Literature DB >> 8647284

Kir2.2v: a possible negative regulator of the inwardly rectifying K+ channel Kir2.2.

N Namba1, N Inagaki, T Gonoi, Y Seino, S Seino.   

Abstract

We have cloned the human genes encoding the inwardly rectifying K+ (Kir) channel subunits, Kir2.2 (hKir2.2) and its variant, termed hKir2.2v. When expressed in Xenopus oocytes, hKir2.2 produced strong inwardly rectifying K+ currents, whereas the expression of hKir2.2v did not elicit significant currents. Coexpression of hKir2.2v with hKir2.2 showed an hKir2.2v inhibition of hKir2.2 K+ currents, indicating that it acts as a negative regulator of hKir2.2 channel activity. Mutational analysis of hKir2.2v and studies of chimeras between hKir2.2 and hKir2.2v suggest that the intracellular C-terminal region of hKir2.2v participates in the negative regulation of the hKir2.2v channel activity.

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Year:  1996        PMID: 8647284     DOI: 10.1016/0014-5793(96)00445-0

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  4 in total

1.  Kir2.6 regulates the surface expression of Kir2.x inward rectifier potassium channels.

Authors:  Lior Dassau; Lisa R Conti; Carolyn M Radeke; Louis J Ptáček; Carol A Vandenberg
Journal:  J Biol Chem       Date:  2011-01-05       Impact factor: 5.157

2.  Whole genome and exome sequencing realignment supports the assignment of KCNJ12, KCNJ17, and KCNJ18 paralogous genes in thyrotoxic periodic paralysis locus: functional characterization of two polymorphic Kir2.6 isoforms.

Authors:  Rolf M Paninka; Diego R Mazzotti; Marina M L Kizys; Angela C Vidi; Hélio Rodrigues; Silas P Silva; Ilda S Kunii; Gilberto K Furuzawa; Manoel Arcisio-Miranda; Magnus R Dias-da-Silva
Journal:  Mol Genet Genomics       Date:  2016-03-23       Impact factor: 3.291

3.  Human myoblast fusion requires expression of functional inward rectifier Kir2.1 channels.

Authors:  J Fischer-Lougheed; J H Liu; E Espinos; D Mordasini; C R Bader; D Belin; L Bernheim
Journal:  J Cell Biol       Date:  2001-05-14       Impact factor: 10.539

4.  Mutations in potassium channel Kir2.6 cause susceptibility to thyrotoxic hypokalemic periodic paralysis.

Authors:  Devon P Ryan; Magnus R Dias da Silva; Tuck Wah Soong; Bertrand Fontaine; Matt R Donaldson; Annie W C Kung; Wallaya Jongjaroenprasert; Mui Cheng Liang; Daphne H C Khoo; Jin Seng Cheah; Su Chin Ho; Harold S Bernstein; Rui M B Maciel; Robert H Brown; Louis J Ptácek
Journal:  Cell       Date:  2010-01-08       Impact factor: 41.582

  4 in total

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