A functional polymorphism of the Gαq (GNAQ) gene is associated with accelerated mortality in African-American heart failure

Stephen B. Liggett, Reagan J. Kelly, Rohan R. Parekh, Scot J. Matkovich, Bonnie J. Benner, Harvey S. Hahn, Faisal M. Syed, Anita S. Galvez, Karen L. Case, Nancy Mcguire, Amy M. Odley, Li Sparks, Sharon L.R. Kardia, Gerald W. Dorn

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18 Scopus citations

Abstract

Gαq, encoded by the human GNAQ gene, is an effector subunit of the Gq heterotrimeric G-protein and the convergence point for signaling of multiple Gq-coupled neurohormonal receptors. To identify naturally occurring mutations that could modify GNAQ transcription, we examined genomic DNA isolated from 355 normal subjects for genetic variants in transcription factor binding motifs. Of seven variants identified, the most common was a GC to TT dinucleotide substitution at -694/-695 (allele frequency of 0.467 in Caucasians and 0.329 in African Americans) within a GC-rich domain containing consensus binding sites for Sp-1, c-rel and EGR-1. In promoter-reporter analyses, the TT substitution increased promoter activity in cultured neonatal rat cardiac myocytes and human HEK fibroblasts by ∼30% at baseline and after stimulation with phorbol ester. Two other relatively common polymorphisms, -173G/A and -168G/A, did not affect promoter activity. Since altered expression/ activity of Gαq is implicated in heart disease, we re-sequenced the GNAQ promoter in 1052 prospectively followed heart failure patients. The TT variant was not increased in heart failure, but was associated with decreased survival time among African Americans, with an adjusted RR of death/cardiac transplant of 1.95 (95% CI % 1.21-3.13) for heterozygotes and 2.4 (95% CI = 1.36-4.26) for homozygotes. Gel mobility shift assays showed that this GC/TT substitution eliminated Sp-1 binding without affecting c-rel or EGR-1 binding to this promoter fragment. Thus, the GNAQ -694/-695 promoter polymorphism alters transcription factor binding, increases promoter activity and adversely affects outcome in human heart failure.

Original languageEnglish
Pages (from-to)2740-2750
Number of pages11
JournalHuman molecular genetics
Volume16
Issue number22
DOIs
StatePublished - Nov 15 2007
Externally publishedYes

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    Liggett, S. B., Kelly, R. J., Parekh, R. R., Matkovich, S. J., Benner, B. J., Hahn, H. S., Syed, F. M., Galvez, A. S., Case, K. L., Mcguire, N., Odley, A. M., Sparks, L., Kardia, S. L. R., & Dorn, G. W. (2007). A functional polymorphism of the Gαq (GNAQ) gene is associated with accelerated mortality in African-American heart failure. Human molecular genetics, 16(22), 2740-2750. https://doi.org/10.1093/hmg/ddm229