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一种可下调人类大电导钙依赖性钾通道的新型神经系统β亚基。

A novel nervous system beta subunit that downregulates human large conductance calcium-dependent potassium channels.

作者信息

Weiger T M, Holmqvist M H, Levitan I B, Clark F T, Sprague S, Huang W J, Ge P, Wang C, Lawson D, Jurman M E, Glucksmann M A, Silos-Santiago I, DiStefano P S, Curtis R

机构信息

Department of Biochemistry and Volen Center for Complex Systems, Brandeis University, Waltham, Massachusetts 02454, USA.

出版信息

J Neurosci. 2000 May 15;20(10):3563-70. doi: 10.1523/JNEUROSCI.20-10-03563.2000.


DOI:10.1523/JNEUROSCI.20-10-03563.2000
PMID:10804197
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6772688/
Abstract

The pore-forming alpha subunits of many ion channels are associated with auxiliary subunits that influence channel expression, targeting, and function. Several different auxiliary (beta) subunits for large conductance calcium-dependent potassium channels of the Slowpoke family have been reported, but none of these beta subunits is expressed extensively in the nervous system. We describe here the cloning and functional characterization of a novel Slowpoke beta4 auxiliary subunit in human and mouse, which exhibits only limited sequence homology with other beta subunits. This beta4 subunit coimmunoprecipitates with human and mouse Slowpoke. beta4 is expressed highly in human and monkey brain in a pattern that overlaps strikingly with Slowpoke alpha subunit, but in contrast to other Slowpoke beta subunits, it is expressed little (if at all) outside the nervous system. Also in contrast to other beta subunits, beta4 downregulates Slowpoke channel activity by shifting its activation range to more depolarized voltages and slowing its activation kinetics. beta4 may be important for the critical roles played by Slowpoke channels in the regulation of neuronal excitability and neurotransmitter release.

摘要

许多离子通道的成孔α亚基与影响通道表达、靶向定位及功能的辅助亚基相关联。据报道,Slowpoke家族的大电导钙依赖性钾通道有几种不同的辅助(β)亚基,但这些β亚基在神经系统中均未广泛表达。我们在此描述了一种新的人类和小鼠Slowpoke β4辅助亚基的克隆及功能特性,它与其他β亚基仅表现出有限的序列同源性。该β4亚基与人及小鼠的Slowpoke共同免疫沉淀。β4在人类和猴脑中高表达,其表达模式与Slowpoke α亚基显著重叠,但与其他Slowpoke β亚基不同的是,它在神经系统之外几乎不表达(若有表达也极少)。同样与其他β亚基不同的是,β4通过将其激活范围转移到更正极的电压并减慢其激活动力学,下调Slowpoke通道活性。β4对于Slowpoke通道在调节神经元兴奋性和神经递质释放中所起的关键作用可能很重要。

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本文引用的文献

[1]
Identification of the major intestinal fatty acid transport protein.

Mol Cell. 1999-9

[2]
Acute activation of Maxi-K channels (hSlo) by estradiol binding to the beta subunit.

Science. 1999-9-17

[3]
Molecular basis for the inactivation of Ca2+- and voltage-dependent BK channels in adrenal chromaffin cells and rat insulinoma tumor cells.

J Neurosci. 1999-7-1

[4]
A dynamically regulated 14-3-3, Slob, and Slowpoke potassium channel complex in Drosophila presynaptic nerve terminals.

Neuron. 1999-4

[5]
High-conductance calcium-activated potassium channels in rat brain: pharmacology, distribution, and subunit composition.

Biochemistry. 1999-4-27

[6]
Molecular basis of fast inactivation in voltage and Ca2+-activated K+ channels: a transmembrane beta-subunit homolog.

Proc Natl Acad Sci U S A. 1999-3-30

[7]
Regulation of stably expressed and native BK channels from human myometrium by cGMP- and cAMP-dependent protein kinase.

Pflugers Arch. 1998-10

[8]
Calcium-activated potassium channels.

Curr Opin Neurobiol. 1998-6

[9]
Regulation of ion channel expression by cytoplasmic subunits.

Curr Opin Neurobiol. 1998-6

[10]
The beta subunit of the high conductance calcium-activated potassium channel. Identification of residues involved in charybdotoxin binding.

J Biol Chem. 1998-6-26

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