Literature DB >> 18698231

Polymorphisms affecting gene transcription and mRNA processing in pharmacogenetic candidate genes: detection through allelic expression imbalance in human target tissues.

Andrew D Johnson1, Ying Zhang, Audrey C Papp, Julia K Pinsonneault, Jeong-Eun Lim, David Saffen, Zunyan Dai, Danxin Wang, Wolfgang Sadée.   

Abstract

BACKGROUND: Genetic variation in mRNA expression plays a critical role in human phenotypic diversity, but it has proven difficult to detect regulatory polymorphisms - mostly single nucleotide polymorphisms (rSNPs). Additionally, variants in the transcribed region, termed here 'structural RNA SNPs' (srSNPs), can affect mRNA processing and turnover. Both rSNPs and srSNPs cause allelic mRNA expression imbalance (AEI) in heterozygous individuals. We have used AEI to discover and characterize regulatory polymorphisms in OPRM1, TPH2, MDR1, DRD2, and VKORC1. The objective of this study was to use AEI to determine the extent of cis-regulatory factors in pharmacogenetic genes.
METHODS: We applied a rapid and accurate AEI methodology for testing 42 genes implicated in cardiovascular and central nervous system diseases, and affecting drug metabolism and transport. Each gene was analyzed in physiologically relevant human autopsy tissues, including brain, heart, liver, intestines, and lymphocytes.
RESULTS: Substantial AEI was observed in approximately 55% of the surveyed genes. Focusing on cardiovascular candidate genes in human hearts, AEI analysis revealed frequent cis-acting regulatory factors in ACE and SOD2 mRNA expression, having potential clinical significance. SNP scanning to locate regulatory polymorphisms in a number of genes failed to support several previously proposed promoter SNPs discovered with use of reporter gene assays in heterologous tissues, while srSNPs appear more frequent than expected. Computational analysis of mRNA folding indicates that approximately 90% of srSNPs affect mRNA folding, and hence potentially function.
CONCLUSION: Our results indicate that both rSNPs and srSNPs represent a still largely untapped reservoir of variants that contribute to human phenotypic diversity.

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Year:  2008        PMID: 18698231      PMCID: PMC2779843          DOI: 10.1097/FPC.0b013e3283050107

Source DB:  PubMed          Journal:  Pharmacogenet Genomics        ISSN: 1744-6872            Impact factor:   2.089


  51 in total

1.  In vivo characterization of regulatory polymorphisms by allele-specific quantification of RNA polymerase loading.

Authors:  Julian C Knight; Brendan J Keating; Kirk A Rockett; Dominic P Kwiatkowski
Journal:  Nat Genet       Date:  2003-03-10       Impact factor: 38.330

2.  Detection of regulatory variation in mouse genes.

Authors:  Christopher R Cowles; Joel N Hirschhorn; David Altshuler; Eric S Lander
Journal:  Nat Genet       Date:  2002-10-15       Impact factor: 38.330

3.  Allelic variation in human gene expression.

Authors:  Hai Yan; Weishi Yuan; Victor E Velculescu; Bert Vogelstein; Kenneth W Kinzler
Journal:  Science       Date:  2002-08-16       Impact factor: 47.728

4.  Natural variation in human gene expression assessed in lymphoblastoid cells.

Authors:  Vivian G Cheung; Laura K Conlin; Teresa M Weber; Melissa Arcaro; Kuang-Yu Jen; Michael Morley; Richard S Spielman
Journal:  Nat Genet       Date:  2003-02-03       Impact factor: 38.330

5.  Abundant raw material for cis-regulatory evolution in humans.

Authors:  Matthew V Rockman; Gregory A Wray
Journal:  Mol Biol Evol       Date:  2002-11       Impact factor: 16.240

6.  The cyclin D1 alternative transcripts [a] and [b] are expressed in normal and malignant lymphocytes and their relative levels are influenced by the polymorphism at codon 241.

Authors:  D Howe; C Lynas
Journal:  Haematologica       Date:  2001-06       Impact factor: 9.941

7.  Polymorphisms in the SOD2 and HLA-DRB1 genes are associated with nonfamilial idiopathic dilated cardiomyopathy in Japanese.

Authors:  S Hiroi; H Harada; H Nishi; M Satoh; R Nagai; A Kimura
Journal:  Biochem Biophys Res Commun       Date:  1999-08-02       Impact factor: 3.575

8.  Decreased expression of manganese superoxide dismutase in transformed cells is associated with increased cytosine methylation of the SOD2 gene.

