单引物位点特异性嵌套 PCR,用于准确快速地进行基因组漫步。

IF 1.7 4区 生物学 Q4 BIOCHEMICAL RESEARCH METHODS Journal of microbiological methods Pub Date : 2024-03-28 DOI:10.1016/j.mimet.2024.106926
Xinyue Guo , Yisong Zhu , Zhenkang Pan , Hao Pan , Haixing Li
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引用次数: 0

摘要

基因组漫步是一种用于揭示已知DNA侧翼未表征DNA区域的分子工具,已被广泛应用于生物科学及相关领域。本研究开发了一种可靠、高效的基于 PCR 的基因组漫步方法,命名为单引物位点特异性嵌套 PCR(SPN-PCR)。一套 SPN-PCR 序列由三个单引物嵌套 PCR 扩增组成。初级宽松热循环促使最外层的嵌套位点特异性引物(NSSP)与 DNA 模板上的多个位点部分结合,合成多条单链 DNA(ssDNA)。其中,目标 ssDNA 在随后的严格循环中会被成倍扩增,因为其 3' 部分具有最外层 NSSP 的补码;但非目标 ssDNA 则不能被扩增,因为它不具有这种补码。严格的二级和三级 PCR 也会专门富集这种目标 DNA。最后,目标 DNA 产物成为主要产物。通过对两个不同物种的几个选定基因进行基因组漫步,验证了 SPN-PCR 的可行性。
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Single primer site-specific nested PCR for accurate and rapid genome-walking

Genome-walking is a molecular tool used to unveil uncharacterized DNA regions flanking a known DNA, which has been widely used in bioscience and related areas. This study developed a reliable and efficient PCR-based genome-walking approach, named as single primer site-specific nested PCR (SPN-PCR). A SPN-PCR set sequentially consists of three single-primer nested PCR amplifications. The primary relaxed thermal cycle promotes outmost nested site-specific primer (NSSP) to partially combine with numerous places on DNA template, synthesizing many single-stranded DNAs (ssDNA). Among them, the target ssDNA is exponentially amplified in the subsequent stringent cycles, as its 3′ part possesses the outmost NSSP complement; but a non-target ssDNA cannot be amplified, because it does not possess such a complement. Stringent secondary and tertiary PCRs also exclusively enrich this target DNA. Finally, the target DNA product becomes predominant. The feasibility of SPN-PCR was validated by genome-walking several selected genes from two divergent species.

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来源期刊
Journal of microbiological methods
Journal of microbiological methods 生物-生化研究方法
CiteScore
4.30
自引率
4.50%
发文量
151
审稿时长
29 days
期刊介绍: The Journal of Microbiological Methods publishes scholarly and original articles, notes and review articles. These articles must include novel and/or state-of-the-art methods, or significant improvements to existing methods. Novel and innovative applications of current methods that are validated and useful will also be published. JMM strives for scholarship, innovation and excellence. This demands scientific rigour, the best available methods and technologies, correctly replicated experiments/tests, the inclusion of proper controls, calibrations, and the correct statistical analysis. The presentation of the data must support the interpretation of the method/approach. All aspects of microbiology are covered, except virology. These include agricultural microbiology, applied and environmental microbiology, bioassays, bioinformatics, biotechnology, biochemical microbiology, clinical microbiology, diagnostics, food monitoring and quality control microbiology, microbial genetics and genomics, geomicrobiology, microbiome methods regardless of habitat, high through-put sequencing methods and analysis, microbial pathogenesis and host responses, metabolomics, metagenomics, metaproteomics, microbial ecology and diversity, microbial physiology, microbial ultra-structure, microscopic and imaging methods, molecular microbiology, mycology, novel mathematical microbiology and modelling, parasitology, plant-microbe interactions, protein markers/profiles, proteomics, pyrosequencing, public health microbiology, radioisotopes applied to microbiology, robotics applied to microbiological methods,rumen microbiology, microbiological methods for space missions and extreme environments, sampling methods and samplers, soil and sediment microbiology, transcriptomics, veterinary microbiology, sero-diagnostics and typing/identification.
期刊最新文献
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