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Conservation of motifs within the unusually variable polypeptide sequences of type I restriction and modification enzymes
Authors:Noreen E Murray  Anne S Daniel  Gill M Cowan  Paul M Sharp
Institution:Institute of Cell and Molecular Biology, University of Edinburgh, Edinburgh EH9 3JR, UK.;The Rowett Research Institute, Aberdeen AB2 9SB, UK.;Institute of Molecular Medicine, Oxford 0X3 9DU, UK.;Department of Genetics, Trinity College, Dublin 2, Ireland.
Abstract:Type I restriction enzymes comprise three subunits encoded by genes designated hsdR, hsdM, and hsdS; S confers sequence specificity. Three families of enzymes are known and within families, but not between, hsdM and hsdR are conserved. Consequently, interfamily comparisons of M and R sequences focus on regions of putative functional significance, while both inter- and intrafamily comparisons address the origin, nature and role of diversity of type I restriction systems. We have determined the sequence of the hsdR gene for EcoA, thus making available sequences of all three hsd genes of one representative from each family. The predicted R polypeptide sequences share conserved regions with one superfamily of putative helicases, so-called ‘DEAD box’ proteins; these conserved sequences may be associated with the ATP-dependent translocation of DNA that precedes restriction. We also present hsdM and hsdR sequences for EcoE, a member of the same family as EcoA. The sequences of the M and R genes of EcoA and EcoE are at least as divergent as typical genes from Escherichia coli and Salmonella, perhaps as the result of selection favouring diversity of restriction specificities combined with lateral transfer among different species.
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