Methods for the isothermal amplification of nucleic acid molecules

Claim 1

A method for amplifying a target polynucleotide region of a double-stranded nucleic acid molecule present in a sample, said method comprising: (A) incubating said sample under conditions sufficient to separate the strands of said double-stranded molecule and thereby form single-stranded nucleic acid molecules; (B) incubating said formed single-stranded nucleic acid molecules in the presence of first primer molecules, said first primer molecules being single-stranded, and comprising from 3' terminus to 5' terminus: (1) a first polynucleotide region complementary to the 3' terminus of said target polynucleotide region; (2) a second polynucleotide region containing modified nucleotides, said modified nucleotides being selected from the group consisting of methylated nucleotides and (α-thio)phosphorothioate nucleotides, wherein, if said second polynucleotide region were hybridized to a complementary polynucleotide, a double-stranded polynucleotide would thereby be formed that would contain one or more restriction endonuclease cleavage sites not present in said target polynucleotide region that would be recognized by a restriction endonuclease that is substantially incapable of cleaving a strand of a nucleic acid molecule that contains said modified nucleotides; (3) a third polynucleotide region, wherein, if said third polynucleotide region were hybridized to a complementary polynucleotide, a double-stranded polynucleotide would thereby be formed that would contain a lox site; wherein said incubation is conducted in the presence of a polymerase and nucleotides lacking the modification of the modified nucleotides present in said first primer, said incubation being under conditions sufficient to (i) permit said first polynucleotide region of said first primer molecules to hybridize to the 3' terminus of said target polynucleotide, and (ii) permit template dependent extension of said first primer molecules, to thereby form first primer extension products; (C) incubating said first primer extension products under conditions sufficient to separate the strands of double-stranded nucleic acid molecules and thereby produce unhybridized first primer extension products; (D) incubating said produced unhybridized first primer extension products in the presence of second primer molecules, said second primer molecules being single-stranded, and comprising from 3' terminus to 5' terminus: (1) a first polynucleotide region having the sequence of the 5' terminus of said target polynucleotide; (2) a second polynucleotide region, wherein, if said second polynucleotide region were hybridized to a complementary polynucleotide, a double-stranded polynucleotide would thereby be formed that would contain a lox site; wherein said incubation is conducted in the presence of a polymerase and nucleotides lacking the modification of the modified nucleotides present in said first primer, said incubation being under conditions sufficient to (i) permit said unhybridized first primer extension products to hybridize to the 3' terminus of said second primer molecules, and (ii) permit template dependent extension of said first primer extension products, and of said second primer molecules, to thereby form linear double-stranded nucleic acid molecules having a lox site at each end, and containing said target polynucleotide that is to be amplified and a hemi-modified restriction site; (E) incubating the linear double-stranded nucleic acid molecules of step (D) in the presence of Cre recombinase, said restriction endonuclease, said polymerase and said nucleotides lacking the modification of the modified nucleotides present in said first primer; wherein said incubation permits the following reactions to occur: (1) said Cre circularizes said linear double-stranded nucleic acid molecules having a lox site at each end, to thereby form a double-stranded circular molecule; (2) said restriction endonuclease cleaves a non-modified nucleotide-containing strand of said hemi-modified restriction endonuclease recognition site of said double-stranded circular molecule to thereby form an extendible 3' terminus; and (3) said polymerase and said non-modified nucleotides mediate template dependent primer extension of said extendible 3' terminus to thereby cause displacement of a single-stranded polynucleotide containing said target polynucleotide region; said primer extension further resulting in the creation of a new hemi-modified restriction recognition site; and (4) said restriction endonuclease cleaves a non-modified nucleotide-containing strand of said newly created hemi-modified restriction endonuclease recognition site to thereby form a new extendible 3' terminus, and permit the release of said single-stranded polynucleotide containing said target polynucleotide region, wherein said displacement and said release accomplishes said desired amplification of said target polynucleotide; and (F) maintaining said incubation conditions of step (E) until a desired level of amplification of said target polynucleotide has been attained.

