Am J Physiol Cell Physiol AJP: Heart and Circulatory Physiology
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Am J Physiol Cell Physiol 296: C498-C504, 2009. First published December 24, 2008; doi:10.1152/ajpcell.00462.2008
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METHODS IN CELL PHYSIOLOGY

Molecular beacons can assess changes in expression and 3'-polyadenylation of human eNOS mRNA

Rachel Jones,1 Meredith B. Baker,1 Martina Weber,1 David G. Harrison,1 Gang Bao,2,* and Charles D. Searles1,*

1Division of Cardiology, Emory University School of Medicine, Atlanta, Georgia; and 2Department of Biomedical Engineering, Georgia Institute of Technology and Emory University, Atlanta, Georgia

Submitted 8 September 2008 ; accepted in final form 15 December 2008

The endothelium plays an essential role in maintaining vascular homeostasis, and it fulfills this role by modulating intracellular signaling and gene expression in response to chemical and mechanical stimuli. Assessing changes in endothelial gene expression is essential to understanding how physiological and pathophysiological processes modulate vascular homeostasis. Here we describe the use of molecular beacons to rapidly and quantitatively assess expression and 3'-polyadenylation of a gene that is important for vascular homeostasis, endothelial nitric oxide synthase (eNOS). Single- and dual-fluorescence resonance energy transfer (FRET) molecular beacon hybridization assays were developed to measure changes in mRNA levels and 3'-polyadenylation, respectively, in primary human endothelial cell cultures subjected to laminar shear stress or statin treatment. Optimized beacon hybridization assays took ~15 min to perform, and eNOS mRNA levels were validated by quantitative real-time RT-PCR. Competitive inhibition assays and posttranscriptional silencing of eNOS expression were used to verify the specificity of molecular beacon fluorescence. Finally, the dual-FRET method was used to assess eNOS polyadenylation in tissues isolated from mice subjected to exercise training. These data demonstrate that molecular beacons can be used to rapidly and efficiently measure endothelial gene expression and 3'-polyadenylation. This approach could easily be adapted for studies of other endothelial genes and has promise for applications in live endothelial cells.

endothelial nitric oxide synthase; gene expression; dual-fluorescence resonance energy transfer



Address for reprint requests and other correspondence: C. Searles, Div. of Cardiology, Emory Univ. School of Medicine, Atlanta, GA 30322 (e-mail: csearle{at}emory.edu); G. Bao, Dept. of Biomedical Engineering, Georgia Inst. of Technology and Emory Univ., Atlanta, GA 30322 (e-mail: gang.bao{at}bme.gatech.edu)







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