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卵菌病原体致病疫霉的转化

Transformation of the oomycete pathogen, Phytophthora infestans.

作者信息

Judelson H S, Tyler B M, Michelmore R W

机构信息

Department of Vegetable Crops, University of California, Davis 95616.

出版信息

Mol Plant Microbe Interact. 1991 Nov-Dec;4(6):602-7. doi: 10.1094/mpmi-4-602.

Abstract

A stable transformation procedure has been developed for Phytophthora infestans, an oomycete fungus that causes the late blight diseases of potato and tomato. This is the first description of reliable methods for transformation in an oomycete pathogen. Drug-resistant transformants were obtained by using vectors that contained bacterial genes for resistance to hygromycin B or G418 fused to promoters and terminators from the Hsp70 and Ham34 genes of the oomycete, Bremia lactucae. Using polyethylene glycol and CaCl2, vector DNA was introduced into protoplasts as a complex with cationic liposomes or with carrier DNA only. Transformants were obtained at similar frequencies with each combination of promoter and selectable marker and were confirmed by DNA and RNA hybridization and phosphotransferase assays. Transformation occurred through the integration of single or tandemly repeated copies of the plasmids into genomic DNA, conferring mitotically stable drug-resistant phenotypes. The sizes of the marker gene mRNAs in each transformant and the results of transcript mapping studies were consistent with the function of the B. lactucae regulatory sequences in P. infestans. A hygromycin-resistant transformant was tested and found to maintain pathogenicity, indicating that the gene transfer procedure will be useful for the molecular analysis of genes relevant to disease.

摘要

已为致病疫霉开发出一种稳定的转化程序,致病疫霉是一种卵菌纲真菌,可引发马铃薯和番茄的晚疫病。这是首次描述卵菌病原体中可靠的转化方法。通过使用含有对潮霉素B或G418具有抗性的细菌基因的载体获得了抗药转化体,这些基因与来自卵菌莴苣盘梗霉的Hsp70和Ham34基因的启动子和终止子融合。使用聚乙二醇和氯化钙,载体DNA作为与阳离子脂质体或仅与载体DNA的复合物被引入原生质体。每种启动子和选择标记的组合都以相似的频率获得了转化体,并通过DNA和RNA杂交以及磷酸转移酶测定进行了确认。转化是通过质粒的单拷贝或串联重复拷贝整合到基因组DNA中发生的,赋予了有丝分裂稳定的抗药表型。每个转化体中标记基因mRNA的大小以及转录图谱研究的结果与致病疫霉中莴苣盘梗霉调控序列的功能一致。对一个潮霉素抗性转化体进行了测试,发现其保持致病性,这表明该基因转移程序将有助于对与疾病相关的基因进行分子分析。

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