Claim 2

A method for amplifying a target polynucleotide region of a double-stranded nucleic acid molecule present in a sample, said method comprising: (A) incubating said sample under conditions sufficient to separate the strands of said double-stranded molecule and thereby form single-stranded nucleic acid molecules; (B) incubating said formed single-stranded nucleic acid molecules in the presence of first primer molecules, said first primer molecules being single-stranded, and comprising from 3' terminus to 5' terminus: (1) a first polynucleotide region complementary to the 3' terminus of said target polynucleotide region; (2) a second polynucleotide region containing modified nucleotides, said modified nucleotides being selected from the group consisting of methylated nucleotides and (α-thio)phosphorothioate nucleotides, wherein, if said second polynucleotide region were hybridized to a complementary polynucleotide, a double-stranded polynucleotide would thereby be formed that would contain one or more restriction endonuclease cleavage sites not present in said target polynucleotide region that would be recognized by a restriction endonuclease that is substantially incapable of cleaving a strand of a nucleic acid molecule that contains said modified nucleotides; (3) a third polynucleotide region, wherein, if said third polynucleotide region were hybridized to a complementary polynucleotide, a double-stranded polynucleotide would thereby be formed that would contain a lox site; wherein said incubation is conducted in the presence of a polymerase and nucleotides lacking the modification of the modified nucleotides present in said first primer, said incubation being under conditions sufficient to (i) permit said first polynucleotide region of said first primer molecules to hybridize to the 3' terminus of said target polynucleotide, and (ii) permit template dependent extension of said first primer molecules, to thereby form first primer extension products; (C) incubating said first primer extension products under conditions sufficient to separate the strands of double-stranded nucleic acid molecules and thereby produce unhybridized first primer extension products; (D) incubating said produced unhybridized first primer extension products in the presence of second primer molecules, said second primer molecules being single-stranded, and comprising from 3' terminus to 5' terminus: (1) a first polynucleotide region having the sequence of the 5' terminus of said target polynucleotide; (2) a second polynucleotide region, wherein, if said second polynucleotide region were hybridized to a complementary polynucleotide, a double-stranded polynucleotide would thereby be formed that would contain a lox site; wherein said incubation is conducted in the presence of a polymerase and nucleotides lacking the modification of the modified nucleotides present in said first primer, said incubation being under conditions sufficient to (i) permit said unhybridized first primer extension products to hybridize to the 3' terminus of said second primer molecules, and (ii) permit template dependent extension of said first primer extension products, and of said second primer molecules, to thereby form linear double-stranded nucleic acid molecules having a lox site at each end, and containing said target polynucleotide that is to be amplified and a hemi-modified restriction site; (E) incubating the linear double-stranded nucleic acid molecules of step (D) in the presence of Cre recombinase, said restriction endonuclease, said polymerase and said nucleotides lacking the modification of the modified nucleotides present in said first primer; wherein said incubation permits the following reactions to occur: (1) said Cre circularizes said linear double-stranded nucleic acid molecules having a lox site at each end, to thereby form a double-stranded circular molecule; (2) said restriction endonuclease cleaves a non-modified nucleotide-containing strand of said hemi-modified restriction endonuclease recognition site of said double-stranded circular molecule to thereby form an extendible 3' terminus; and (3) said polymerase and said non-modified nucleotides mediate template dependent primer extension of said extendible 3' terminus to thereby cause displacement of a single-stranded polynucleotide containing said target polynucleotide region; said primer extension further resulting in the creation of a new hemi-modified restriction recognition site; and (4) said restriction endonuclease cleaves a non-modified nucleotide-containing strand of said newly created hemi-modified restriction endonuclease recognition site to thereby form a new extendible 3' terminus, and permit the release of said single-stranded polynucleotide containing said target polynucleotide region, wherein said displacement and said release accomplishes said desired amplification of said target polynucleotide; and (F) maintaining said incubation conditions of step (E) until a desired level of amplification of said target polynucleotide has been attained.

Claim 10

A method for amplifying a target polynucleotide region of a double-stranded nucleic acid molecule present in a sample, which comprises the steps: (A) incubating linear double-stranded nucleic acid molecules in the presence of a polymerase, nucleotides, a Cre recombinase, a primer and a restriction endonuclease; (i) wherein each of said linear double-stranded nucleic acid molecules has two ends and comprises: (a) a first lox site located at a first end of said linear molecule, (b) a second lox site located at a second end of said linear molecule, wherein said first and said second lox sites are oriented in a directly repeated orientation with respect to one another so as to permit said Cre to mediate the circularization of said linear double-stranded molecules, and to thereby form double-stranded circular molecules; (c) said target polynucleotide region located internal to said first and second lox sites, (d) a hemi-modified restriction site located between said target polynucleotide region and one of said lox sites, wherein one strand of said hemi-modified restriction site of each of said linear molecules contains modified nucleotides, said modified nucleotides being selected from the group consisting of methylated nucleotides and (α-thio)phosphorothioate nucleotides; (ii) wherein said target polynucleotide region lacks a site that can be cleaved by said restriction endonuclease, and wherein said restriction endonuclease is substantially incapable of cleaving a strand of a nucleic acid molecule that contains said modified nucleotides; (iii) wherein said primer comprises from 3' terminus to 5' terminus: (a) a first polynucleotide region complementary to a 3' terminal portion of said target polynucleotide region; (b) a second polynucleotide region containing modified nucleotides, said modified nucleotides being selected from the group consisting of methylated nucleotides and (α-thio)phosphorothoiate nucleotides, wherein, if said second polynucleotide region were hybridized to a complementary polynucleotide, a double-stranded polynucleotide would thereby be formed that would contain one or more restriction endonuclease cleavage sites that would be recognized by said restriction endonuclease; (c) a third polynucleotide region, wherein, if said third polynucleotide region were hybridized to a complementary polynucleotide, a double-stranded polynucleotide would thereby be formed that would contain a lox site; and (iv) wherein said incubation is conducted under conditions suitable for permitting: (a) said Cre to circularize said linear double-stranded nucleic acid molecules and thereby form said double-stranded circular molecules; (b) said restriction endonuclease to cleave one strand of said hemi-modified restriction endonuclease recognition site of said double-stranded circular molecule and thereby create an extendible 3' terminus; (c) said polymerase and said nucleotides to mediate template dependent extension of said extendible 3' terminus and thereby cause displacement of a single-stranded polynucleotide containing said target polynucleotide region; said extension further resulting in the creation of a new hemi-modified restriction recognition site; (d) said restriction endonuclease to cleave one strand of said newly created hemi-modified restriction endonuclease recognition site and thereby form a new extendible 3' terminus and permit the release of said single-stranded polynucleotide containing said target polynucleotide region; and (e) said primer to hybridize to said released single-stranded polynucleotide and to be extended by said polymerase and said nucleotides in a template dependent extension to thereby form an additional copy of said linear double-stranded nucleic acid molecule; thereby amplifying said target polynucleotide region of said double-stranded nucleic acid molecule; and (B) maintaining said incubation conditions until a desired level of amplification of said target polynucleotide region of said double-stranded nucleic acid molecule has been attained.

