5′ end cDNA amplification using classic RACE

被引:187
作者
Scotto-Lavino, Elizabeth
Du, Guangwei
Frohman, Michael A. [1 ]
机构
[1] SUNY Stony Brook, Grad Program Mol & Cellular Pharmacol, Stony Brook, NY 11794 USA
[2] SUNY Stony Brook, Dept Pharmacol Sci, Stony Brook, NY 11794 USA
[3] SUNY Stony Brook, Ctr Dev Genet, Stony Brook, NY 11794 USA
关键词
D O I
10.1038/nprot.2006.480
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The 5' ends of transcripts provide important information about transcription initiation sites and the approximate locations of local cis-acting enhancer elements; it is therefore important to establish the 5' ends with some precision. RACE (rapid amplification of cDNA ends) PCR is useful for quickly obtaining full length cDNAs for mRNAs for which only part of the sequence is known and to identify alternative 5' or 3' ends of fully sequenced genes. The method consists of using PCR to amplify, from complex mixtures of cellular mRNA, the regions between the known parts of the sequence and non-specific tags appended to the ends of the cDNA. Whereas the poly(A) tail serves to provide such a tag at the 3' end of the mRNA, an artificial one needs to be generated at the 5' end, and various approaches have been described to address this step. The classical scheme for 5' RACE described here is simple, suffices in many instances in which RACE is needed and can be performed in 1-3 days.
引用
收藏
页码:2555 / 2562
页数:8
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