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Complex Promoter and Coding Region β 2-adrenergic Receptor Haplotypes Alter Receptor Expression and Predict in vivo Responsiveness

Connie M. Drysdale, Dennis W. McGraw, Catharine B. Stack, J. Claiborne Stephens, Richard S. Judson, Krishnan Nandabalan, Kevin Arnold, Gualberto Ruano and Stephen B. Liggett
Proceedings of the National Academy of Sciences of the United States of America
Vol. 97, No. 19 (Sep. 12, 2000), pp. 10483-10488
Stable URL: http://www.jstor.org/stable/123587
Page Count: 6
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Since scans are not currently available to screen readers, please contact JSTOR User Support for access. We'll provide a PDF copy for your screen reader.
Complex Promoter and Coding Region β 2-adrenergic Receptor Haplotypes Alter Receptor Expression and Predict in vivo Responsiveness
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Abstract

The human β 2-adrenergic receptor gene has multiple single-nucleotide polymorphisms (SNPs), but the relevance of chromosomally phased SNPs (haplotypes) is not known. The phylogeny and the in vitro and in vivo consequences of variations in the 5′ upstream and ORF were delineated in a multiethnic reference population and an asthmatic cohort. Thirteen SNPs were found organized into 12 haplotypes out of the theoretically possible 8,192 combinations. Deep divergence in the distribution of some haplotypes was noted in Caucasian, African-American, Asian, and Hispanic-Latino ethnic groups with >20-fold differences among the frequencies of the four major haplotypes. The relevance of the five most common β 2-adrenergic receptor haplotype pairs was determined in vivo by assessing the bronchodilator response to β agonist in asthmatics. Mean responses by haplotype pair varied by >2-fold, and response was significantly related to the haplotype pair (P = 0.007) but not to individual SNPs. Expression vectors representing two of the haplotypes differing at eight of the SNP loci and associated with divergent in vivo responsiveness to agonist were used to transfect HEK293 cells. β 2-adrenergic receptor mRNA levels and receptor density in cells transfected with the haplotype associated with the greater physiologic response were ≈ 50% greater than those transfected with the lower response haplotype. The results indicate that the unique interactions of multiple SNPs within a haplotype ultimately can affect biologic and therapeutic phenotype and that individual SNPs may have poor predictive power as pharmacogenetic loci.

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