Kv1.5 potassium channel gene regulation by Sp1 transcription factor and oxidative stress

Fountain, Samuel J. ORCID: https://orcid.org/0000-0002-6028-0548, Cheong, Alex, Li, Jing, Dondas, Naciye Y., Zeng, Fanning, Wood, Ian C. and Beech, David J. (2007) Kv1.5 potassium channel gene regulation by Sp1 transcription factor and oxidative stress. AJP - Heart and Circulatory Physiology, 293 (5). pp. 2719-2725.

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KV1.5, a voltage-gated potassium channel, has functional importance in regulating blood vessel tone and cardiac action potentials and is a target for numerous therapeutic drug development programs. Despite the importance of KV1.5, there is little knowledge of the mechanisms controlling expression of its underlying gene, Kcna5. We identified a 5' flanking region of the murine Kcna5 gene that drives expression of a luciferase reporter gene in primary smooth muscle cells and a smooth muscle cell line. The promoter contained CACCC nucleotide motifs, which we have shown to bind the Sp1 transcription factor in the aorta under physiological conditions in vivo. Inhibition of Sp1-Kcna5 promoter interactions using mithramycin A, a dominant-negative Sp1 mutant, or disruption of the CACCC boxes by mutagenesis inhibited promoter activity. Conversely, expression of exogenous Sp1 augmented promoter activity. Sp1 has known sensitivity to oxidative stress and, consistent with this property, Kcna5 promoter activity was suppressed by hydrogen peroxide-induced oxidative stress. Our results show that Kcna5 promoter activity in vascular smooth muscle is critically dependent on Sp1 regulation via CACCC box motifs and identify mechanisms that potentially influence the expression of KV1.5 channel expression in physiological or pathological conditions.

Item Type: Article
Faculty \ School: Faculty of Science > School of Biological Sciences
UEA Research Groups: Faculty of Science > Research Groups > Cells and Tissues
Depositing User: Vishal Gautam
Date Deposited: 19 Jan 2011 16:24
Last Modified: 22 Apr 2023 01:11
URI: https://ueaeprints.uea.ac.uk/id/eprint/19419
DOI: 10.1152/ajpheart.00637.2007

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