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基于核糖体蛋白操纵子的聚合酶链反应(PCR)和限制性片段长度多态性(RFLP)分析。

PCR and RFLP analyses based on the ribosomal protein operon.

作者信息

Martini Marta, Lee Ing-Ming

机构信息

Department of Agriculture and Environmental Sciences, University of Udine, Udine, Italy.

出版信息

Methods Mol Biol. 2013;938:173-88. doi: 10.1007/978-1-62703-089-2_15.

Abstract

Differentiation and classification of phytoplasmas have been primarily based on the highly conserved 16S rRNA gene. RFLP analysis of 16S rRNA gene sequences has identified 31 16S rRNA (16Sr) groups and more than 100 16Sr subgroups. Classification of phytoplasma strains can, however, become more refined and specific if moderately conserved genes, such as the ribosomal protein (rp) genes, are used as genetic markers. The use of additional genetic markers enhances the resolving power of phytoplasma classification. This chapter describes the methodology of detection, differentiation, and classification of phytoplasma strains based on rp gene sequences. RFLP analysis of amplicons obtained by group- or subgroup-specific rp gene-based primers is used for finer differentiation of phytoplasma strains within a given group or subgroup. The rp gene-based classification not only readily resolves 16Sr subgroups within a given 16Sr group, but also provides finer differentiation of closely related phytoplasma strains. Many individual 16Sr subgroups can be further differentiated into two or more distinct rp subgroups.

摘要

植原体的分化和分类主要基于高度保守的16S rRNA基因。对16S rRNA基因序列进行限制性片段长度多态性(RFLP)分析已鉴定出31个16S rRNA(16Sr)组和100多个16Sr亚组。然而,如果使用中度保守基因,如核糖体蛋白(rp)基因作为遗传标记,植原体菌株的分类可以变得更加精细和具体。使用额外的遗传标记可提高植原体分类的分辨能力。本章介绍了基于rp基因序列的植原体菌株检测、分化和分类方法。通过基于组或亚组特异性rp基因的引物获得的扩增子进行RFLP分析,用于在给定组或亚组内对植原体菌株进行更精细的分化。基于rp基因的分类不仅能轻松分辨给定16Sr组内的16Sr亚组,还能对密切相关的植原体菌株进行更精细的分化。许多单个的16Sr亚组可进一步分化为两个或更多不同的rp亚组。

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