Suppr超能文献

利用荧光核糖核酸酶保护(FRIP)分析法对日本水稻(Oryza sativa L.)DNA中的单核苷酸多态性(SNP)进行品种鉴别。

Fluorogenic ribonuclease protection (FRIP) analysis of single nucleotide polymorphisms (SNPs) in Japanese Rice (Oryza sativa L.) DNA for cultivar discrimination.

作者信息

Kitaoka Momoko, Wada Takuya, Nishio Takeshi, Goto Masahiro

机构信息

Department of Applied Chemistry, Graduate School of Engineering, Kyushu University, Fukuoka, Japan.

出版信息

Biosci Biotechnol Biochem. 2010;74(11):2189-93. doi: 10.1271/bbb.100351. Epub 2010 Nov 7.

Abstract

A rapid and easy method to discriminate plant cultivars is indispensable to confirm food labeling. We established a fluorogenic ribonuclease protection (FRIP) assay to discriminate Japanese rice (Oryza sativa L.) cultivars based on single nucleotide polymorphisms (SNPs). The FRIP assay uses a hybridization technique between fluorescent probes and the target sequence prepared by run-off transcription, but the requirement of two PCR thermocycles is the problem when preparing template DNA for run-off transcription from rice genomic DNA. In this study, we designed new PCR primers with asymmetric melting temperatures. These primers amplified the target SNP marker containing a T7 RNA polymerase promoter sequence upstream of the target sequence in a single PCR. Moreover, 100 cultivars were discriminated with the patterns of 15 SNPs. The assay can be used as a rapid method of analysis to discriminate Japanese rice cultivars.

摘要

一种快速简便的鉴别植物品种的方法对于确认食品标签至关重要。我们建立了一种荧光核糖核酸酶保护(FRIP)分析方法,用于基于单核苷酸多态性(SNP)鉴别日本水稻(Oryza sativa L.)品种。FRIP分析使用荧光探针与通过径流转录制备的靶序列之间的杂交技术,但从水稻基因组DNA制备用于径流转录的模板DNA时,需要两个PCR热循环是个问题。在本研究中,我们设计了具有不对称解链温度的新PCR引物。这些引物在单个PCR中扩增了在靶序列上游包含T7 RNA聚合酶启动子序列的靶SNP标记。此外,利用15个SNP的模式鉴别了100个品种。该分析方法可作为一种快速分析方法用于鉴别日本水稻品种。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验