Method for fragmenting DNA by nick translation
Providing herein, among other things, are kits, compositions and methods that relate to DNA fragmentation. An embodiment of a composition provides combining: one or more enzymes capable of nick translating activity, a dNTP mix comprising at least one dNTP having a modified base, and at least one modification-sensitive nicking endonuclease that is prevented from nicking DNA if its recognition site contains the modified base. When the composition is added to a sample comprising a double-stranded DNA template that comprises recognition sites for the modification-sensitive nicking endonuclease, a reaction mix was produced which could be incubated for any time period in excess of about 5 minutes to produce fragments of a desired size of the double-stranded DNA template. In this method, the fragments produced include the modified base and, as such, are not re-nicked by the nicking endonuclease.
1. A method for generating fragments of DNA of a predetermined size from a genomic DNA, comprising:
(a) nicking DNA with a modification sensitive nicking endonuclease or homodimer restriction endonuclease and permitting nick translation with a strand displacing DNA polymerase;
(b) permitting the DNA polymerase to move the nick on one strand of the DNA until the polymerase meets a nick on the second strand;
(c) preventing secondary nicks at a single site by means of modified nucleotides introduced into the nick site;
(d) generating fragments having a desired length selected from a size range of 50 bp-50 kb.
2. The method according to claim 1 , wherein the homodimer restriction endonuclease is selected from the group consisting of NciI, AsuC21, BcnI and BpuMI and isoschizomers thereof.
3. The method according to claim 1 , wherein the nicking endonuclease is Nt.CviPII.
4. The method according to claim 1 , wherein (c) comprises selecting a ratio of nicking endonuclease to polymerase in the range of 1:50-1:5000 (units:units).