首页> 外国专利> DNA extension and analysis with rolling primers

DNA extension and analysis with rolling primers

机译:DNA延伸和滚动引物分析

摘要

A novel "primer walking" method for DNA sequencing is provided that comprises repeated cycles nucleotide identification by selective extension and primer advancement along a template by template mutation. An important feature of the invention is providing a set of primers, referred to herein as "rolling primers" that contain complexity-reducing nucleotides for reducing the number of primers required for annealing to every possible primer binding site on a sequencing template. Another important feature of the invention is the systematic replacement of at least one of the four nucleotides in the target polynucleotide with its cognate complexity-reducing nucleotide or complement thereof. Sequencing is initiated by annealing rolling primers differing only in their terminal nucleotides to a primer binding site of a sequencing template so that only the rolling primer whose terminal nucleotide forms a perfect complement with the template leads to the formation of an extension product. After amplifying the double stranded extension product to form an amplicon, the terminal nucleotide, and hence its complement in the template, is identified by the identity of the amplicon. The primer binding site of the template of the successfully amplified polynucleotide is then mutated by, for example, oligonucleotide-directed mutagenesis so that a subsequent rolling primer may be selected from the set that forms a perfectly matched duplex with the mutated template at a site which is shifted towards the direction of extension by one nucleotide relative to the binding site of the previous rolling primer. The steps of selective extension, amplification and identification are then repeated. In this manner, the primers "roll" along the polynucleotide during the sequencing process, moving a base at a time along the template with each cycle.
机译:提供了一种用于DNA测序的新颖的“引物行走”方法,该方法包括通过选择性延伸和通过模板突变沿着模板沿引物进行重复循环来鉴定核苷酸。本发明的重要特征是提供一组引物,在本文中称为“滚动引物”,其包含降低复杂性的核苷酸,用于减少退火至测序模板上每个可能的引物结合位点所需的引物数量。本发明的另一个重要特征是用靶标多核苷酸的降低同源性的核苷酸或其互补序列系统性地替换靶多核苷酸中的四个核苷酸中的至少一个。通过使仅在其末端核苷酸上不同的滚动引物与测序模板的引物结合位点退火来启动测序,从而仅其末端核苷酸与模板形成完美互补的滚动引物导致延伸产物的形成。在扩增双链延伸产物以形成扩增子之后,通过扩增子的身份来鉴定末端核苷酸以及因此其在模板中的互补物。然后,通过例如寡核苷酸定向诱变使成功扩增的多核苷酸的模板的引物结合位点发生突变,从而可以从与该突变的模板形成与该模板完全匹配的双链体的组中选择随后的滚动引物。相对于先前的滚动引物的结合位点,Δα向着延伸方向移动了一个核苷酸。然后重复选择性延伸,扩增和鉴定的步骤。以这种方式,引物在测序过程中沿着多核苷酸“滚动”,在每个循环中一次沿模板移动碱基。

著录项

  • 公开/公告号US5962228A

    专利类型

  • 公开/公告日1999-10-05

    原文格式PDF

  • 申请/专利权人 LYNX THERAPEUTICS INC.;

    申请/专利号US19970916120

  • 发明设计人 SYDNEY BRENNER;

    申请日1997-08-22

  • 分类号C12Q1/68;C07H21/02;C07H21/04;C12N15/00;

  • 国家 US

  • 入库时间 2022-08-22 02:07:07

相似文献

  • 专利
  • 外文文献
  • 中文文献
获取专利

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号