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改良等位基因特异性 qPCR (ASQ) 基因分型。

Modified Allele-Specific qPCR (ASQ) Genotyping.

机构信息

Kazakh Research Institute of Agriculture and Plant Growing, Almalybak, Almaty, Kazakhstan.

S.Seifullin Kazakh AgroTechnical University, Astana, Kazakhstan.

出版信息

Methods Mol Biol. 2023;2638:231-247. doi: 10.1007/978-1-0716-3024-2_16.

Abstract

The allele-specific qPCR (ASQ) method for SNP (single nucleotide polymorphism) detection is based on the FRET (fluorescence resonance energy transfer) system, a system using position-dependent fluorescent dyes and quenches. The modified ASQ method requires two separate components: (1) the allele-specific part, two AS primers targeting the SNP with identity in the penultimate positions at the 3'-end and specific tags in the 5'-end, and (2) the universal part, two universal probes (UPs) with corresponding tags and different fluorescent dyes in the 5'-end and a single common universal probe with a quencher in the 3'-ends (Uni-Q), complementary to all UP tags. There are two major variations of the ASQ method, with either short 4-bp tags (variant A) or longer 6-bp tags (variant B), both of which have been successfully used for SNP genotyping in plants. The modified ASQ method is much cheaper compared to other similar FRET-based methods because the most expensive parts, the universal probes, have a short and linear structure, where fluorophores and quenchers are located in the ends but not incorporated inside of the sequences.

摘要

等位基因特异性 qPCR (ASQ) 方法用于 SNP(单核苷酸多态性)检测,基于 FRET(荧光共振能量转移)系统,该系统使用位置依赖的荧光染料和猝灭剂。改良的 ASQ 方法需要两个单独的组件:(1)等位基因特异性部分,两个 AS 引物针对 SNP,在 3'-末端的倒数第二个位置具有相同的碱基,在 5'-末端具有特异性标签,以及(2)通用部分,两个通用探针 (UP) 在 5'-末端具有相应的标签和不同的荧光染料,以及一个带有 3'-末端猝灭剂的单个通用探针(Uni-Q),与所有 UP 标签互补。ASQ 方法有两种主要变体,分别使用 4 个碱基短标签(变体 A)或 6 个碱基长标签(变体 B),这两种变体都已成功用于植物中的 SNP 基因分型。与其他基于 FRET 的类似方法相比,改良的 ASQ 方法要便宜得多,因为最昂贵的部分,通用探针,具有短而线性的结构,荧光团和猝灭剂位于末端而不是序列内部。

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