Method of quick screening and identification of specific DNA sequences by single nucleotide primer extension and kits therefor

• US 5,710,028 A
• Filed: 10/04/1994
• Issued: 01/20/1998
• Est. Priority Date: 07/02/1992
• Status: Expired due to Term

• Current Assignee: Diagenetics Limited
• Original Assignee: Diagenetics Limited
• Inventors: Eyal, Nurit, Navot, Nir
• Primary Examiner(s): Jones, W. Gary
• Assistant Examiner(s): TRAN, PAUL
• Application Number:
  US08/317,432
• Time in Patent Office: 1,204 Days
• Field of Search: 435/6, 435/91.1, 935/77, 935/78, 536/24.33, 536/26.66
• US Class Current: 435/91.1
• CPC Class Codes: C07K 14/4712 Cystic fibrosis
• CPC Class Codes: C12Q 1/6858 Allele-specific amplification
• CPC Class Codes: C12Q 2525/186 incorporating a non-extendable or blocking moiety
• CPC Class Codes: C12Q 2563/131 the label being a member of a cognate binding pair, i.e. extends to antibodies, haptens, avidin

Abstract

A method of simultaneous determination of the identity of nucleotide bases at specific positions in nucleic acids of interest, which includes (a) treating a sample containing the nucleic acids of interest to obtain unpaired nucleotide bases spanning the specific positions, if the nucleic acids are not already single stranded; (b) contacting the unpaired nucleotide bases with combinations of various marked oligonucleotide primers each for hybridizing with a stretch of nucleotide bases present in each nucleic acid of interest immediately adjacent the nucleotide base to be identified, so as to form a duplex between the primer and the nucleic acid of interest such that the nucleotide base to be identified is the first unpaired base in the template immediately 5'"'"' of the nucleotide base annealed with the 3'"'"'-end of the primer in the duplex; (c) contacting the duplex with the reagent which includes an aqueous carrier, and at least one primer extension unit, the primer extension unit including an extension moiety a separation moiety and a detection moiety, with the extension moiety for specifically halting a nucleic acid template dependent, primer extension reaction, in a manner which is strictly dependent on the identity of the unpaired nucleotide base of the template immediately adjacent to, and 3'"'"' of, the 3'"'"'-end of the primer, with the separation moiety permitting the affinity separation of the primer extension unit from unincorporated, or non-extended, primers, and with the detection moiety enabling the direct or indirect detection of the presence of a primer extension unit the contacting taking place under conditions permitting the base pairing of the complementary extension moiety of the primer extension unit present in the reagent with the nucleotide base to be identified and the occurrence of a template dependent, primer extension reaction to incorporate the extension moiety of the primer extension unit at the 3'"'"'-end of the primer, resulting in the extension of the primer by a single unit; (d) removing the non-extended marked primer; (e) determining the presence of a nucleotide alteration; and (f) determining the identity of the extended primers, and therefore the kind of alterations and the complete genotype of the examined nucleic acid, by hybridizing the extended primers to complementary oligonucleotides adhered to a test surface.

Claims

1. A method of determining the identity of a nucleotide base at a specific position in a nucleic acid of interest, which can be used to detect point mutations, allelism, and the genotype of an examined individual, comprising the steps of:

(a) if the nucleic acid of interest is double stranded, treating said double stranded nucleic acid to obtain single stranded nucleotide bases spanning the specific position, or, if the nucleic acid of interest is single stranded, directly employing step (b);

(b) contacting said single stranded nucleotide bases spanning the specific position with an oligonucleotide primer having a 3'"'"'-end, said primer being for hybridizing with single stranded stretches of nucleotide bases present in the nucleic acid of interest adjacent the nucleotide base to be identified, so as to form a duplex between the primer and the nucleic acid of interest;

(c) contacting, in the presence of a template dependent extension enzyme, said duplex with;

(i) a primer extension unit, said primer extension unit including an extension moiety for specifically halting a nucleic acid template dependent primer extension reaction, in a manner which is strictly dependent on the identity of an unpaired nucleotide base of the nucleic acid of interest located within the nucleic acid of interest 5'"'"' to the specific position, for permitting base pairing of said extension moiety of said primer extension unit with said unpaired nucleotide base, said oligonucleotide primer and said primer extension unit are selected such that any nucleotide bases of the nucleic acid of interest present between said 3'"'"'-end of said oligonucleotide primer and said unpaired nucleotide base are different from said unpaired nucleotide base; and

(ii) one to three additional primer extension units, each of said one to three additional primer extension units having an extension moiety permitting primer extension, said one to three additional primer extension units are selected such that each is complementary to at least one of said nucleotide bases of the nucleic acid of interest present between said 3'"'"'-end of said oligonucleotide primer and said unpaired nucleotide base, among which at least the nucleotide base at the specific position being present;

such that said template dependent primer extension reaction is initiated by incorporation of said one to three additional primer extension units and is halted by incorporation of said primer extension unit which has said extension moiety for specifically halting said nucleic acid template dependent primer extension reaction; and

(d) determining the presence of an extended primer.

2. A method as in claim 1, wherein said extension moiety of said primer extension unit is by itself not sufficient for halting said primer extension reaction, said primer extension reaction is halted by limiting said one to three additional primer extension units to one to two additional primer extension units.

3. A method as in claim 1, wherein said extension moiety of said primer extension unit is by itself sufficient for halting said primer extension reaction.

4. A method as in claim 1, wherein said oligonucleotide primer includes a detection group for facilitating said determination of said presence of said extended primer.

5. A method as in claim 1, wherein said primer extension unit which includes said extension moiety, itself for specifically halting said nucleic acid template dependent primer extension reaction, further includes a separation moiety for permitting affinity separation of said extended primer from non-extended primers.

6. A method as in claim 1, wherein following step (c) an additional step of cycling the reaction, is provided, by repeatedly exposing the reaction to

(a) a denaturing condition under which said extended primer is separated from the nucleic acid of interest;

followed by

(b) a condition permitting said template dependent primer extension reaction to take place.

7. A method as in claim 1, wherein said 3'"'"'-end of said oligonucleotide primer is located immediately adjacent to, and 3'"'"' of the nucleotide base at the specific position, such that no nucleotide bases are present within the nucleic acid of interest between said 3'"'"'-end of said primer and said specific position.