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使用含噁唑啉的连接片段的 T4 DNA 连接酶单核苷酸多态性分析中对鸟嘌呤:胞嘧啶的准确区分。

Accurate guanine:cytosine discrimination in T4 DNA ligase-based single nucleotide polymorphism analysis using an oxanine-containing ligation fragment.

机构信息

Department of Biotechnology and Bioinformatics, Korea University, Jochiwon, Chungnam, Republic of Korea.

出版信息

Anal Biochem. 2010 Mar 15;398(2):257-9. doi: 10.1016/j.ab.2009.11.014. Epub 2009 Nov 14.

Abstract

T4 DNA ligase-based mismatch detection methods have been proposed as useful strategies for single nucleotide polymorphism (SNP) analyses. However, there is a critical problem for cytosine/thymine (C/T) SNP analyses: guanine:thymine (G:T) mismatch is not distinguished from guanine:cytosine (G:C). Here we employed chemically modified nucleobases, such as oxanine and hypoxanthine, at the end of a ligation fragment and analyzed their influence on the ligation efficiency between G:C and G:T. Successful ligation for G:C and no ligation for G:T were observed when oxanine was employed adjacent to guanine in the ligation junction. This ligation method using an oxanine-containing fragment has strong potentials for the accurate analysis of C/T SNPs.

摘要

基于 T4 DNA 连接酶的错配检测方法已被提议作为单核苷酸多态性 (SNP) 分析的有用策略。然而,对于胞嘧啶/胸腺嘧啶 (C/T) SNP 分析存在一个关键问题:鸟嘌呤:胸腺嘧啶 (G:T) 错配不能与鸟嘌呤:胞嘧啶 (G:C) 区分。在这里,我们在连接片段的末端使用了化学修饰的碱基,如噁嗪和次黄嘌呤,并分析了它们对 G:C 和 G:T 之间连接效率的影响。当噁嗪在连接接头中紧邻鸟嘌呤时,观察到 G:C 的成功连接和 G:T 的无连接。这种使用含噁嗪片段的连接方法对于 C/T SNP 的准确分析具有很强的潜力。

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