Detection of nucleic acid sequences
OwnerMohammad ILYAS, James HASSALL +1inventors
InventorsMohammad ILYAS, James HASSALL, Henry EBILI
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Abstract
The invention relates to methods of detecting a target nucleic acid having a variant sequence in a pool of nucleic acid comprising non-variant nucleic acid and/or non-targeted variant nucleic acid, and a method of highly specific PCR, together with associated primers, primers pairs, compositions, kits and uses.
Claims30
A method of detecting one or more target nucleic acid(s) having a variant sequence in a pool of nucleic acid comprising non-variant nucleic acid and/or non-targeted variant nucleic acid, the method comprising:
- providing a forward and reverse PCR primer pair capable of hybridising to the target nucleic acid having a variant sequence for PCR amplification of the target nucleic acid having a variant sequence,
- wherein the terminal 3′ nucleotide of either the forward or reverse primer is arranged to form a base pair with a variant nucleotide of interest in the target nucleic acid sequence having a variant sequence, thereby forming a variant-specific primer, and
- wherein the forward and reverse PCR primers have a minimum annealing temperature (Ta) of 65° C.;
- carrying out a PCR in order to amplify any target nucleic acid having a variant sequence in the pool of the nucleic acid;
- and
- detecting any PCR product or amplification in real-time, wherein the detection of a PCR product or amplification in real-time confirms the presence of the target nucleic acid having a variant sequence in the pool of the nucleic acid.
A method of detecting one or more target nucleic acid(s) having a variant sequence in a pool of nucleic acid that comprises non-variant nucleic acid and/or non-targeted variant nucleic acid, the method comprising:
- i) providing a forward and reverse PCR primer pair capable of hybridising to the target nucleic acid having a variant sequence for PCR amplification of the target nucleic acid having a variant sequence, wherein the forward and reverse PCR primers have a minimum Ta of 65° C.;
- ii) providing a blocking probe that is arranged to hybridise to the variant nucleic acid and/or non-targeted variant nucleic acid and prevent polymerisation from the forward and/or reverse PCR primers;
- carrying out a PCR in order to amplify any target nucleic acid having a variant sequence in the pool of the nucleic acid;
- and
- detecting any PCR product or amplification in real-time, wherein the detection of a PCR product or amplification in real-time confirms the presence of the target nucleic acid having a variant sequence in the pool of the nucleic acid.
A method of highly specific polymerase chain reaction (PCR) amplification of one or more target nucleic acids in a pool of nucleic acid, the method comprising:
- providing a forward and reverse PCR primer pair capable of hybridising to the target nucleic acid for PCR amplification of the target nucleic acid, wherein the forward and reverse PCR primers each comprise a 5′ tag of non-complementary nucleotides and have a minimum annealing temperature (Ta) of 65° C.;
- carrying out a PCR with one or more first cycle temperature profiles, such that the 5′ tag of non-complementary nucleotides of the forward and reverse PCR primer pair become incorporated into the PCR amplicons,
- wherein the first cycle temperature profile provides an annealing temperature of at least 65° C. and which is suitable for the annealing of the forward and reverser primer pair such that they hybridise to the target nucleic acid, and
- carrying out a PCR with one or more second cycle temperature profiles in order to amplify the PCR amplicons from the PCR cycle(s) of the first cycle temperature profile,
- wherein the second cycle temperature profile provides an annealing temperature that is higher than the first cycle temperature profile and which is suitable for the annealing of the PCR amplicons.
The method according to any preceding claim, wherein the forward and reverse PCR primers each comprise a 5′ tag of non-complementary nucleotides.
The method according to any preceding claim, wherein the forward and reverse PCR primers each comprise nucleotide analogues.
The method according to any preceding claim, wherein the forward and/or reverse primer comprise nucleotide analogue selected from LNA, BNA or PNA.
The method according to any preceding claim, wherein the forward or the reverse primer comprises a nucleotide analogue, such as LNA, PNA, or BNA, at the terminal 3′ position.
The method according to any preceding claim, wherein the forward or the reverse primer comprises a nucleotide analogue, such as LNA, PNA, or BNA, at the terminal 3′ position, wherein the remaining primer sequence comprises DNA.
The method according to any preceding claim, wherein the forward or the reverse primer comprises a nucleotide analogue, such as LNA, PNA, or BNA, at the terminal 3′ position, and a 5′ tag of non-complementary nucleotides.
The method according to any preceding claim, wherein the forward and/or reverse primers comprise a GC content of between about 40% and about 60%.
The method according to any preceding claim, wherein the amplification of the PCR product is detected during the PCR, using Real-Time PCR.
A primer for use in a primer pair for detecting a target nucleic acid having a variant sequence in a pool of nucleic acid, wherein the primer is capable of hybridising to the target nucleic acid having a variant sequence for PCR amplification of the target nucleic acid having a variant sequence,
- wherein the terminal 3′ nucleotide of the primer is arranged to base pair with the variant nucleotide of interest in the target nucleic acid having a variant sequence;
- wherein the primer comprises a 5′ tag of non-complementary nucleotides and/or comprise one or more nucleotide analogues such that the primers has a minimum Ta of 65° C.
A forward and reverse primer pair for the PCR detection of a KRAS, PIK3CA, EGFR, APC or BRAF mutation in a target nucleic acid, wherein the forward and/or reverse primer is selected from the KRAS, PIK3CA, EGFR, APC or BRAF forward and reverse primers respectively of table 1 herein
- wherein the forward and reverse primers further comprise a 5′ tag of nucleotides that are non-complementary to the target nucleic acid, and/or wherein terminal 3′ nucleotide of the forward or reverse primer is substituted with a nucleotide analogue.
Dependencies are inferred from the claim text.