Molecular Diversity of K+ Channels
Abstract
ABSTRACT: K+ channel principal subunits are by far the largest and most diverse of the ion channels. This diversity originates partly from the large number of genes coding for K+ channel principal subunits, but also from other processes such as alternative splicing, generating multiple mRNA transcripts from a single gene, heteromeric assembly of different principal subunits, as well as possible RNA editing and posttranslational modifications. In this chapter, we attempt to give an overview (mostly in tabular format) of the different genes coding for K+ channel principal and accessory subunits and their genealogical relationships. We discuss the possible correlation of different principal subunits with native K+ channels, the biophysical and pharmacological properties of channels formed when principal subunits are expressed in heterologous expression systems, and their patterns of tissue expression. In addition, we devote a section to describing how diversity of K+ channels can be conferred by heteromultimer formation, accessory subunits, alternative splicing, RNA editing and posttranslational modifications. We trust that this collection of facts will be of use to those attempting to compare the properties of new subunits to the properties of others already known or to those interested in a comparison between native channels and cloned candidates.
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Kv3 channels have a 10-50 mV higher activation threshold than any other known mammalian voltage-gated K+ channels.
“The Kv3 channels have a 10-50 mV higher activation threshold than any other known mammalian voltage-gated K+ channels (Coetzee et al., 1999).”
From Overexpressing low‐density lipoprotein receptor reduces tau‐associated neurodegeneration in relation to apoE‐linked mechanisms (2021) · cites this paper as Coetzee et al., 1999
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- Authors
- COETZEE, W. A., AMARILLO, Y., CHIU, J., CHOW, A., LAU, D., McCORMACK, T., MORENA, H., NADAL, M. S., OZAITA, A., POUNTNEY, D., SAGANICH, M., DE MIERA, E. V., & RUDY, B.
- Affiliations
- NYU Langone Health (US)
- New York University (US)
- Corresponding author
- COETZEE, WILLIAM A.
- Venue
- Annals of the New York Academy of Sciences
- Publisher
- Wiley
- Published
- 1999-04
- Volume
- 868
- Issue
- 1
- Pages
- 233-255
- ISSN
- 0077-8923 (ISSN-L)
- 1749-6632
- OpenAlex
- W2099587101
- Cited by
- 1,095
- References
- 1
- Citations by year
- 2026: 5 · 2025: 19 · 2024: 19 · 2023: 15 · 2022: 20 · 2021: 31 · 2020: 29 · 2019: 27 · 2018: 25 · 2017: 22 · 2016: 30 · 2015: 35 · 2014: 50 · 2013: 44 · 2012: 41
- FWCI
- 4.16
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Annals of the New York Academy of Sciences (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ion channel regulation and function
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiac electrophysiology and arrhythmias
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ion Transport and Channel Regulation
- Keywords
- potassium channels, potassium channel subunits, molecular diversity, alternative splicing, auxiliary subunits, RNA editing, post-translational modification, genealogy, tissue expression, channel pharmacology, heterologous expression
- MeSH terms
- Animals, Cloning, Molecular, Gene Expression Regulation, Humans, Phylogeny, Protein Conformation, Protein Processing, Post-Translational, RNA, Messenger, Xenopus, Potassium Channels, Ion Channel Gating, RNA Editing, Alternative Splicing
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