Cited by 97Pharmacogenetics and Drug MetabolismGenetic Associations and EpidemiologyNutrition, Genetics, and Disease

Polymorphisms affecting gene regulation and mRNA processing: Broad implications for pharmacogenetics

JOHNSON, A, WANG, D, SADEE, W·2005·Pharmacology & Therapeutics

Abstract

Functional polymorphisms that alter gene expression and mRNA processing appear to play a critical role in shaping human phenotypic variability. Intensive studies on polymorphisms affecting drug response have revealed multiple modes of altered gene function, frequently involving cis-acting regulatory sequence variants. Experimental and in silico methods have advanced the search for such polymorphisms, but considerable challenges remain. Here, a survey of polymorphisms in drug-related genes indicates that: (a) a substantial proportion of genetic variability still remains unaccounted for; (b) a majority of these genes harbors known regulatory polymorphisms; and (c) a portion of polymorphisms affect splicing and mRNA turnover. Pharmacogenetic optimiziation of individual drug therapy may require a complete understanding of all functional sequence variants in key genes. This review surveys known noncoding polymorphisms in genes encoding cytochrome P450s and other drug-metabolizing enzymes, drug transporters, and drug targets and receptors. Current methods and challenges associated with the identification and characterization of functional polymorphisms are also discussed.

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Crossref · 10.1016/j.pharmthera.2004.11.001

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  • In prairie voles, a microsatellite in the 5' flanking region of Avpr1a containing cis-regulatory elements has functional influence over species differences and individual variation in Avpr1a expression and is associated with variation in social behavior.

    “In prairie voles, a microsatellite in the 5’ flanking region of the vasopressin receptor gene (Avpr1a) containing cis-REs has been shown to have functional influence over species differences and individual variation in Avpr1a expression and is associated with variation in social behavior (47, 48).”

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References 251 · Cited by 97

Authors
JOHNSON, A., WANG, D., & SADEE, W.
Affiliations
The Ohio State University (US)
Corresponding author
JOHNSON, A
ORCID
WANG, D
Venue
Pharmacology & Therapeutics
Publisher
Elsevier BV
Published
2005-04
Volume
106
Issue
1
Pages
19-38
ISSN
0163-7258 (ISSN-L)
OpenAlex
W2011562383
Cited by
97
References
251
Citations by year
2025: 1 · 2024: 1 · 2023: 3 · 2021: 3 · 2020: 2 · 2018: 1 · 2017: 3 · 2016: 1 · 2015: 5 · 2014: 4 · 2013: 14 · 2012: 6
FWCI
3.84
Type
journal article
Language
en
Open access
closed
Locations
  • Pharmacology & Therapeutics (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • Ohio State University
  • National Institutes of Health
  • National Institute on Drug Abuse (DA018744, R21DA018744)
Topics
  • Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmacology › Pharmacogenetics and Drug Metabolism
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Nutrition, Genetics, and Disease
Keywords
functional polymorphisms, gene expression regulation, mRNA processing, splicing, mRNA turnover, pharmacogenetics, drug response variability, cytochrome P450, drug-metabolizing enzymes, drug transporters, genetic variation
MeSH terms
Animals, Binding Sites, Biotransformation, Carrier Proteins, Cytochrome P-450 Enzyme System, Pharmaceutical Preparations, Gene Expression Regulation, Humans, Pharmacogenetics, Phenotype, Polymorphism, Genetic, RNA, Messenger

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