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[用于检测人类基因组变异的温度调制高效液相色谱法]

[Temperature-modulated high-performance liquid chromatography for detecting variation in human genome].

作者信息

Hou Y, Zhang S

出版信息

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2000 Jun;17(3):145-8.

Abstract

Recently, temperature modulated heteroduplex analysis (TMHA) based upon ion-pair reversed-phase high-performance liquid chromatography has been developed as a tool for polymorphisms and novel mutation detection in human genome. This new approach, with increased accuracy and throughput over traditional methods. This new approach is also known as denaturing high performance liquid chromatography(DHPLC). However, the terms of both TMHA and DHPLC should be considered carefully. Firstly, it is DNA molecular that is denatured in high performance liquid chromatography but not the method or the instrument. Secondly, the temperature in the liquid chromatograph is modulated according to Tm (melting temperature) of the DNA fragments. As it is known, Tm is the temperature at which a population of double-stranded nucleic acid molecules becomes half-dissociated into single strands, and under this temperature, half of the DNA molecules is still not denaturing. Thirdly, the targets for detection are both the homoduplexes and the mismatched heteroduplexes, which are double-stranded nucleic acid molecules and are annealing. The term of DHPLC may lead to confusion in annealing and denaturing. In addition, since TMHA can be carried out using gel electrophoresis and HPLC, there is a need to distinguish HPLC from gel electrophoresis. Therefore, we suggest a new term for this technology, which is TmHPLC (temperature-modulated high- performance liquid chromatography). This term not only provides a clear definition for this new method, but also includes both TMHA and HPLC. More importantly, TmHPLC implies that the temperature in HPLC is modulated according to Tm of the DNA fragments. We also review advances in detecting variation through TmHPLC. This new approach leads to significant reduction of sequencing efforts for searching novel mutations and polymorphisms, and because of its high sample throughput, to faster data generation. This implies that TmHPLC is a sensitive, accurate, and cost effective approach to screening sequence variation in human genome.

摘要

最近,基于离子对反相高效液相色谱的温度调制异源双链分析(TMHA)已被开发出来,作为检测人类基因组多态性和新突变的一种工具。这种新方法比传统方法具有更高的准确性和通量。这种新方法也被称为变性高效液相色谱(DHPLC)。然而,对于TMHA和DHPLC这两个术语都应仔细考量。首先,在高效液相色谱中变性的是DNA分子,而非方法或仪器。其次,液相色谱中的温度是根据DNA片段的解链温度(Tm)进行调制的。众所周知,Tm是双链核酸分子群体变为半解离成单链的温度,在此温度下,仍有一半的DNA分子未变性。第三,检测的目标既有同源双链,也有不匹配的异源双链,它们都是双链核酸分子且正在退火。DHPLC这个术语可能会在退火和变性方面导致混淆。此外,由于TMHA可以使用凝胶电泳和HPLC来进行,所以有必要将HPLC与凝胶电泳区分开来。因此,我们建议为这项技术采用一个新术语,即TmHPLC(温度调制高效液相色谱)。这个术语不仅为这种新方法提供了清晰的定义,还涵盖了TMHA和HPLC。更重要的是,TmHPLC意味着HPLC中的温度是根据DNA片段的Tm进行调制的。我们还回顾了通过TmHPLC检测变异的进展。这种新方法显著减少了搜索新突变和多态性时的测序工作量,并且由于其高样本通量,能够更快地生成数据。这意味着TmHPLC是一种用于筛选人类基因组序列变异的灵敏、准确且经济高效的方法。

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