Warrens A N, Jones M D, Lechler R I
Department of Immunology, Royal Postgraduate Medical School, Hammersmith Hospital, London, UK.
Gene. 1997 Feb 20;186(1):29-35. doi: 10.1016/s0378-1119(96)00674-9.
Major histocompatibility complex (MHC) proteins play a central role in the immune recognition of antigen. The generation of hybrid MHC molecules has been of great value in elucidating the structure: function relationships of these key glycoproteins. In this report, the generation of cDNAs coding for seven such hybrid proteins is described. We have used the technique of splicing by overlap extension by the polymerase chain reaction (SOE by PCR) [Horton, R.M., Hunt, H.D., Ho, S.N., Pullen, J.K. and Pease, L.R. (1989) Engineering hybrid genes without the use of restriction enzymes: gene splicing by overlap extension. Gene 77, 61-68] to generate intermediate products of each of the components of the hybrid, tipped with a small sequence of the other, and then mixed these products in a second-stage PCR to produce the final spliced product. Where we were unable to generate final product, we introduced an additional step of asymmetric PCR synthesis to generate an excess of those strands which would anneal in the final PCR and found this to be effective. We noted a significant but manageable mutation rate, possibly contributed to by the tendency of DNA polymerase to add additional non-templated nucleotides [Hu, G. (1993) DNA polymerase-catalyzed addition of nontemplated extra nucleotides to the 3' end of a DNA fragment. DNA Cell Biol. 12, 763-770]. To avoid this, we modified our protocol to include a stage of blunting our intermediate products with T4 DNA polymerase prior to mixing them in the final PCR. We present this system as an effective mechanism to splice DNA.
主要组织相容性复合体(MHC)蛋白在抗原的免疫识别中起核心作用。杂合MHC分子的产生对于阐明这些关键糖蛋白的结构与功能关系具有重要价值。在本报告中,描述了编码七种此类杂合蛋白的cDNA的产生。我们使用了聚合酶链反应重叠延伸剪接技术(PCR介导的SOE)[霍顿,R.M.,亨特,H.D.,何,S.N.,普伦,J.K.和皮斯,L.R.(1989年)无需使用限制酶构建杂合基因:重叠延伸剪接。基因77,61 - 68]来生成杂合子各组分的中间产物,每个中间产物都带有另一组分的一小段序列,然后在第二阶段PCR中将这些产物混合以产生最终的剪接产物。当我们无法生成最终产物时,我们引入了一个额外的不对称PCR合成步骤,以产生过量的那些在最终PCR中会退火的链,结果发现这是有效的。我们注意到存在显著但可控的突变率,这可能是由于DNA聚合酶倾向于添加额外的非模板核苷酸所致[胡,G.(1993年)DNA聚合酶催化在DNA片段3'端添加非模板额外核苷酸。DNA细胞生物学。12,763 - 770]。为避免这种情况,我们修改了方案,在最终PCR混合之前,增加了一个用T4 DNA聚合酶使中间产物平端化的步骤。我们将此系统作为一种有效的DNA剪接机制进行展示。