Oligonucleotide sizing using cleavable primers

• US 5,830,655 A
• Filed: 04/26/1996
• Issued: 11/03/1998
• Est. Priority Date: 05/22/1995
• Status: Expired due to Term

• Current Assignee: Agena Bioscience Inc. (Mesa Laboratories Inc.)
• Original Assignee: SRI International, Inc.
• Inventors: Monforte, Joseph Albert, Shaler, Thomas Andrew, Pollart, Daniel Joseph, Becker, Christopher Hank
• Primary Examiner(s): Horlick, Kenneth R.
• Assistant Examiner(s): Tung, Joyce
• Application Number:
  US08/639,363
• Time in Patent Office: 921 Days
• Field of Search: 435/6, 435/91.2, 435/395, 436/178, 536/24.3
• US Class Current: 435/6.11
• CPC Class Codes: C12Q 1/6816 characterised by the detection means C12Q1/6804 takes precedence
• CPC Class Codes: C12Q 1/6853 using modified primers or templates
• CPC Class Codes: C12Q 1/6858 Allele-specific amplification
• CPC Class Codes: C12Q 1/6869 Methods for sequencing
• CPC Class Codes: C12Q 1/6872 involving mass spectrometry
• CPC Class Codes: C12Q 2521/301 Endonuclease
• CPC Class Codes: C12Q 2523/319 Photocleavage, photolysis, photoactivation
• CPC Class Codes: C12Q 2525/131 incorporating a restriction site
• CPC Class Codes: C12Q 2533/101 Primer extension
• CPC Class Codes: C12Q 2563/167 Mass label
• CPC Class Codes: C12Q 2565/518 characterised by the immobilisation of the nucleic acid sample or target
• CPC Class Codes: C12Q 2565/627 being a mass spectrometer
• CPC Class Codes: Y02A 50/30 Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
• CPC Class Codes: Y10T 436/255 including use of a solid sorbent, semipermeable membrane, or liquid extraction

Abstract

The present invention provides modified oligonucleotide primers designed to incorporate a cleavable moiety so that a 3'"'"' portion of the primer (linked to an extension product) can be released from an upstream 5'"'"' portion of the primer. Upon selective cleavage of the cleavable site, primer extension products that contain about five or fewer base pairs of the primer sequence are released, to provide more useful sizing and sequence information per fragment than extension products containing the entire primer.

Claims

1. A method for determining the size of a primer extension product, comprising:

(a) hybridizing a primer with a target nucleic acid, where said primer (i) is complementary to said target nucleic acid;

(ii) has a first region containing the 5'"'"' end of the primer, and (iii) has a second region containing the 3'"'"' end of the primer, where the 3'"'"' end is capable of serving as a priming site for enzymatic extension and where said second region contains a selected cleavable site,

(b) extending the primer enzymatically to generate a polynucleotide mixture containing an extension product composed of the primer and an extension segment;

(c) cleaving said extension product at the cleavable site to release said extension segment; and

(d) sizing the extension segment by mass spectrometry, whereby said cleaving is effective to increase the read length of the extension segment relative to the read length of the product of (b).

2. The method of claim 1, where said target nucleic acid contains an immobilization attachment site and is thereby immobilized by attachment to a solid support.

3. The method of claim 2, where the target nucleic acid is immobilized prior to said extending.

4. The method of claim 2, where the target nucleic acid is immobilized prior to said cleaving.

5. The method of claim 1, where the cleavable site is a nucleotide capable of blocking 5'"'"' to 3'"'"'enzyme-promoted digestion, and where said cleaving is carried out by digesting the first region of the primer with an enzyme having a 5'"'"' to 3'"'"' exonuclease activity.

6. The method of claim 1, where the cleavable site is located at or within about five nucleotides from the 3'"'"' end of said primer.

7. The method of claim 6, where the second region of said primer is a single nucleotide that also contains the cleavable site.

8. The method of claim 7, where said second region is a ribonucleotide.

9. The method of claim 1, where the cleavable site is selected from the group consisting of dialkoxysilane, 3'"'"'-(S)-phosphorothioate, 5'"'"'-(S)-phosphorothioate, 3'"'"'-(N)-phosphoramidate, 5'"'"'-(N)phosphoramidate, uracil, and ribose.

10. The method of claim 1, where the enzyme for extending the primer in step (b) is a DNA polymerase.

11. The method of claim 4, which further comprises separating the product of (b) from said immobilized target nucleic acid prior to said cleaving step.

12. The method of claim 1, where said sizing is by time-of-flight mass spectrometry.

13. The method of claim 1, where said extending is carried out in the presence of a nucleotide containing (i) an immobilization attachment site and (ii) a releasable site, which is thereby incorporated into said extension segment.

14. The method of claim 13, further comprising, prior to said sizing,

immobilizing said extension segment at the immobilization attachment site, and

releasing said extension segment at said releasable site.

