利用核酸酶S1进行基因组DNA位点选择性切割的人工限制性DNA切割器

Q4 Chemistry
Arivazhagan Rajendran, Narumi Shigi, Jun Sumaoka, Makoto Komiyama
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引用次数: 1

摘要

通过将一对伪互补肽核酸(pcPNAs)与S1核酸酶结合,可以获得一种在预定位点切割DNA的新工具。互补的pcpna侵入DNA双链和碱基对到目标位点的每条链上,形成单链区域,被S1核酸酶切割。通过pcpna的设计,可以自由调节裂解位点。这种方法可用于切割人类基因组中的单个位点。该协议提出了使用这个多功能新工具的选择性切割的实验细节。©2019 by John Wiley &儿子,Inc。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Artificial Restriction DNA Cutter Using Nuclease S1 for Site-Selective Scission of Genomic DNA

By combining a pair of pseudo-complementary peptide nucleic acids (pcPNAs) with S1 nuclease, a novel tool to cut DNA at a predetermined site can be obtained. Complementary pcPNAs invade the DNA duplex and base pair to each strand of a target site, creating single-stranded regions that are cleaved by S1 nuclease. The scission site can be freely modulated by the design of pcPNAs. This method can be used to cleave a single site in the human genome. This protocol presents experimental details for site-selective scission using this versatile new tool. © 2019 by John Wiley & Sons, Inc.

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来源期刊
Current Protocols in Nucleic Acid Chemistry
Current Protocols in Nucleic Acid Chemistry Chemistry-Organic Chemistry
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期刊介绍: Published in association with International Society for Nucleosides, Nucleotides & Nucleic Acids (IS3NA) , Current Protocols in Nucleic Acid Chemistry is equally valuable for biotech, pharmaceutical, and academic labs. It is the resource for designing and running successful research projects in the rapidly growing and changing field of nucleic acid, nucleotide, and nucleoside research.
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