Literature DB >> 1381835

Cloning of ShIII (Shaw-like) cDNAs encoding a novel high-voltage-activating, TEA-sensitive, type-A K+ channel.

E Vega-Saenz de Miera1, H Moreno, D Fruhling, C Kentros, B Rudy.   

Abstract

Transient voltage-dependent potassium (K+) currents, also known as A currents, have been of great interest to neurophysiologists due to their special roles in neuronal excitability. Several cDNAs encoding transcripts expressing A currents have been characterized. Recently, a cDNA (KShIIIC or Raw3) was isolated which expresses an unusual A current that is highly sensitive to TEA, and activates at potentials more positive than -20 mV. Channels containing this protein may have specialized roles in modulating the electrical behaviour of neurons. Here we report the isolation and characterization of two rat cDNAs corresponding to two alternatively spliced transcripts (KShIIID.1 and KShIIID.2) from another gene (KShIIID) of the same subfamily as KShIIIC, the ShIII or Shaw-related gene subfamily. KShIIID.1 also expresses an unusual high-voltage-activating, TEA-sensitive A-type channel. There are, however, significant differences between KShIIIC and KShIIID channels which may have interesting functional consequences. The two most important differences are: (i) KShIIID channels conduct in the steady-state over a much broader window of potentials than KShIIIC; this reflects differences between the kinetic schemes of the two channels; and (ii) KShIIID inactivates with significantly slower kinetics than KShIIIC. The identification of KShIIID transcripts contributes to our knowledge of the molecular components that may determine the functional diversity of A currents and provides exciting opportunities to increase our understanding of the structure and function of K+ channels.

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Year:  1992        PMID: 1381835     DOI: 10.1098/rspb.1992.0036

Source DB:  PubMed          Journal:  Proc Biol Sci        ISSN: 0962-8452            Impact factor:   5.349


  26 in total

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2.  Transient potassium currents regulate the discharge patterns of dorsal cochlear nucleus pyramidal cells.

Authors:  P O Kanold; P B Manis
Journal:  J Neurosci       Date:  1999-03-15       Impact factor: 6.167

3.  Molecular determinants of emerging excitability in rat embryonic motoneurons.

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4.  Casein kinase 2 determines the voltage dependence of the Kv3.1 channel in auditory neurons and transfected cells.

Authors:  C M Macica; L K Kaczmarek
Journal:  J Neurosci       Date:  2001-02-15       Impact factor: 6.167

Review 5.  Transient outward potassium current, 'Ito', phenotypes in the mammalian left ventricle: underlying molecular, cellular and biophysical mechanisms.

Authors:  Sangita P Patel; Donald L Campbell
Journal:  J Physiol       Date:  2005-04-14       Impact factor: 5.182

6.  Potassium currents of olfactory bulb juxtaglomerular cells: characterization, simulation, and implications for plateau potential firing.

Authors:  A V Masurkar; W R Chen
Journal:  Neuroscience       Date:  2011-06-13       Impact factor: 3.590

7.  T2N as a new tool for robust electrophysiological modeling demonstrated for mature and adult-born dentate granule cells.

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Journal:  Elife       Date:  2017-11-22       Impact factor: 8.140

8.  Regulation of Nociceptive Glutamatergic Signaling by Presynaptic Kv3.4 Channels in the Rat Spinal Dorsal Horn.

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9.  Regulation of ENaC-mediated sodium transport by glucocorticoids in Reissner's membrane epithelium.

Authors:  Sung Huhn Kim; Kyunghee X Kim; Nithya N Raveendran; Tao Wu; Satyanarayana R Pondugula; Daniel C Marcus
Journal:  Am J Physiol Cell Physiol       Date:  2009-01-14       Impact factor: 4.249

10.  Ternary Kv4.2 channels recapitulate voltage-dependent inactivation kinetics of A-type K+ channels in cerebellar granule neurons.

Authors:  Yimy Amarillo; Jose A De Santiago-Castillo; Kevin Dougherty; Jonathon Maffie; Elaine Kwon; Manuel Covarrubias; Bernardo Rudy
Journal:  J Physiol       Date:  2008-02-14       Impact factor: 5.182

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