15. A method for determining the size of a primer extension product, comprising:

(a) hybridizing a primer with a target nucleic acid, where said primer (i) is complementary to said target nucleic acid;

(ii) has a first region containing the 5'"'"' end of the primer, and an immobilization attachment site, where the immobilization attachment site of the primer is composed of a series of bases complementary to an intermediary oligonucleotide, and (iii) has a second region containing the 3'"'"' end of the primer, where the 3'"'"' end is capable of serving as a priming site for enzymatic extension and where said second region contains a selected cleavable site,

(b) extending the primer enzymatically to generate a polynucleotide mixture containing an extension product composed of the primer and an extension segment;

(c) cleaving said extension product at the cleavable site to release said extension segment, where prior to said cleaving the primer is immobilized by specific hybridization of the immobilization attachment site to said intermediary oligonucleotide bound to a solid support; and

(d) sizing the extension segment by mass spectrometry, whereby said cleaving is effective to increase the read length of the extension segment relative to the read length of the product of (b).

16. A method for determining the size of a primer extension product, comprising:

(a) combining first and second primers with a target nucleic acid, under conditions that promote hybridization of the primers to the nucleic acid, generating primer/nucleic acid complexes,

where said first primer (i) has a 5'"'"' end and a 3'"'"' end, (ii) is complementary to said target nucleic acid, (iii) has a first region containing the 5'"'"' end of the first primer and (iv) has a second region containing the 3'"'"' end of the first primer, where said 3'"'"' end is capable of serving as a priming site for enzymatic extension and where said second region contains a cleavable site,

and where said second primer (i) has a 5'"'"' end and a 3'"'"' end, (ii) is homologous to said target nucleic acid, (iii) has a first segment containing the 3'"'"' end of the second primer, and (iv) has a second segment containing the 5'"'"' end of the second primer and an immobilization attachment site,

(b) converting the primer/nucleic acid complexes to double-stranded fragments in the presence of a DNA polymerase and deoxynucleoside triphosphates,

(c) amplifying the primer-containing fragments by successively repeating the steps of (i) denaturing said double-stranded fragments to produce single-stranded fragments, (ii) hybridizing said single stranded fragments with said first and second primers to form strand/primer complexes, (iii) generating amplification products from the strand/primer complexes in the presence of DNA polymerase and deoxynucleoside triphosphates, and (iv) repeating steps (i) to (iii) until a desired degree of amplification has been achieved,

(d) immobilizing amplification products containing the second primer via said immobilization attachment site,

(e) removing non-immobilized amplified fragments,

(f) cleaving said immobilized amplification products at the cleavable site, to generate a mixture including a double-stranded product,

(g) denaturing the double-stranded product to release the extension segment, and

(h) sizing the extension segment by mass spectrometry, whereby said cleaving is effective to increase the read length of the extension segment relative to the read length of the amplified strand-primer complexes of (c).

17. A method for determining a single base fingerprint of a target DNA sequence, comprising:

(a) hybridizing a primer with a target DNA, where said primer (i) is complementary to said target DNA;

(ii) has a first region containing the 5'"'"' end of the primer and an immobilization attachment site, and (iii) has a second region containing the 3'"'"' end of the primer, where the 3'"'"' end is capable of serving as a priming site for enzymatic extension and where said second region contains a selected cleavable site,

(b) extending the primer with an enzyme in the presence of a dideoxynucleoside triphosphate corresponding to said single base, to generate a polynucleotide mixture of primer extension products, each product containing a primer and an extension segment;

(c) cleaving said extension products at the cleavable site to release said extension segments, where prior to said cleaving the primers are immobilized at said immobilization attachment sites;

(d) sizing the extension segments by mass spectrometry, whereby said cleaving is effective to increase the read length of any given extension segment relative to the read length of its corresponding primer extension product of (b), and

(e) determining the positions of said single base in said target DNA by comparison of the sizes of the extension segments.

18. A method for determining an adenine fingerprint of a target DNA sequence, comprising:

(a) hybridizing a primer with a DNA target, where said primer (i) is complementary to said target DNA;

(ii) has a first region containing the 5'"'"' end of the primer and an immobilization attachment site, and (iii) has a second region containing the 3'"'"' end of the primer, where the 3'"'"' end is capable of serving as a priming site for enzymatic extension and where said second region contains a selected cleavable site,

(b) extending the primer with an enzyme in the presence of deoxyadenosine triphosphate (dATP), deoxythymidine triphosphate (dTTP), deoxycytidine triphosphate (dCTP), deoxyguanosine triphosphate (dGTP), and deoxyuridine triphosphate (dUTP), to generate a polynucleotide mixture of primer extension products containing dUTP at positions corresponding to dATP in said target, each product containing a primer and an extension segment;

(c) treating said primer extension products with uracil DNA-glycosylase to fragment specifically at dUTP positions to produce a set of primer extension degradation products,

(d) washing said primer extension degradation products, where prior to said washing, the primer extension degradation products are immobilized at said immobilization attachment sites, each immobilized primer extension degradation product containing a primer and an extension segment, where said washing is effective to remove non-immobilized species,

(e) cleaving said immobilized primer extension degradation products at the cleavable site to release said extension segments,

(f) sizing the extension segments by mass spectrometry, whereby said cleaving is effective to increase the read length of any given extension segment relative to the read length of its corresponding primer extension degradation product, and

(g) determining the positions of adenine in said target DNA by comparison of the sizes of the released extension segments.