Lapeyre B, Amalric F
Gene. 1985;37(1-3):215-20. doi: 10.1016/0378-1119(85)90275-6.
An easy and quick method to synthesize large cDNA molecules and to clone them with very high efficiency in the expression vector lambda gt11 is described. The technique employs RNase H and Escherichia coli DNA ligase treatment during second-strand synthesis, followed by repair of the ds cDNA extremities by S1 nuclease and PolIk (Klenow fragment) treatment. This treatment allows efficient addition of suitable linkers and results in a 100-fold increase in the yield of cloned cDNA, when compared with other published techniques. Using 75 ng of poly(A)+ RNA from CHO cells, we have prepared a library of 1.1 X 10(7) clones. This library was screened with polyclonal antibodies raised against a 100-kDal nucleolar protein of CHO cells. Five recombinants were isolated with inserts of 500-2500 bp. The average size of cDNA obtained by this method is considerable: the 2500-bp cDNA represents 90% of the mRNA coding for the 100-kDal protein.
本文描述了一种简便快速的方法,可用于合成大的cDNA分子,并以非常高的效率将其克隆到表达载体λgt11中。该技术在第二链合成过程中采用核糖核酸酶H和大肠杆菌DNA连接酶处理,随后通过S1核酸酶和PolIk(克列诺片段)处理修复双链cDNA末端。与其他已发表的技术相比,这种处理能够高效添加合适的接头,并使克隆cDNA的产量提高100倍。使用来自CHO细胞的75 ng聚腺苷酸加尾RNA,我们构建了一个包含1.1×10⁷个克隆的文库。用针对CHO细胞100-kDal核仁蛋白产生的多克隆抗体对该文库进行筛选。分离出了五个重组体,其插入片段大小为500 - 2500 bp。通过该方法获得的cDNA平均大小可观:2500-bp的cDNA占编码100-kDal蛋白的mRNA的90%。