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鉴定感染大豆疫霉菌的毛果甘草叶片中的差异表达基因。

Identifying differentially expressed genes in leaves of Glycine tomentella in the presence of the fungal pathogen Phakopsora pachyrhizi.

机构信息

Department of Natural Resources and Environmental Sciences, University of Illinois, Urbana, IL 61821, USA.

出版信息

Planta. 2010 Oct;232(5):1181-9. doi: 10.1007/s00425-010-1251-5. Epub 2010 Aug 14.

Abstract

To compare transcription profiles in genotypes of Glycine tomentella that are differentially sensitive to soybean rust, caused by the fungal pathogen Phakopsora pachyrhizi, four cDNA libraries were constructed using the suppression subtractive hybridization method. Libraries were constructed from rust-infected and non-infected leaves of resistant (PI509501) and susceptible (PI441101) genotypes of G. tomentella, and subjected to subtractive hybridization. A total of 1,536 sequences were obtained from these cDNA libraries from which 195 contigs and 865 singletons were identified. Of these sequenced cDNA clones, functions of 646 clones (61%) were determined. In addition, 160 clones (15%) had significant homology to hypothetical proteins; while the remaining 254 clones (24%) did not reveal any hits. Of those 646 clones with known functions, different genes encoding protein products involved in metabolism, cell defense, energy, protein synthesis, transcription, and cellular transport were identified. These findings were subsequently confirmed by real time RT-PCR and dot blot hybridization.

摘要

为了比较感染和未感染大豆锈病(由真菌病原菌 Phakopsora pachyrhizi 引起)的不同敏感型甘蓝根瘤菌( Glycine tomentella )基因型的转录谱,使用抑制差减杂交法构建了四个 cDNA 文库。文库是从抗(PI509501)和感(PI441101)基因型甘蓝根瘤菌的感病和未感染叶片中构建的,并进行了差减杂交。从这些 cDNA 文库中获得了 1536 个序列,从中鉴定出 195 个重叠群和 865 个单序列。在这些测序的 cDNA 克隆中,确定了 646 个克隆(61%)的功能。此外,160 个克隆(15%)与假定蛋白具有显著同源性;而其余 254 个克隆(24%)没有任何命中。在具有已知功能的 646 个克隆中,鉴定出了不同的基因,这些基因编码参与代谢、细胞防御、能量、蛋白质合成、转录和细胞运输的蛋白产物。随后通过实时 RT-PCR 和点杂交验证了这些发现。

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