Claim 11

A method for amplifying a target polynucleotide region of a double-stranded nucleic acid molecule present in a sample, which comprises the steps: (A) incubating linear double-stranded nucleic acid molecules in the presence of a polymerase, nucleotides, a Cre recombinase, a primer and a restriction endonuclease; (i) wherein each of said linear double-stranded nucleic acid molecules has two ends and comprises: (a) a first lox site located at a first end of said linear molecule, (b) a second lox site located at a second end of said linear molecule, wherein said first and said second lox sites are oriented in a directly repeated orientation with respect to one another so as to permit said Cre to mediate the circularization of said linear double-stranded molecules, and to thereby form double-stranded circular molecules; (c) said target polynucleotide region located internal to said first and second lox sites, (d) a hemi-modified restriction site located between said target polynucleotide region and one of said lox sites, wherein one strand of said hemi-modified restriction site of each of said linear molecules contains modified nucleotides, said modified nucleotides being selected from the group consisting of methylated nucleotides and (α-thio)phosphorothioate nucleotides; (ii) wherein said target polynucleotide region lacks a site that can be cleaved by said restriction endonuclease, and wherein said restriction endonuclease is substantially incapable of cleaving a strand of a nucleic acid molecule that contains said modified nucleotides; (iii) wherein said primer comprises from 3' terminus to 5' terminus: (a) a first polynucleotide region complementary to a 3' terminal portion of said target polynucleotide region; (b) a second polynucleotide region containing modified nucleotides, said modified nucleotides being selected from the group consisting of methylated nucleotides and (α-thio)phosphorothoiate nucleotides, wherein, if said second polynucleotide region were hybridized to a complementary polynucleotide, a double-stranded polynucleotide would thereby be formed that would contain one or more restriction endonuclease cleavage sites that would be recognized by said restriction endonuclease; (c) a third polynucleotide region, wherein, if said third polynucleotide region were hybridized to a complementary polynucleotide, a double-stranded polynucleotide would thereby be formed that would contain a lox site; and (iv) wherein said incubation is conducted under conditions suitable for permitting: (a) said Cre to circularize said linear double-stranded nucleic acid molecules and thereby form said double-stranded circular molecules; (b) said restriction endonuclease to cleave one strand of said hemi-modified restriction endonuclease recognition site of said double-stranded circular molecule and thereby create an extendible 3' terminus; (c) said polymerase and said nucleotides to mediate template dependent extension of said extendible 3' terminus and thereby cause displacement of a single-stranded polynucleotide containing said target polynucleotide region; said extension further resulting in the creation of a new hemi-modified restriction recognition site; (d) said restriction endonuclease to cleave one strand of said newly created hemi-modified restriction endonuclease recognition site and thereby form a new extendible 3' terminus and permit the release of said single-stranded polynucleotide containing said target polynucleotide region; and (e) said primer to hybridize to said released single-stranded polynucleotide and to be extended by said polymerase and said nucleotides in a template dependent extension to thereby form an additional copy of said linear double-stranded nucleic acid molecule; thereby amplifying said target polynucleotide region of said double-stranded nucleic acid molecule; and (B) maintaining said incubation conditions until a desired level of amplification of said target polynucleotide region of said double-stranded nucleic acid molecule has been attained.