Type III restriction enzymes need two inversely oriented recognition sites for DNA cleavage
- 30 January 1992
- journal article
- research article
- Published by Springer Nature in Nature
- Vol. 355 (6359) , 467-469
- https://doi.org/10.1038/355467a0
Abstract
TYPE III restriction/modification enzymes recognize short, non-palindromic sequences that can be methylated on only one strand, with the paradoxical consequence that during replication of what is in effect hemimethylated DNA totally unmodified sites arise1. Why the unmodified sites are not subject to suicidal restriction was not clear. Here we show that restriction requires two unmodified recognition sites that can be separated by different distances but which must be in inverse orientation. All of the unmodified sites in newly replicated DNA are of course in the same orientation, which explains why they are not restricted. This result may be of relevance to other manifestations of anisotropy in double-stranded DNA, such as genetic imprinting2.Keywords
This publication has 9 references indexed in Scilit:
- M.EcoPl5 methylates the second adenine in its recognition sequenceNucleic Acids Research, 1991
- Effect of manganese ions on the incorporation of dideoxynucleotides by bacteriophage T7 DNA polymerase and Escherichia coli DNA polymerase I.Proceedings of the National Academy of Sciences, 1989
- A simple and rapid method for the selection of oligodeoxynucleotide-directed mutantsGene, 1988
- Differentiated parental DNA strands confer developmental asymmetry on daughter cells in fission yeastNature, 1987
- Unusual occurrence of EcoP1 and EcoP15 recognition sites and counterselection of type II methylation and restriction sequences in bacteriophage T7 DNAGene, 1986
- DNA restriction-modification enzymes of phage P1 and plasmid p15BJournal of Molecular Biology, 1983
- Nucleotide sequence of the filamentous bacteriophage M13 DNA genome: comparison with phage fdGene, 1980
- DNA recognition and cleavage by the EcoP15 restriction endonucleaseJournal of Molecular Biology, 1979
- Purification and properties of the P15 specific restriction endonuclease from Escherichia coli.Journal of Biological Chemistry, 1977