Petranović M, Petranović D, Dohet C, Brooks P, Radman M
Institut Jacques Monod, Paris, France.
Nucleic Acids Res. 1990 Apr 25;18(8):2159-62. doi: 10.1093/nar/18.8.2159.
DNAs from phage mutants M13mp18 and M13mp18/MP-1 were used to construct two closed circular heteroduplexes. One of them carried the sequence 5'-CCTGGG-3' 3'-GGGCCC-5' with a T.G mismatch at the position 6248. The other carried the sequence 5'-CCCGGG-3' 3'-GGACCC-5' with a C.A mismatch at the same position. Heteroduplexes were exposed to 7 restriction endonucleases having recognition sites within the sequence 5'-CCCGGG-3' 3'-GGGCCC-5' and to 1 restriction endonuclease having a recognition site within the sequence 5'-CCTGGG-3' 3'-GGACCC-5'. All tested enzymes cleaved at least one mismatch-containing sequence although with reduced efficiency. Smal and Xmal tolerated both mismatch-containing sequences. Aval, Hpall, Mspl, Ncil and Nsplll were able to tolerate only the T.G containing sequence, while BstNl was able to tolerate only the C.A containing sequence. It is inferred that the tolerance displayed by Smal and Xmal depends on the presence of either the original purines or the original pyrimidines in mismatches of both the T.G and C.A type and that all other tested enzymes require the presence of the original purines in mismaches of both types.
噬菌体突变体M13mp18和M13mp18/MP - 1的DNA被用于构建两个闭环异源双链体。其中一个携带序列5'-CCTGGG-3' 3'-GGGCCC-5',在位置6248处存在T.G错配。另一个携带序列5'-CCCGGG-3' 3'-GGACCC-5',在相同位置存在C.A错配。异源双链体分别用7种在序列5'-CCCGGG-3' 3'-GGGCCC-5'内有识别位点的限制性内切酶以及1种在序列5'-CCTGGG-3' 3'-GGACCC-5'内有识别位点的限制性内切酶进行处理。所有测试的酶都至少切割了一个含错配的序列,尽管效率有所降低。Smal和Xmal能耐受两个含错配的序列。Aval、Hpall、Mspl、Ncil和Nsplll只能耐受含T.G的序列,而BstNl只能耐受含C.A的序列。由此推断,Smal和Xmal表现出的耐受性取决于T.G和C.A两种类型错配中原始嘌呤或原始嘧啶的存在,而所有其他测试的酶在两种类型的错配中都需要原始嘌呤的存在。