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

被引:126
作者
Weiger, TM
Holmqvist, MH
Levitan, IB
Clark, FT
Sprague, S
Huang, WJ
Ge, P
Wang, CC
Lawson, D
Jurman, ME
Glucksmann, MA
Silos-Santiago, I
DiStefano, PS
Curtis, R
机构
[1] Brandeis Univ, Dept Biochem, Waltham, MA 02454 USA
[2] Brandeis Univ, Volen Ctr Complex Syst, Waltham, MA 02454 USA
[3] Millennium Pharmaceut, Cambridge, MA 02139 USA
[4] Salzburg Univ, Inst Zool, Dept Mol Neurobiol & Cell Physiol, A-5020 Salzburg, Austria
关键词
potassium channel; beta subunit; in situ hybridization; Slowpoke; maxi K; calcium-dependent potassium channel;
D O I
10.1523/JNEUROSCI.20-10-03563.2000
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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 beta 4 auxiliary subunit in human and mouse, which exhibits only limited sequence homology with other beta subunits. This beta 4 subunit coimmunoprecipitates with human and mouse Slowpoke. beta 4 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, beta 4 downregulates Slowpoke channel activity by shifting its activation range to more depolarized voltages and slowing its activation kinetics. beta 4 may be important for the critical roles played by Slowpoke channels in the regulation of neuronal excitability and neurotransmitter release.
引用
收藏
页码:3563 / 3570
页数:8
相关论文
共 40 条
[1]   CALCIUM-ACTIVATED POTASSIUM CHANNELS EXPRESSED FROM CLONED COMPLEMENTARY DNAS [J].
ADELMAN, JP ;
SHEN, KZ ;
KAVANAUGH, MP ;
WARREN, RA ;
WU, YN ;
LAGRUTTA, A ;
BOND, CT ;
NORTH, RA .
NEURON, 1992, 9 (02) :209-216
[2]   PHOSPHORYLATION AND DEPHOSPHORYLATION MODULATE A CA2+-ACTIVATED K+ CHANNEL IN RAT PEPTIDERGIC NERVE-TERMINALS [J].
BIELEFELDT, K ;
JACKSON, MB .
JOURNAL OF PHYSIOLOGY-LONDON, 1994, 475 (02) :241-254
[3]   MSLO, A COMPLEX MOUSE GENE ENCODING MAXI CALCIUM-ACTIVATED POTASSIUM CHANNELS [J].
BUTLER, A ;
TSUNODA, S ;
MCCOBB, DP ;
WEI, A ;
SALKOFF, L .
SCIENCE, 1993, 261 (5118) :221-224
[4]   EXOCYTOTIC CA2+ CHANNELS IN MAMMALIAN CENTRAL NEURONS [J].
DUNLAP, K ;
LUEBKE, JI ;
TURNER, TJ .
TRENDS IN NEUROSCIENCES, 1995, 18 (02) :89-98
[5]  
Dworetzky SI, 1996, J NEUROSCI, V16, P4543
[6]   CLONING AND EXPRESSION OF A HUMAN LARGE-CONDUCTANCE CALCIUM-ACTIVATED POTASSIUM CHANNEL [J].
DWORETZKY, SI ;
TROJNACKI, JT ;
GRIBKOFF, VK .
MOLECULAR BRAIN RESEARCH, 1994, 27 (01) :189-193
[7]  
GARCIACALVO M, 1994, J BIOL CHEM, V269, P676
[8]  
GHO M, 1992, J EXP BIOL, V170, P93
[9]   The β subunit of the high conductance calcium-activated potassium channel -: Identification of residues involved in charybdotoxin binding [J].
Hanner, M ;
Vianna-Jorge, R ;
Kamassah, A ;
Schmalhofer, WA ;
Knaus, HG ;
Kaczorowski, GJ ;
Garcia, ML .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (26) :16289-16296
[10]   Ca2+-dependent inactivation of large conductance Ca2+-activated K+ (BK) channels in rat hippocampal neurones produced by pore block from an associated particle [J].
Hicks, GA ;
Marrion, NV .
JOURNAL OF PHYSIOLOGY-LONDON, 1998, 508 (03) :721-734