first genome assembly for this species based solely on short Solexa sequencing reads of isolate 0-1. The assembly was validated by comparison to BAC sequences, ESTs, orthologous genes and by PCR, and complemented by cytogenetic karyotyping and the first genome-wide genetic map for P. teres f. teres. Results: The total assembly was 41.95 Mbp and contains 11,799 gene models of 50 amino acids or more. Comparison against two sequenced BACs showed that complex regions with a high GC content assembled effectively. Electrophoretic karyotyping showed distinct chromosomal polymorphisms between isolates 0-1 and 15A, and cytological karyotyping confirmed the presence of at least nine chromosomes. The genetic map spans 2477.7 c M and is composed of 243 markers in 25 linkage groups, and incorporates simple sequence repeat markers developed from the assembly. Among predicted genes, non-ribosomal peptide synthetases and efflux pumps in particular appear to have undergone a P. teres f. teres-specific expansion of non-orthologous gene families. Conclusions: This study demonstrates that paired-end Solexa sequencing can successfully capture coding regions of a filamentous fungal genome. The assembly contains a plethora of predicted genes that have been implicated in a necrotrophic lifestyle and pathogenicity and presents a significant resource for examining the bases for P. teres f. teres pathogenicity.
机译:背景:Pyrenophora teres f。 teres是一种坏死性真菌病原体,是大麦最重要的疾病之一,净斑点形式。在这里,我们仅基于短分离株0-1的Solexa测序读数报告了该物种的第一个基因组装配。通过与BAC序列,ESTs,直系同源基因的比较和PCR验证了该装配体,并补充了P. teres f。的细胞遗传核型和第一个全基因组遗传图谱。特雷斯。结果:总装配为41.95 Mbp,包含11799个50个氨基酸或更多氨基酸的基因模型。与两个测序BAC的比较表明,具有高GC含量的复杂区域可以有效地组装。电泳核型分析显示分离株0-1和15A之间存在明显的染色体多态性,细胞核型分析确认至少存在9条染色体。遗传图谱跨度为2477.7 c M,由25个连锁组中的243个标记组成,并整合了从装配中开发的简单序列重复标记。在预测的基因中,特别是非核糖体肽合成酶和外排泵似乎已经经历了对虾假单胞菌。非直系同源基因家族的特异扩增。结论:这项研究表明,双末端Solexa测序可以成功捕获丝状真菌基因组的编码区。该程序集包含大量的预测基因,这些基因与坏死性生活方式和致病性有关,并为检查假单胞菌的碱基提供了重要资源。致病性。

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