Literature DB >> 12944270

KCNE4 is an inhibitory subunit to Kv1.1 and Kv1.3 potassium channels.

Morten Grunnet1, Hannne B Rasmussen, Anders Hay-Schmidt, Maiken Rosenstierne, Dan A Klaerke, Søren-Peter Olesen, Thomas Jespersen.   

Abstract

Kv1 potassium channels are widely distributed in mammalian tissues and are involved in a variety of functions from controlling the firing rate of neurons to maturation of T-lymphocytes. Here we show that the newly described KCNE4 beta-subunit has a drastic inhibitory effect on currents generated by Kv1.1 and Kv1.3 potassium channels. The inhibition is found on channels expressed heterologously in both Xenopus oocytes and mammalian HEK293 cells. mKCNE4 does not inhibit Kv1.2, Kv1.4, Kv1.5, or Kv4.3 homomeric complexes, but it does significantly reduce current through Kv1.1/Kv1.2 and Kv1.2/Kv1.3 heteromeric complexes. Confocal microscopy and Western blotting reveal that Kv1.1 is present at the cell surface together with KCNE4. Real-time RT-PCR shows a relatively high presence of mKCNE4 mRNA in several organs, including uterus, kidney, lung, intestine, and in embryo, whereas a much lower mRNA level is detected in the heart and in five different parts of the brain. Having the broad distribution of Kv1 channels in mind, the demonstrated inhibitory property of KCNE4-subunits could locally and/or transiently have a dramatic influence on cellular excitability and on setting resting membrane potentials.

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Year:  2003        PMID: 12944270      PMCID: PMC1303329          DOI: 10.1016/S0006-3495(03)74585-8

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  64 in total

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Journal:  Ann N Y Acad Sci       Date:  1999-04-30       Impact factor: 5.691

2.  Complex subunit assembly of neuronal voltage-gated K+ channels. Basis for high-affinity toxin interactions and pharmacology.

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Journal:  J Biol Chem       Date:  1997-10-31       Impact factor: 5.157

3.  The conduction pore of a cardiac potassium channel.

Authors:  K K Tai; S A Goldstein
Journal:  Nature       Date:  1998-02-05       Impact factor: 49.962

4.  Pathophysiological mechanisms of dominant and recessive KVLQT1 K+ channel mutations found in inherited cardiac arrhythmias.

Authors:  B Wollnik; B C Schroeder; C Kubisch; H D Esperer; P Wieacker; T J Jentsch
Journal:  Hum Mol Genet       Date:  1997-10       Impact factor: 6.150

5.  Genomic organization, chromosomal localization, tissue distribution, and biophysical characterization of a novel mammalian Shaker-related voltage-gated potassium channel, Kv1.7.

Authors:  K Kalman; A Nguyen; J Tseng-Crank; I D Dukes; G Chandy; C M Hustad; N G Copeland; N A Jenkins; H Mohrenweiser; B Brandriff; M Cahalan; G A Gutman; K G Chandy
Journal:  J Biol Chem       Date:  1998-03-06       Impact factor: 5.157

6.  MiRP1 forms IKr potassium channels with HERG and is associated with cardiac arrhythmia.

Authors:  G W Abbott; F Sesti; I Splawski; M E Buck; M H Lehmann; K W Timothy; M T Keating; S A Goldstein
Journal:  Cell       Date:  1999-04-16       Impact factor: 41.582

7.  Subunit composition of brain voltage-gated potassium channels determined by hongotoxin-1, a novel peptide derived from Centruroides limbatus venom.

Authors:  A Koschak; R M Bugianesi; J Mitterdorfer; G J Kaczorowski; M L Garcia; H G Knaus
Journal:  J Biol Chem       Date:  1998-01-30       Impact factor: 5.157

8.  Mutations in the hminK gene cause long QT syndrome and suppress IKs function.

Authors:  I Splawski; M Tristani-Firouzi; M H Lehmann; M C Sanguinetti; M T Keating
Journal:  Nat Genet       Date:  1997-11       Impact factor: 38.330

9.  Coexpression of the KCNA3B gene product with Kv1.5 leads to a novel A-type potassium channel.

Authors:  T Leicher; R Bähring; D Isbrandt; O Pongs
Journal:  J Biol Chem       Date:  1998-12-25       Impact factor: 5.157

10.  KCNE1-like gene is deleted in AMME contiguous gene syndrome: identification and characterization of the human and mouse homologs.

Authors:  M Piccini; F Vitelli; M Seri; L J Galietta; O Moran; A Bulfone; S Banfi; B Pober; A Renieri
Journal:  Genomics       Date:  1999-09-15       Impact factor: 5.736

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  27 in total

1.  Structural models for the KCNQ1 voltage-gated potassium channel.

Authors:  Jarrod A Smith; Carlos G Vanoye; Alfred L George; Jens Meiler; Charles R Sanders
Journal:  Biochemistry       Date:  2007-11-14       Impact factor: 3.162

2.  MiRP3 acts as an accessory subunit with the BK potassium channel.

Authors:  Daniel I Levy; Sherry Wanderling; Daniel Biemesderfer; Steve A N Goldstein
Journal:  Am J Physiol Renal Physiol       Date:  2008-05-07

3.  Novel exon 1 protein-coding regions N-terminally extend human KCNE3 and KCNE4.

Authors:  Geoffrey W Abbott
Journal:  FASEB J       Date:  2016-05-09       Impact factor: 5.191

4.  KCNE gene expression is dependent on the proliferation and mode of activation of leukocytes.

Authors:  Laura Solé; Albert Vallejo-Gracia; Sara R Roig; Antonio Serrano-Albarrás; Laura Marruecos; Joan Manils; Diana Gómez; Concepció Soler; Antonio Felipe
Journal:  Channels (Austin)       Date:  2013-01-17       Impact factor: 2.581

5.  Genetic perturbations suggest a role of the resting potential in regulating the expression of the ion channels of the KCNA and HCN families in octopus cells of the ventral cochlear nucleus.

Authors:  Xiao-Jie Cao; Donata Oertel
Journal:  Hear Res       Date:  2017-01-05       Impact factor: 3.208

Review 6.  KCNE4 and KCNE5: K(+) channel regulation and cardiac arrhythmogenesis.

Authors:  Geoffrey W Abbott
Journal:  Gene       Date:  2016-07-30       Impact factor: 3.688

7.  Kcne4 deletion sex- and age-specifically impairs cardiac repolarization in mice.

Authors:  Shawn M Crump; Zhaoyang Hu; Ritu Kant; Daniel I Levy; Steve A N Goldstein; Geoffrey W Abbott
Journal:  FASEB J       Date:  2015-09-23       Impact factor: 5.191

8.  KCNE3 truncation mutants reveal a bipartite modulation of KCNQ1 K+ channels.

Authors:  Steven D Gage; William R Kobertz
Journal:  J Gen Physiol       Date:  2004-12       Impact factor: 4.086

9.  Transgenic system for conditional induction and rescue of chronic myocardial hibernation provides insights into genomic programs of hibernation.

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Journal:  Proc Natl Acad Sci U S A       Date:  2007-12-27       Impact factor: 11.205

10.  KCNE1 and KCNE3 beta-subunits regulate membrane surface expression of Kv12.2 K(+) channels in vitro and form a tripartite complex in vivo.

Authors:  Sinead M Clancy; Bihan Chen; Federica Bertaso; Julien Mamet; Timothy Jegla
Journal:  PLoS One       Date:  2009-07-22       Impact factor: 3.240

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