TARGETED GENE WALKING POLYMERASE CHAIN-REACTION

被引:156
作者
PARKER, JD [1 ]
RABINOVITCH, PS [1 ]
BURMER, GC [1 ]
机构
[1] UNIV WASHINGTON,DEPT PATHOL,SEATTLE,WA 98195
关键词
D O I
10.1093/nar/19.11.3055
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We describe a modification of a polymerase chain reaction method called 'targeted gene walking' that can be used for the amplification of unknown DNA sequences adjacent to a short stretch of known sequence by using the combination of a single, targeted sequence specific PCR primer with a second, nonspecific 'walking' primer. This technique can replace conventional cloning and screening methods with a single step PCR protocol to greatly expedite the isolation of sequences either upstream or downstream from a known sequence. A number of potential applications are discussed, including its utility as an alternative to cloning and screening for new genes or cDNAs, as a method for searching for polymorphic sites, restriction endonuclease or regulatory regions, and its adaptation to rapidly sequence DNA of lengthy unknown regions that are contiguous to known genes.
引用
收藏
页码:3055 / 3060
页数:6
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