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首页> 外文期刊>DNA research: an international journal for rapid publication of reports on genes and genomes >Comparative Gene Expression Analysis of Susceptible and Resistant Near-Isogenic Lines in Common Wheat Infected by Puccinia triticina
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Comparative Gene Expression Analysis of Susceptible and Resistant Near-Isogenic Lines in Common Wheat Infected by Puccinia triticina

机译:小麦被小麦锈病感染后易感和抗近等基因系的比较基因表达分析

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Gene expression after leaf rust infection was compared in near-isogenic wheat lines differing in the Lr10 leaf rust resistance gene. RNA from susceptible and resistant plants was used for cDNA library construction. In total, 55 008 ESTs were sequenced from the two libraries, then combined and assembled into 14 268 unigenes for further analysis. Of these ESTs, 89% encoded proteins similar to (E value of ≤10?5) characterized or annotated proteins from the NCBI non-redundant database representing diverse molecular functions, cellular localization and biological processes based on gene ontology classification. Further, the unigenes were classified into susceptible and resistant classes based on the EST members assembled from the respective libraries. Several genes from the resistant sample (14-3-3 protein, wali5 protein, actin-depolymerization factor and ADP-ribosylation factor) and the susceptible sample (brown plant hopper resistance protein, caffeic acid O-methyltransferase, pathogenesis-related protein and senescence-associated protein) were selected and their differential expression in the resistant and susceptible samples collected at different time points after leaf rust infection was confirmed by RT–PCR analysis. The molecular pathogenicity of leaf rust in wheat was studied and the EST data generated made a foundation for future studies.
机译:比较了Lr10叶片抗锈性基因不同的近等基因小麦品系中叶片锈蚀感染后的基因表达。来自易感和抗性植物的RNA被用于cDNA文库的构建。总共,从这两个文库中测序了55 008个EST,然后合并并组装成14 268个单基因,用于进一步分析。在这些EST中,有89%编码的蛋白质(E值≤10?5 )与NCBI非冗余数据库中表征或注释的蛋白质相似,这些蛋白质代表多种分子功能,细胞定位和基于基因的生物学过程本体分类。此外,根据从各个文库中组装的EST成员,将单基因分为易感和抗性类别。耐药样品中的几个基因(14-3-3蛋白,wali5蛋白,肌动蛋白解聚因子和ADP核糖基化因子)和易感样品(褐飞虱抗性蛋白,咖啡酸O-甲基转移酶,致病相关蛋白和衰老)选择相关蛋白),并通过RT-PCR分析确认其在叶锈病感染后不同时间点采集的抗性和易感样品中的差异表达。研究了小麦叶锈病的分子致病性,并获得了EST数据,为今后的研究奠定了基础。

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