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植物病原担子菌立枯丝核菌 AG4 的基因表达谱分析揭示了潜在的致病因子。

Gene expression profiling of the plant pathogenic basidiomycetous fungus Rhizoctonia solani AG 4 reveals putative virulence factors.

机构信息

Floral and Nursery Plants Research Unit, Beltsville Agricultural Research Center, USDA-ARS, Beltsville, MD 20705, USA.

出版信息

Mycologia. 2012 Sep-Oct;104(5):1020-35. doi: 10.3852/11-226. Epub 2012 Jul 9.

Abstract

Rhizoctonia solani is a ubiquitous basidiomycetous soilborne fungal pathogen causing damping-off of seedlings, aerial blights and postharvest diseases. To gain insight into the molecular mechanisms of pathogenesis a global approach based on analysis of expressed sequence tags (ESTs) was undertaken. To get broad gene-expression coverage, two normalized EST libraries were developed from mycelia grown under high nitrogen-induced virulent and low nitrogen/methylglucose-induced hypovirulent conditions. A pilot-scale assessment of gene diversity was made from the sequence analyses of the two libraries. A total of 2280 cDNA clones was sequenced that corresponded to 220 unique sequence sets or clusters (contigs) and 805 singlets, making up a total of 1025 unique genes identified from the two virulence-differentiated cDNA libraries. From the total sequences, 295 genes (38.7%) exhibited strong similarities with genes in public databases and were categorized into 11 functional groups. Approximately 61.3% of the R. solani ESTs have no apparent homologs in publicly available fungal genome databases and are considered unique genes. We have identified several cDNAs with potential roles in fungal pathogenicity, virulence, signal transduction, vegetative incompatibility and mating, drug resistance, lignin degradation, bioremediation and morphological differentiation. A codon-usage table has been formulated based on 14694 R. solani EST codons. Further analysis of ESTs might provide insights into virulence mechanisms of R. solani AG 4 as well as roles of these genes in development, saprophytic colonization and ecological adaptation of this important fungal plant pathogen.

摘要

立枯丝核菌是一种普遍存在的担子菌土壤病原真菌,可引起幼苗猝倒、气传病害和采后病害。为了深入了解致病的分子机制,我们采用基于表达序列标签(EST)分析的全局方法。为了广泛覆盖基因表达,我们根据在高氮诱导的毒力和低氮/甲基葡萄糖诱导的弱毒条件下生长的菌丝体,开发了两个标准化的 EST 文库。通过对这两个文库的序列分析,对基因多样性进行了初步评估。共对 2280 个 cDNA 克隆进行了测序,这些克隆对应于 220 个独特的序列集或簇(重叠群)和 805 个单核苷酸,从两个毒力分化的 cDNA 文库中总共鉴定了 1025 个独特的基因。在总序列中,有 295 个基因(38.7%)与公共数据库中的基因具有很强的相似性,被分为 11 个功能组。约 61.3%的立枯丝核菌 EST 在公共真菌基因组数据库中没有明显的同源物,被认为是独特的基因。我们已经鉴定出一些具有真菌致病性、毒力、信号转导、营养体不亲和性和交配、耐药性、木质素降解、生物修复和形态分化等潜在作用的 cDNA。根据 14694 个立枯丝核菌 EST 密码子制定了一个密码子使用表。对 EST 的进一步分析可能会深入了解立枯丝核菌 AG4 的毒力机制,以及这些基因在该重要真菌植物病原体的发育、腐生定殖和生态适应中的作用。

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