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pubmed-article:2159641pubmed:abstractTextDNAs 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.lld:pubmed
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pubmed-article:2159641pubmed:dateRevised2009-11-18lld:pubmed
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pubmed-article:2159641pubmed:articleTitleSome restriction endonucleases tolerate single mismatches of the pyrimidine.purine type.lld:pubmed
pubmed-article:2159641pubmed:affiliationInstitut Jacques Monod, Paris, France.lld:pubmed
pubmed-article:2159641pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:2159641pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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