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PMID: 10766764 Published · ppublish English Journal Article

Cloning and functional expression of two families of beta-subunits of the large conductance calcium-activated K+ channel.

The Journal of biological chemistry ·Vol. 275 ·No. 30 ·2000-07-28 ·Pages 23211-8

Uebele VN, Lagrutta A, Wade T, Figueroa DJ, Liu Y, McKenna E, Austin CP, Bennett PB, Swanson R

Abstract

We report here a characterization of two families of calcium-activated K(+) channel beta-subunits, beta2 and beta3, which are encoded by distinct genes that map to 3q26.2-27. A single beta2 family member and four alternatively spliced variants of beta3 were investigated. These subunits have predicted molecular masses of 27. 1-31.6 kDa, share approximately 30-44% amino acid identity with beta1, and exhibit distinct but overlapping expression patterns. Coexpression of the beta2 or beta3a-c subunits with a BK alpha-subunit altered the functional properties of the current expressed by the alpha-subunit alone. The beta2 subunit rapidly and completely inactivated the current and shifted the voltage dependence for activation to more polarized membrane potentials. In contrast, coexpression of the beta3a-c subunits resulted in only partial inactivation of the current, and the beta3b subunit conferred an apparent inward rectification. Furthermore, unlike the beta1 and beta2 subunits, none of the beta3 subunits increased channel sensitivity to calcium or voltage. The tissue-specific expression of these beta-subunits may allow for the assembly of a large number of distinct BK channels in vivo, contributing to the functional diversity of native BK currents.

MeSH Terms
Alternative Splicing Amino Acid Sequence Calcium/metabolism Chromosome Mapping Chromosomes, Human, Pair 3 Cloning, Molecular DNA, Complementary Humans In Situ Hybridization, Fluorescence Molecular Sequence Data Potassium Channels/chemistry,genetics,metabolism Sequence Homology, Amino Acid
Chemicals
DNA, Complementary Potassium Channels Calcium
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Uebele V N
Merck Research Laboratories, West Point, Pennsylvania 19486, USA. victor_uebele@merck.com
Lagrutta A
Wade T
Figueroa D J
Liu Y
McKenna E
Austin C P
Bennett P B
Swanson R
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
2000-07-28
Pages
23211-8
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Databases
GENBANK
AF204159, AF204160, AF204161, AF204162
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