Suppr超能文献

亚麻锈菌(Melampsora lini)易感感染期间诱导的亚麻(Linum usitatissimum)基因的分离

Isolation of a flax (Linum usitatissimum) gene induced during susceptible infection by flax rust (Melampsora lini).

作者信息

Roberts J K, Pryor A

机构信息

Cooperative Research Centre for Plant Science, Canberra, A.C.T.

出版信息

Plant J. 1995 Jul;8(1):1-8. doi: 10.1046/j.1365-313x.1995.08010001.x.

Abstract

In a susceptible infection of flax (Linum usitatissimum), the obligate rust pathogen (Melampsora lini) can grow in the leaf without triggering the hypersensitive resistance response. The rust establishes specialized structures (haustoria) in plant mesophyll cells and induces changes in plant subcellular organization. Subtraction hybridization methods were used to isolate cDNA clones of mRNAs that have altered expression in infected leaves. Most of the cDNAs recovered were of fungal origin, but one clone, pFIS 1 (flax inducible sequence No. 1), recovered from several independent experiments, was a plant-specified mRNA that showed a 10-fold increase in steady-state levels during susceptible growth. The increase in fis 1 mRNA levels was not seen in the resistant reaction (hypersensitive reaction) and the predicted protein sequence (551 amino acids with a predicted molecular weight of 61 kDa) has no similarity to known pathogenesis-related proteins. Searches of sequence data bases showed that fis 1 encodes a protein which contains amino acid sequence motifs that are conserved in all previously characterized aldehyde dehydrogenases.

摘要

在亚麻(Linum usitatissimum)的易感性感染中,专性锈菌病原体(亚麻栅锈菌Melampsora lini)可在叶片中生长而不引发超敏抗性反应。锈菌在植物叶肉细胞中形成特殊结构(吸器),并诱导植物亚细胞组织发生变化。采用消减杂交方法分离在受感染叶片中表达发生改变的mRNA的cDNA克隆。回收的大多数cDNA来源于真菌,但从几个独立实验中回收的一个克隆pFIS 1(亚麻诱导序列1号)是一种植物特有的mRNA,在易感性生长期间其稳态水平增加了10倍。在抗性反应(超敏反应)中未观察到fis 1 mRNA水平的增加,并且预测的蛋白质序列(551个氨基酸,预测分子量为61 kDa)与已知的病程相关蛋白没有相似性。序列数据库搜索表明,fis 1编码一种蛋白质,该蛋白质包含在所有先前鉴定的醛脱氢酶中保守的氨基酸序列基序。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验