Primer extension target enrichment and improvements thereto including simultaneous enrichment of DNA and RNA

Patent metadata

Field	Value
Publication number	US-11499180-B2
Application number	US-201916549962-A
Country	US
Kind code	B2
Filing date	Aug 23, 2019
Priority date	Mar 8, 2017
Publication date	Nov 15, 2022
Grant date	Nov 15, 2022

Abstract

The present invention is a method and compositions for primer extension target enrichment of nucleic acids and improvements thereto including simultaneously enriching for RNA and DNA and optionally sequencing the enriched products. An embodiment of the present invention includes a method comprising the steps of: hybridizing a target-specific primer to a target DNA or RNA, wherein the primer comprises a target-binding region and a region of complementarity to an adaptor; extending the primer with a DNA polymerase or reverse transcriptase to form a primer extension product; contacting the product with an adaptor comprising a longer strand with a 5′-overhang having complementarity to said primer and a shorter strand comprising a universal priming site; hybridizing the adaptor to the product; and ligating one strand of the adaptor to the product to form a ligation product.

First claim

We claim:

1. A method of simultaneously enriching a target polynucleotide from a sample, wherein the method comprises:
(a) providing a sample comprising the target polynucleotide in both single-stranded RNA form and double-stranded DNA form;
(b) hybridizing a first target-specific primer to the single-stranded RNA form of the target polynucleotide, wherein the first target-specific primer comprises a target-binding region and a region of complementarity to an adaptor;
(c) extending the hybridized first target-specific primer with a reverse transcriptase (RT) to form a double-stranded RNA-DNA hybrid, wherein the double-stranded RNA-DNA hybrid comprises an RNA strand and a first primer extension product;
(d) subjecting the sample to double-stranded nucleic acid denaturation conditions;
(e) hybridizing a second target-specific primer to the denatured nucleic acids, wherein the second target-specific primer comprises a target-binding region and a region of complementarity to the adaptor;
(f) extending the hybridized second target-specific primer with a DNA polymerase, to form a second primer extension product;
(g) contacting the sample with the adaptor, wherein the adaptor comprises a longer strand and a shorter strand, wherein the longer strand comprises a region complementary to the region in the first target-specific primer and the second target-specific primer, and the shorter strand comprises a universal priming site;
(h) hybridizing the adaptor to the first primer extension product and the second primer extension product;
(i) ligating one strand of the adaptor to the first primer extension product and the second primer extension product to form ligation products;
(j) hybridizing a third target-specific primer to the first primer extension product, and hybridizing a fourth target-specific primer to the second primer extension product, wherein the third target-specific primer and the fourth target-specific primer comprise a target-binding site and a universal binding site; and
(k) hybridizing primers to the universal binding sites, and amplifying the ligation products.

2. The method of claim 1 , wherein the first target-specific primer and the second target-specific primer comprise unique molecular barcodes (UID).

3. A method of sequencing a target polynucleotide from a sample, wherein the method comprises:
(a) providing a sample comprising the target polynucleotide in both single-stranded RNA form and double-stranded DNA form;
(b) hybridizing a first target-specific primer to the single-stranded RNA form of the target polynucleotide, wherein the first target-specific primer comprises a target-binding region and a region of complementarity with an adaptor;
(c) extending the hybridized first target-specific primer with a reverse transcriptase (RT) to form a double-stranded RNA-DNA hybrid, wherein the double-stranded RNA-DNA hybrid comprises an RNA strand and a first primer extension product;
(d) subjecting the sample to double-stranded nucleic acid denaturation conditions;
(e) hybridizing a second target-specific primer to the denatured nucleic acids, wherein the second-target specific primer comprises a target-binding region and a region of complementarity to an adaptor;
(f) extending the hybridized second target-specific primer with a DNA polymerase to form a second primer extension product;
(g) contacting the sample with the adaptor, wherein the adaptor comprises a longer strand and a shorter strand, wherein the longer strand comprises a region complementary to the region in the first target-specific primer and the second target-specific primer, and the shorter strand comprises a universal priming site;
(h) hybridizing the adaptor to the first primer extension product and the second primer extension product;
(i) ligating one strand of the adaptor to the first primer extension product and the second primer extension product to form ligation products;
(j) hybridizing a third target-specific primer to the first primer extension product, and hybridizing a fourth target-specific primer to the second primer extension product, wherein the third target-specific primer and the fourth target-specific primer comprise a target-binding site and a universal priming site;
(k) hybridizing primers to the universal priming sites, and amplifying the ligation products; and
(l) sequencing the amplified ligation products from step (k).

4. The method of claim 3 , wherein the universal primer is used as a sequencing primer.

5. The method of claim 3 , wherein the third target-specific primer and the fourth target-specific primer further comprise a sequencing primer binding site.

6. The method of claim 3 , wherein the adaptor further comprises a sequencing primer-binding site.

7. The method of claim 3 , wherein the adaptor further comprises a barcode.

8. A method of simultaneously enriching a target polynucleotide from a sample, wherein the method comprises:
(a) providing a sample comprising the target polynucleotide in both single-stranded RNA form and double-stranded DNA form;
(b) hybridizing a first target-specific primer to the single-stranded RNA form of the target polynucleotide, wherein the first target-specific primer comprises a target-binding region;
(c) extending the hybridized first target-specific primer with a reverse transcriptase (RT) to form a double-stranded RNA-DNA hybrid, wherein the double-stranded RNA-DNA hybrid comprises an RNA strand and a first primer extension product;
(d) subjecting the sample to double-stranded nucleic acid denaturation conditions;
(e) hybridizing a second target-specific primer to the denatured nucleic acids, wherein the second target-specific primer comprises a target-binding region and a region of complementarity to an adaptor;
(f) hybridizing a third target-specific primer to the first primer extension product, wherein the primer comprises a target-binding region and a region of complementarity to the adaptor;
(g) extending the hybridized second target-specific primer and the third target-specific primer with a DNA polymerase to form a second primer extension product and a third primer extension product;
(h) contacting the sample with the adaptor, wherein the adaptor comprises a longer strand and a shorter strand, wherein the longer strand comprises a region complementary to the region in the target-specific primers, and the shorter strand comprises a universal priming site;
(i) hybridizing the adaptor to the second primer extension product and the third primer extension product;
(j) ligating one strand of the adaptor to the second primer extension product and the third primer extension product, to form ligation products;
(k) hybridizing a fourth target-specific primer to the second primer extension product and hybridizing a fifth target-specific primer to the third primer extension product, wherein the fourth target-specific primer and the fifth target-specific primer comprise a target-binding site and a universal priming site; and
(l) hybridizing primers to the universal priming sites, and amplifying the ligation products.

9. The method of claim 1 , wherein at least one of the first and second target specific primers comprises a barcode selected from a unique molecular barcode (UID) and a sample barcode (SID).

10. The method of claim 1 , wherein the adaptor further comprises a barcode.

11. The method of claim 1 , wherein amplifying in step (k) comprises a digital droplet PCR.

12. The method of claim 1 , wherein the universal primer is used as a sequencing primer.

13. The method of claim 1 , wherein the third target-specific primer and the fourth target-specific primer further comprise a sequ

Assignees

• Roche Sequencing Solutions Inc

Inventors

• Godwin Brian Christopher
• Ozturk Sedide

Classifications

• C12Q1/6869

  Methods for sequencing · CPC title

• C12Q1/6806

  Preparing nucleic acids for analysis, e.g. for polymerase chain reaction [PCR] assay (C12Q1/6804 takes precedence) · CPC title

• C12Q1/6855 Primary

  Ligating adaptors · CPC title