Literature DB >> 10729221

Gene structures and expression profiles of three human KCND (Kv4) potassium channels mediating A-type currents I(TO) and I(SA).

D Isbrandt1, T Leicher, R Waldschütz, X Zhu, U Luhmann, U Michel, K Sauter, O Pongs.   

Abstract

The four known members of the KCND/Kv4 channel family encode voltage-gated potassium channels. Recent studies provide evidence that members of the Kv4 channel family are responsible for native, rapidly inactivating (A-type) currents described in heart (I(TO)) and neurons (I(SA)). In this study, we cloned the human KCND1 cDNA, localized the KCND1 gene to chromosome Xp11.23-p11.3, and determined the genomic structure and tissue-specific expression of the KCND1, KCND2, and KCND3 genes, respectively. The open reading frame of Kv4. 1 is 1941 nucleotides long, predicting a protein of 647 amino acids. The deduced protein sequence of Kv4.1 shows an overall identity of 60% with Kv4.2 and Kv4.3L and corresponds to the common structure of voltage-gated potassium channels. KCND1-specific transcripts were detectable in human brain, heart, liver, kidney, thyroid gland, and pancreas, as revealed by Northern blot and RT-PCR experiments. The comparison of the expression patterns of the known Kv4 family members shows subtype specificity with significant overlaps. The KCND gene structures exhibit an evolutionarily conserved exon pattern with a large first exon containing the intracellular N-terminus and the putative membrane-spanning regions S1 to S5, as well as part of the pore region. The KCND3 gene contains an additional exon of 57 bp, which is not present in the other two KCND genes and gives rise to the C-terminal splice KCND3L variant with an insertion of 19 amino acids. Copyright 2000 Academic Press.

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Year:  2000        PMID: 10729221     DOI: 10.1006/geno.2000.6117

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  27 in total

1.  Kinetic analysis of open- and closed-state inactivation transitions in human Kv4.2 A-type potassium channels.

Authors:  R Bähring; L M Boland; A Varghese; M Gebauer; O Pongs
Journal:  J Physiol       Date:  2001-08-15       Impact factor: 5.182

2.  Tuning pacemaker frequency of individual dopaminergic neurons by Kv4.3L and KChip3.1 transcription.

Authors:  B Liss; O Franz; S Sewing; R Bruns; H Neuhoff; J Roeper
Journal:  EMBO J       Date:  2001-10-15       Impact factor: 11.598

3.  UM 9(5)h and UM 9(5)p, human and porcine noncoding transcripts with preferential expression in the cerebellum.

Authors:  Uwe Michel; Boris Kallmann; Peter Rieckmann; Dirk Isbrandt
Journal:  RNA       Date:  2002-12       Impact factor: 4.942

4.  Molecular and functional characterization of Kv4.2 and KChIP2 expressed in the porcine left ventricle.

Authors:  Jobst-Hendrik Schultz; Tilmann Volk; Peter Bassalaý; J Christopher Hennings; Christian A Hübner; Heimo Ehmke
Journal:  Pflugers Arch       Date:  2007-01-23       Impact factor: 3.657

5.  Kv4.2 is a locus for PKC and ERK/MAPK cross-talk.

Authors:  Laura A Schrader; Yajun Ren; Feng Cheng; Dui Bui; J David Sweatt; Anne E Anderson
Journal:  Biochem J       Date:  2009-02-01       Impact factor: 3.857

6.  Circadian regulation of a-type potassium currents in the suprachiasmatic nucleus.

Authors:  Jason N Itri; Andrew M Vosko; Analyne Schroeder; Joanna M Dragich; Stephan Michel; Christopher S Colwell
Journal:  J Neurophysiol       Date:  2009-11-25       Impact factor: 2.714

7.  Modulation of human Kv4.3/KChIP2 channel inactivation kinetics by cytoplasmic Ca2.

Authors:  Christiane Groen; Robert Bähring
Journal:  Pflugers Arch       Date:  2017-07-22       Impact factor: 3.657

Review 8.  Transmural gradients in ion channel and auxiliary subunit expression.

Authors:  David McKinnon; Barbara Rosati
Journal:  Prog Biophys Mol Biol       Date:  2016-10-01       Impact factor: 3.667

9.  Modulation of Kv4.2 channel expression and gating by dipeptidyl peptidase 10 (DPP10).

Authors:  Henry H Jerng; Yan Qian; Paul J Pfaffinger
Journal:  Biophys J       Date:  2004-10       Impact factor: 4.033

10.  A VAMP7/Vti1a SNARE complex distinguishes a non-conventional traffic route to the cell surface used by KChIP1 and Kv4 potassium channels.

Authors:  Sarah E Flowerdew; Robert D Burgoyne
Journal:  Biochem J       Date:  2009-03-15       Impact factor: 3.857

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