Kang Dong-chul, Fisher Paul B
Hallym University, Ilsong Institute of Life Science, Anyang, Kyeonggi-do, Republic of Korea.
Methods Mol Biol. 2007;383:123-33. doi: 10.1007/978-1-59745-335-6_8.
Several approaches, generally referred to as rapid amplification of cDNA ends, are currently used as a means of obtaining full-length cDNA clones by PCR. However, these protocols are not infallible and in specific instances they have proven unsuccessful, emphasizing a need for further refinement. A novel method, the complete open reading frame (C-ORF) technique, is presently described, which has proven successful in cases, where standard rapid amplification of cDNA ends (RACE) has not worked. In C-ORF, the 5' PCR primer site is provided by a degenerative stem-loop annealing primer, which consists of a stem-loop structure and a 3' random 12-mer. degenerative stem-loop annealing primer is designed to anneal at random sites of the first strand cDNA, while promoting second strand synthesis from the end of given cDNA. Although this technique manifests weak sequence preference for GC-rich regions, in practice it has been successfully applied to clone both known and unknown genes with varying regions of GC-rich content. C-ORF does not use additional enzymes other than reverse transcriptase and Taq polymerase making it a cost-effective and relatively simple method that should be of general utility for gene cloning in multiple laboratories.
目前有几种方法,通常称为cDNA末端快速扩增,被用作通过聚合酶链反应(PCR)获得全长cDNA克隆的手段。然而,这些方案并非万无一失,在某些特定情况下已被证明是不成功的,这凸显了进一步改进的必要性。本文介绍了一种新方法,即完整开放阅读框(C-ORF)技术,该技术在标准的cDNA末端快速扩增(RACE)不起作用的情况下已被证明是成功的。在C-ORF中,5' PCR引物位点由一个简并茎环退火引物提供,该引物由一个茎环结构和一个3' 随机12聚体组成。简并茎环退火引物设计用于在第一链cDNA的随机位点退火,同时促进从给定cDNA末端开始的第二链合成。尽管该技术对富含GC的区域表现出较弱的序列偏好,但在实践中它已成功应用于克隆具有不同富含GC含量区域的已知和未知基因。C-ORF除了逆转录酶和Taq聚合酶外不使用其他额外的酶,这使其成为一种经济高效且相对简单的方法,应该对多个实验室的基因克隆具有普遍实用性。