Kv10.1, the voltage-gated non-inactivating delayed rectifier potassium channel, is overexpressed in variety of cancer cells and is involved in oncogenesis and tumor progression. Its splice variants E65 and E70, which were discovered in melanoma cell lines, have no conducting abilities but may
physically interact with Kv10.1 and thereby regulate its function. Here, we investigated possible influence of E65 and E70 on electrophysiological properties of Kv10.1. Analysis of current-voltage relationships revealed a dose-dependent reduction of Kv10.1 current mediated by both splice
variants. The channel demonstrated characteristic feature of activation kinetics, a Cole-Moore shift, irrespective of the isoforms presence. Both E65 and E70 were able to increase the rise time after -60 mV conditioning when expressed at 1:10 ratio with full length channel. Co-expression of E65 or
E70 with Kv1.4 did not resulted in considerable changes in channel activity; therefore interactions of splice variants with Kv10.1 are likely to be specific. Downregulation of Kv10.1 activity by E65 and E70 splice variants may modulate tumorigenesis and be associated with less aggressive forms
of cancer.
Inhaltsverzeichnis (Table of Contents)
- Abstract
- Introduction
- Materials and Methods
- Results
- Discussion
- References
Zielsetzung und Themenschwerpunkte (Objectives and Key Themes)
This project aimed to examine the impact of E65 and E70 splice variants on the electrophysiological properties of the Kv10.1 channel, specifically focusing on dose-dependence and the specificity of their effects.
- The role of Kv10.1 in cancer development and progression.
- The influence of E65 and E70 splice variants on Kv10.1 channel activity.
- The potential of splice variants to modulate tumorigenesis.
- The electrophysiological properties of Kv10.1 channel.
- The mechanisms of interaction between Kv10.1 and its splice isoforms.
Zusammenfassung der Kapitel (Chapter Summaries)
- Abstract: This section provides a concise overview of the research project, outlining the key findings and their potential implications. It highlights the role of Kv10.1 in cancer and the potential of its splice variants E65 and E70 to modulate tumorigenesis.
- Introduction: This chapter introduces the background information on Kv10.1, its role in cancer development, and the potential of its splice variants to influence channel function. It discusses the structural features of Kv10.1, its regulation, and the significance of alternative splicing in its activity.
- Materials and Methods: This chapter details the experimental methods used in the study, including cell culture techniques, molecular cloning, and electrophysiological recordings.
- Results: This chapter presents the experimental results obtained, including the effects of E65 and E70 splice variants on the electrophysiological properties of Kv10.1. It analyzes the dose-dependence of these effects and investigates the specificity of their interactions with Kv10.1.
Schlüsselwörter (Keywords)
The primary keywords and focus topics of this research include Kv10.1, E65, E70, splice variants, electrophysiology, cancer, tumorigenesis, voltage-gated potassium channels, ion channels, and alternative splicing. These terms represent the core concepts and research focus of this project.
- Quote paper
- Maryna Psol (Author), Vincenzo Romaniello (Author), 2013, Effect of E65 and E70 splice isoforms on electrophysiological properties of Kv10.1, Munich, GRIN Verlag, https://www.grin.com/document/263279