Authors:  Y Huang; T He; F E Domann
Journal:  DNA Cell Biol       Date:  1999-08       Impact factor: 3.311

9.  Synonymous mutations in the human dopamine receptor D2 (DRD2) affect mRNA stability and synthesis of the receptor.

Authors:  Jubao Duan; Mark S Wainwright; Josep M Comeron; Naruya Saitou; Alan R Sanders; Joel Gelernter; Pablo V Gejman
Journal:  Hum Mol Genet       Date:  2003-02-01       Impact factor: 6.150

10.  PKA-dependent binding of mRNA to the mitochondrial AKAP121 protein.

Authors:  Michael D Ginsberg; Antonio Feliciello; Jeffrey K Jones; Enrico V Avvedimento; Max E Gottesman
Journal:  J Mol Biol       Date:  2003-04-04       Impact factor: 5.469

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  49 in total

Review 1.  Pharmacogenomics of the RNA world: structural RNA polymorphisms in drug therapy.

Authors:  W Sadee; D Wang; A C Papp; J K Pinsonneault; R M Smith; R A Moyer; A D Johnson
Journal:  Clin Pharmacol Ther       Date:  2011-02-02       Impact factor: 6.875

2.  Drug therapy and personalized health care: pharmacogenomics in perspective.

Authors:  Wolfgang Sadee
Journal:  Pharm Res       Date:  2008-08-26       Impact factor: 4.200

3.  Targeted screening of cis-regulatory variation in human haplotypes.

Authors:  Dominique J Verlaan; Bing Ge; Elin Grundberg; Rose Hoberman; Kevin C L Lam; Vonda Koka; Joana Dias; Scott Gurd; Nicolas W Martin; Hans Mallmin; Olof Nilsson; Eef Harmsen; Ken Dewar; Tony Kwan; Tomi Pastinen
Journal:  Genome Res       Date:  2008-10-29       Impact factor: 9.043

4.  Genetic associations with expression for genes implicated in GWAS studies for atherosclerotic cardiovascular disease and blood phenotypes.

Authors:  Xiaoling Zhang; Andrew D Johnson; Audrey E Hendricks; Shih-Jen Hwang; Kahraman Tanriverdi; Santhi K Ganesh; Nicholas L Smith; Patricia A Peyser; Jane E Freedman; Christopher J O'Donnell
Journal:  Hum Mol Genet       Date:  2013-09-20       Impact factor: 6.150

Review 5.  Pharmacogenomic discovery using cell-based models.

Authors:  Marleen Welsh; Lara Mangravite; Marisa Wong Medina; Kelan Tantisira; Wei Zhang; R Stephanie Huang; Howard McLeod; M Eileen Dolan
Journal:  Pharmacol Rev       Date:  2009-12       Impact factor: 25.468

6.  Allelic imbalance (AI) identifies novel tissue-specific cis-regulatory variation for human UGT2B15.

Authors:  Chang Sun; Catherine Southard; David B Witonsky; Olufunmilayo I Olopade; Anna Di Rienzo
Journal:  Hum Mutat       Date:  2010-01       Impact factor: 4.878

7.  Association of OPRM1 A118G variant with risk of morphine-induced respiratory depression following spine fusion in adolescents.

Authors:  V Chidambaran; J Mavi; H Esslinger; V Pilipenko; L J Martin; K Zhang; S Sadhasivam
Journal:  Pharmacogenomics J       Date:  2014-09-30       Impact factor: 3.550

Review 8.  OPRM1 SNP (A118G): involvement in disease development, treatment response, and animal models.

Authors:  Stephen D Mague; Julie A Blendy
Journal:  Drug Alcohol Depend       Date:  2010-01-13       Impact factor: 4.492

9.  Polymorphisms of dopamine receptor genes and risk of visual hallucinations in Parkinson's patients.

Authors:  M Ferrari; C Comi; F Marino; L Magistrelli; F De Marchi; R Cantello; G Riboldazzi; G Bono; M Cosentino
Journal:  Eur J Clin Pharmacol       Date:  2016-08-06       Impact factor: 2.953

10.  Genetic association of GABA-A receptor alpha-2 and mu opioid receptor with cocaine cue-reactivity: evidence for inhibitory synaptic neurotransmission involvement in cocaine dependence.

Authors:  David Smelson; Lei Yu; Steven Buyske; Gerardo Gonzalez; Jay Tischfield; Curtis K Deutsch; Douglas Ziedonis
Journal:  Am J Addict       Date:  2012 Sep-Oct
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