Enrichment of target sequences
View Patent ↗Methods and compositions are provided for enriching for target sequences from a population of nucleic acids, that includes combining in solution, a population of nucleic acids and a target isolation probe wherein the target isolation probe includes an affinity binding domain; permitting a single stranded region of the target isolation probe to hybridize to all or a portion of a target sequence in the population of nucleic acids; selectively immobilizing the hybridized nucleic acids from the population containing the target sequences by associating the target isolation probe with a capture domain and removing unbound material; and removing from the 3′ end of the target sequence, a non-target sequence by means of one or more 3′ single strand specific exonucleases. Target enrichment may be used to detect variations in nucleotide sequence for detecting phenotypic changes related to health or disease.
1. A method for obtaining a target nucleotide sequence of adaptor-ligated target molecules, comprising:
(a) obtaining purified nucleic acids, wherein at least some of the nucleic acids comprise a target sequence and a 3′ non-target sequence;
(b) producing the adaptor-ligated target molecules by:
(i) combining the nucleic acids with a target isolation probe, wherein the target isolation probe is a nucleic acid probe and comprises an affinity binding domain;
(ii) permitting a single stranded region of the target isolation probe to hybridize to all or a portion of the target sequence in the nucleic acids, thereby producing hybridized nucleic acids comprising the 3′ non-target sequence, wherein the 3′ non-target sequence in the hybridized nucleic acids is single stranded;
(iii) enriching the hybridized nucleic acids of step (b) by associating the target isolation probe with a capture domain, thereby producing enriched nucleic acids comprising the hybridized nucleic acids;
(iv) removing the 3′ non-target sequence from the enriched nucleic acids using one or more 3′ single strand-specific exonucleases, thereby producing cleaved enriched nucleic acids; and
(v) ligating an adaptor to the 3′ end of the target sequence of the cleaved enriched nucleic acids after the 3′ non-target sequence is removed in step (iv), thereby producing adaptor-ligated target molecules; and
(c) obtaining the target nucleotide sequence of the adaptor-ligated target molecules.
2. The method according to claim 1 , wherein the target sequence in the enriched nucleic acids of step (b)(iii) comprises a 5′ end that is single stranded, and the method further comprises extending the 3′ end of the target isolation probe in the enriched nucleic acids by a polymerase using the 5′ end of the target sequence as a template.
3. The method according to claim 2 , wherein the method further comprises ligating an adaptor to the 5′ end of the target sequence.
4. The method according to claim 1 , wherein the adaptor is double-stranded.
5. The method according to claim 3 , wherein the adaptor is double stranded.
6. The method according to claim 3 , the method further comprises amplifying the target sequence using primers that hybridize to a sequence in the adaptor or complement thereof.
7. The method according to claim 1 , wherein the purified nucleic acids are from an animal or a plant.
8. The method according to claim 1 , wherein the purified nucleic acids are from a biological fluid.
9. The method according to claim 1 , wherein the target sequence is from a virus, a prokaryote or an eukaryote.
10. The method according to claim 1 , wherein the target sequence is from a tissue biopsy from an eukaryote.
11. The method according to claim 10 , wherein the tissue biopsy is a biopsy of a tissue that is potentially cancerous.
12. The method according to claim 1 , wherein step (b)(i) further comprises combining the nucleic acids with a plurality of target isolation probes, wherein the plurality of target isolation probes comprises the target isolation probe.
13. The method according to claim 1 , wherein at least some of the nucleic acids contains a repeat sequence, and step (b)(i) further comprises combining the nucleic acids with a removable blocking oligonucleotide that hybridizes to the repeat sequence.
14. The method according to claim 1 , wherein the single-stranded region of the target isolation probe in step (b)(ii) hybridizes to a first portion of the target sequence.
15. The method according to claim 1 , wherein an end of the target isolation probe hybridizes with a sequence located in or proximate to the 3′ end or the 5′ end of the target sequence.
16. The method according to claim 1 , further comprising, subsequent to step (b)(ii), permitting hybridization of a single stranded region of an oligonucleotide probe to a second portion of the target sequence.
17. The method according to claim 16 , wherein an end of the oligonucleotide probe forms a duplex with a sequence located in or proximate to the 5′ end or 3′ end of the target sequence but does not form a duplex with the sequences located in or proximate to both the 5′ end and 3′ end of the target sequence.
18. The method according to claim 17 , wherein the target isolation probe hybridizes to one end of the target sequence and the oligonucleotide probe hybridizes to an opposite end of the target sequence such that hybridization of the target isolation probe and the second probe defines the ends of the target sequence.
19. The method according to claim 16 , wherein the target isolation probe or the oligonucleotide probe is a flap probe having: i) a single stranded region that hybridizes to the target sequence, and ii) a double stranded region extending from the 3′ end of the single stranded region.
20. The method according to claim 19 , wherein the double stranded region of the flap probe comprises a 3′-5′ oligonucleotide or the flap probe is a hairpin probe and wherein the method further comprises ligating the 3′-5′oligonucleotide or the hairpin probe to the 5′ end of the target sequence.
21. The method according to claim 1 , further comprising hybridizing an oligonucleotide having a random sequence of 4-10 nucleotides to the nucleic acids.
22. The method according to claim 1 , wherein the enriched nucleic acids of step (b)(iii) further comprise a 5′ single-stranded non-target sequence and the method further comprises removing the 5′ single-stranded non-target sequence from the enriched nucleic acids of step (b)(iii) using a 5′ single-strand specific exonuclease.
23. The method according to claim 22 , further comprising ligating a 3′ end of a double stranded region of an adaptor to the 5′ end of the target sequence.
24. The method according to claim 1 , wherein the adaptor is a hairpin adaptor and step (b)(v) comprising ligating a duplex region of the hairpin adaptor to the 3′ end of the target sequence and the 5′ end of the target isolation probe, thereby covalently linking the target isolation probe to the target sequence.
25. The method according to claim 1 , wherein the affinity binding domain is located between the 3′ and 5′ ends of the target isolation probe and is not located at the 3′ end of the target isolation probe or 5′ end of the target isolation probe.
26. The method according to claim 1 , wherein the adaptor comprises at least one of a sequencing primer site, a library amplification primer site, a unique sample identifier and a unique molecule identifier sequence.
27. The method according to claim 1 , further comprising detecting a mutation in the target sequence.
28. The method according to claim 27 , wherein the mutation is selected from the group consisting of an insertion, deletion, or a single nucleotide polymorphism.