Mathieu Jacques, Alvarez Emilia, Alvarez Pedro J J
Department of Civil and Environmental Engineering, Rice University, Houston, TX, United States.
MethodsX. 2014 May 20;1:23-9. doi: 10.1016/j.mex.2014.05.001. eCollection 2014.
No molecular cloning technique is considered universally reliable, and many suffer from being too laborious, complex, or expensive. Restriction-free cloning is among the simplest, most rapid, and cost-effective methods, but does not always provide successful results. We modified this method to enhance its success rate through the use of exponential amplification coupled with homologous end-joining. This new method, recombination-assisted megaprimer (RAM) cloning, significantly extends the application of restriction-free cloning, and allows efficient vector construction with much less time and effort when restriction-free cloning fails to provide satisfactory results. The following modifications were made to the protocol:•Limited number of PCR cycles for both megaprimer synthesis and the cloning reaction to reduce error propagation.•Elimination of phosphorylation and ligation steps previously reported for cloning methods that used exponential amplification, through the inclusion of a reverse primer in the cloning reaction with a 20 base pair region of homology to the forward primer.•The inclusion of 1 M betaine to enhance both reaction specificity and yield.
没有一种分子克隆技术被认为是普遍可靠的,许多技术存在操作繁琐、过程复杂或成本高昂的问题。无限制克隆是最简单、最快速且最具成本效益的方法之一,但并非总能获得成功的结果。我们对该方法进行了改进,通过结合指数扩增和同源末端连接来提高其成功率。这种新方法,即重组辅助大引物(RAM)克隆,显著扩展了无限制克隆的应用范围,并且在无限制克隆无法提供满意结果时,能够以更少的时间和精力高效构建载体。对实验方案进行了以下修改:
大引物合成和克隆反应的PCR循环次数有限,以减少错误传播。
通过在克隆反应中加入与正向引物具有20个碱基对同源区域的反向引物,省去了先前报道的使用指数扩增的克隆方法中的磷酸化和连接步骤。
加入1 M甜菜碱以提高反应特异性和产量。