Method for ligating nucleic acids and molecular cloning
View Patent ↗The invention provides methods of covalently joining nucleic acid molecules and methods of molecular cloning. The methods provide either sequential or simultaneous ligation of flanking or vector nucleic acid molecules to nucleic acid insert molecules by topoisomerase and DNA ligase. The methods provide for directional and non-directional covalent joining and cloning of nucleic acid molecules.
1. A method of molecular cloning, wherein a nucleic acid insert molecule is covalently joined to first and second double stranded nucleic acid flanking molecules to form a ligated molecule, the method comprising:
(A) incubating said insert molecule and said flanking molecules, wherein each end of said insert molecule comprises a 5′-hydroxyl group, and wherein one end only of each of said first and second flanking molecules comprises a covalently bound topoisomerase polypeptide, under conditions which permit their covalent joining to form a ligated molecule comprising a said insert molecule positioned between a said first and a said second flanking molecule; and
(B) transforming the covalently joined insert molecule of step (a) into a host cell to obtain transformants.
2. The method of claim 1 , wherein a said first and a said second nucleic acid flanking molecules comprise a left and a right vector arm, respectively, such that a said insert molecule is flanked by a said left vector arm and a said right vector arm.
3. The method of claim 2 , wherein said left and right vector arms each comprise a free end that is not joined to an insert molecule, said method further comprising the step of:
joining the free ends of said vector arms to each other by a method selected from the group consisting of nucleic acid ligase mediated ligation, complementary sequence annealing, topoisomerase mediated ligation, in vitro site-specific recombination, in vivo site-specific recombination, and in vivo homologous recombination.
4. A method of molecular cloning comprising:
(A) incubating a nucleic acid insert molecule comprising a 5′-hydxoxyl group at one end and a 5′-phosphate at the other end, and a linear double stranded cloning vector, wherein the linear cloning vector comprises a covalently bound topoisomerase polypeptide at one end only and a ligation substrate site at the other end, under conditions sufficient for the covalent joining of said insert to said vector to form a ligated circular vector comprising said linear cloning vector and said insert molecule; and
(B) transforming the ligated circular vector of step (A) into a host cell to obtain transformants.
5. The method of claim 3 wherein said joining of the free ends of said left and right vector arms comprises in vivo site-specific recombination.
6. The method of claim 5 wherein the free end of each of said left and right vector arms that is not joined to said insert molecule comprises a loxP site, and wherein said transforming step (B) comprises transforming the covalently joined molecule of step (A) into a host cell comprising Cre recombinase, wherein said transforming results in in vivo site-specific recombination between the free end of said left vector arm and the free end of said right vector arm to generate a circularized vector molecule.