Methods for next generation genome walking and related compositions and kits

Patent metadata

Field	Value
Publication number	US-11795501-B2
Application number	US-202117208538-A
Country	US
Kind code	B2
Filing date	Mar 22, 2021
Priority date	May 22, 2015
Publication date	Oct 24, 2023
Grant date	Oct 24, 2023

Abstract

Methods are provided herein for identifying rare and/or unknown DNA sequences by next-generation sequencing approaches. Isolated double-stranded (ds), single-stranded (ss), or ds/ss DNA is fragmented and the fragments are polished, phosphorylated, and tailed, as necessary. Fragmentation can be enzymatic or mechanical. A universal adapter sequence is ligated to each fragment, wherein the adapter can have a top strand without a 5′ phosphate, a 3′ with an —H in place of the —OH, and/or a 3′ extra base complementary to any base added to the polished fragments. The ligatamers may then serve as templates for amplification using a forward primer complementary to the adapter sequence and a reverse primer targeted to the fragment sequence. Compositions produced by these methods and kits adapted for performing these methods are also described herein.

First claim

What is claimed is:

1. A method for copying a sequence of interest, the method comprising
amplifying a plurality of template polynucleotides, each comprising a randomly fragmented native sequence and a universal adapter sequence on at least one end, the randomly fragmented native sequence comprising the sequence of interest, and the universal adapter sequence comprising 5′ to 3′ a non-primable adapter priming domain and, optionally, a barcode domain consisting of 1 to 20 nucleotides;
wherein the universal adapter sequence is located a fixed distance from the 5′ end of the sequence of interest, such that the nucleotide sequence between the universal adapter sequence and the sequence of interest defines an identification sequence that is unique to a given template and its progeny amplicons, and wherein the universal adapter sequence has a top strand and a non-extendable bottom strand, wherein the bottom strand is non-complementary to a primer sequence of the top strand; and
wherein the amplification is primed with a pair of primers comprising a universal primer that is identical to at least 10 bp of the adapter priming domain of the universal adapter sequence and a first reverse primer that is complementary to a region of the native sequence downstream of the sequence of interest.

2. The method of claim 1 , wherein the sequence of interest is a mutation, a SNP, or an INDEL.

3. The method of claim 1 , further comprising ligating a plurality of universal adapter sequences to a plurality of native sequence polynucleotides to generate the plurality of template polynucleotides.

4. The method of claim 3 , further comprising treating the ligation products with a 3′ to 5′ single-strand specific exonuclease prior to amplifying.

5. The method of claim 1 , further comprising amplifying the amplicons with a pair of primers comprising the universal primer and a second reverse primer that is complementary to a sequence upstream of the region complementary to the first reverse primer.

6. The method of claim 5 , wherein the second reverse primer comprises a 5′ sequencing tag.

7. The method of claim 1 , wherein the template polynucleotides comprise fragmented genomic DNA.

8. The method of claim 1 , wherein the template polynucleotides comprise cDNA.

9. The method of claim 1 , wherein the first reverse primer has a melting temperature that is at least about 5° C., or at least about 10° C. higher than the melting temperature of the universal primer.

10. The method of claim 1 , wherein the adapter priming domain is chosen from one or more of SEQ ID NOS: 1, 19, 40, 74, 75, 112, and 113, and wherein each individual template polynucleotide has a probability greater than 95%, greater than 99%, or greater than 99.9% of being molecularly unique just before the initial amplification step.

Assignees

• Sigma Aldrich Co Llc

Inventors

• Ward Brian

Classifications

• C12Q1/6855 Primary

  Ligating adaptors · CPC title

• C12Q1/68

  involving nucleic acids · CPC title

• C40B20/04

  Identifying library members by means of a tag, label, or other readable or detectable entity associated with the library members, e.g. decoding processes · CPC title

• C12Q2600/156

  Polymorphic or mutational markers · CPC title

• C12Q2600/16

  Primer sets for multiplex assays · CPC title