Kitaoka Momoko, Wada Takuya, Nishio Takeshi, Goto Masahiro
Department of Applied Chemistry, Graduate School of Engineering, Kyushu University, Fukuoka, Japan.
Biosci Biotechnol Biochem. 2010;74(11):2189-93. doi: 10.1271/bbb.100351. Epub 2010 Nov 7.
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.
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。