Single step PCR for detection of allelic variation of MDR1 gene (P-glycoprotein) among three ethnic groups in Malaysia

Background: P-glycoprotein (PgP) is the most extensively studied ATP-binding cassette (ABC) coded by MDR1 gene. To date, 29 single nucleotide polymorphisms (SNPs) have been identified; but only SNP C3435T has been correlated with intestinal PgP expression levels and shown to influence the absorption...

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Published in:Journal of Clinical Pharmacy and Therapeutics
Main Author: Teh L.K.; Lee W.L.; Amir J.; Salleh M.Z.; Ismail R.
Format: Article
Language:English
Published: 2007
Online Access:https://www.scopus.com/inward/record.uri?eid=2-s2.0-34247881888&doi=10.1111%2fj.1365-2710.2007.00822.x&partnerID=40&md5=72a3352b31c2f55fc8453d234d025736
id 2-s2.0-34247881888
spelling 2-s2.0-34247881888
Teh L.K.; Lee W.L.; Amir J.; Salleh M.Z.; Ismail R.
Single step PCR for detection of allelic variation of MDR1 gene (P-glycoprotein) among three ethnic groups in Malaysia
2007
Journal of Clinical Pharmacy and Therapeutics
32
3
10.1111/j.1365-2710.2007.00822.x
https://www.scopus.com/inward/record.uri?eid=2-s2.0-34247881888&doi=10.1111%2fj.1365-2710.2007.00822.x&partnerID=40&md5=72a3352b31c2f55fc8453d234d025736
Background: P-glycoprotein (PgP) is the most extensively studied ATP-binding cassette (ABC) coded by MDR1 gene. To date, 29 single nucleotide polymorphisms (SNPs) have been identified; but only SNP C3435T has been correlated with intestinal PgP expression levels and shown to influence the absorption of orally taken drugs that are PgP substrates. Individuals homozygous for the T allele have more than fourfold lower PgP expression compared with C/C individuals. We developed a one step primer based allele specific PCR method to detect SNP at C3435T to investigate the distribution of this genotype in the local population. Method: DNA was extracted from 5 mL of whole blood using standard salting-out method. Primers were designed specific to 3′ end which amplify the variants of C3435T. The method was validated by direct DNA sequencing. Seven hundred and sixty-three healthy blood donors comprising of three major ethnic groups in Malaysia were recruited and DNA subjected to genotyping of C3435T using this method. Result: The method was found to be robust and reproducible in detecting SNP of C3435T. Interethnic variations in genotype and allele frequency were observed in PgP among the ethnic groups. In comparison to both the Caucasians and the other Asian countries, the Malay and Chinese showed a higher frequency of allele C (50-60%); while the Indian exhibits a lower frequency (40%), similar to other Indian populations. Discussion and conclusion: Using a new simple method to investigate the distribution of C3435T, we found that the allele frequency of MDR1 showed variablity between the different ethnic groups within the Malaysian population. © 2007 The Authors.

13652710
English
Article
All Open Access; Gold Open Access
author Teh L.K.; Lee W.L.; Amir J.; Salleh M.Z.; Ismail R.
spellingShingle Teh L.K.; Lee W.L.; Amir J.; Salleh M.Z.; Ismail R.
Single step PCR for detection of allelic variation of MDR1 gene (P-glycoprotein) among three ethnic groups in Malaysia
author_facet Teh L.K.; Lee W.L.; Amir J.; Salleh M.Z.; Ismail R.
author_sort Teh L.K.; Lee W.L.; Amir J.; Salleh M.Z.; Ismail R.
title Single step PCR for detection of allelic variation of MDR1 gene (P-glycoprotein) among three ethnic groups in Malaysia
title_short Single step PCR for detection of allelic variation of MDR1 gene (P-glycoprotein) among three ethnic groups in Malaysia
title_full Single step PCR for detection of allelic variation of MDR1 gene (P-glycoprotein) among three ethnic groups in Malaysia
title_fullStr Single step PCR for detection of allelic variation of MDR1 gene (P-glycoprotein) among three ethnic groups in Malaysia
title_full_unstemmed Single step PCR for detection of allelic variation of MDR1 gene (P-glycoprotein) among three ethnic groups in Malaysia
title_sort Single step PCR for detection of allelic variation of MDR1 gene (P-glycoprotein) among three ethnic groups in Malaysia
publishDate 2007
container_title Journal of Clinical Pharmacy and Therapeutics
container_volume 32
container_issue 3
doi_str_mv 10.1111/j.1365-2710.2007.00822.x
url https://www.scopus.com/inward/record.uri?eid=2-s2.0-34247881888&doi=10.1111%2fj.1365-2710.2007.00822.x&partnerID=40&md5=72a3352b31c2f55fc8453d234d025736
description Background: P-glycoprotein (PgP) is the most extensively studied ATP-binding cassette (ABC) coded by MDR1 gene. To date, 29 single nucleotide polymorphisms (SNPs) have been identified; but only SNP C3435T has been correlated with intestinal PgP expression levels and shown to influence the absorption of orally taken drugs that are PgP substrates. Individuals homozygous for the T allele have more than fourfold lower PgP expression compared with C/C individuals. We developed a one step primer based allele specific PCR method to detect SNP at C3435T to investigate the distribution of this genotype in the local population. Method: DNA was extracted from 5 mL of whole blood using standard salting-out method. Primers were designed specific to 3′ end which amplify the variants of C3435T. The method was validated by direct DNA sequencing. Seven hundred and sixty-three healthy blood donors comprising of three major ethnic groups in Malaysia were recruited and DNA subjected to genotyping of C3435T using this method. Result: The method was found to be robust and reproducible in detecting SNP of C3435T. Interethnic variations in genotype and allele frequency were observed in PgP among the ethnic groups. In comparison to both the Caucasians and the other Asian countries, the Malay and Chinese showed a higher frequency of allele C (50-60%); while the Indian exhibits a lower frequency (40%), similar to other Indian populations. Discussion and conclusion: Using a new simple method to investigate the distribution of C3435T, we found that the allele frequency of MDR1 showed variablity between the different ethnic groups within the Malaysian population. © 2007 The Authors.
publisher
issn 13652710
language English
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accesstype All Open Access; Gold Open Access
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