Novel allelic variant of CYP2C19 associated with drug metabolism
AssigneesCouncil of Scientific and Industrial Research, Nicholas Piramal India Limited
InventorsBrahmachari Kumar, Kukreti Ritushree, Mukerji Mitali, Martis Suparna, Fernandes Ravina, Sharma Nitin
Life of this patent
Estimating the term…
Abstract
The invention provides methods, PCR primers and sequence determination oligonucleotides for determining a human's capacity to metabolise a substrate of the CYP2C19 enzyme using genetic analysis.
Claims15
A novel allelic variant CYP2C19*2C of CYP2C19 gene encoding the drug metabolizing enzyme CYP2C19 comprising SEQ ID No.24.
A novel polymorph of the CYP2C19 drug metabolizing enzyme comprising amino acid sequence of SEQ ID No. 23.
A set of novel PCR primers useful for detection of the novel polymorphism of C518T comprising SEQ ID No. 2 and SEQ ID No. 3, wherein:
- forward primer:
- (SEQ ID No. 2)
- 5′ ATCCCCAACTATTCTCACCCTTTCTA 3′,
- reverse primer:
- (SEQ ID No. 3)
- 5′ GATATTCACCCCATGGCTGTCTA 3′.
A set of novel sequence determination oligonucleotide (SNap Short Primers) useful for detection of the novel polymorphism of C518T comprising SEQ ID No. 12 and SEQ ID No. 14, wherein:
- forward primer:
- (SEQ ID No. 12)
- 5′ CCACTTTCATCCTGGGCTGTG3′
- reverse primer:
- (SEQ ID No.14)
- 5′ GGAGCAGATCACATTGCAGGGA3′.
A method for predicting the capacity of a drug dose to metabolize a substrate of a CYP2C19 enzyme in a human subject from indian population, wherein the said method comprising the steps of
- (a) preparing the nucleic acid template for identifying the polymorphism at positions 518 of SEQ ID NO:
- 2 and 3 comprising:
- (i) isolating double stranded DNA from the subject;
- (ii) PCR amplification of the DNA wherein the amplified DNA encodes exon 4 of CYP2C19 gene present on each homologous chromosome 10 of the subject as set forth in SEQ ID NO. 2 and 3 respectively;
- (iii) purifying said amplified DNA by polyethylene glycol precipitation;
- (b) detecting polymorphism using extension primers (Snap short primers) having SEQ ID No. 12 and 14;
- (c) relating the labeled nucleic acid to the identity of the said polymorphism in the subject and validating the polymorphism by high throughput mass array detector using PCR primers comprising SEQ ID No. 26 and SEQ ID No. 27 and extension primer having SEQ ID 28, wherein:
- forward primer:
- (SEQ ID No. 26)
- 5′ ACGTTGGATGCTGTAAGTGGTTTCTCAGGA3′
- reverse primer:
- (SEQ ID No. 27)
- 5′ ACGTTGGATGCCAATCATTTAGCTTCACCC3′
- extension primer:
- (SEQ ID NO. 28)
- 5′ AGATCACATTGCAGGGA3′
- wherein the presence of C518T polymorphism predicts the poor/intermediate drug metabolism mediated by CYP2C19 enzyme.
A kit useful for the prediction of CYP2C19 enzyme mediated drug metabolism comprising:
- e) a set of oligonucleotide PCR primers suitable for amplifying the polymorphic region corresponding to position 518 or exon 4 of SEQ ID NO:
- 2 and 3;
- f) a set of sequence determination oligonucleotides for detecting polymorphism at position 518 of SEQ ID NO:
- 12 and 14;
- g) a polymerizing agent and fluorescently labeled chain terminating nucleotides;
- h) buffers, vials and microtiter plates.
A method comprising using a novel allelic variant having SEQ ID No.24 CYP2C19*2C of CYP2C19 gene for the prediction of CYP2C19 enzyme mediated drug metabolism.
Dependencies are inferred from the claim text.