Literature DB >> 20558321

Gain-of-function mutation S422L in the KCNJ8-encoded cardiac K(ATP) channel Kir6.1 as a pathogenic substrate for J-wave syndromes.

Argelia Medeiros-Domingo1, Bi-Hua Tan, Lia Crotti, David J Tester, Lee Eckhardt, Alessandra Cuoretti, Stacie L Kroboth, Chunhua Song, Qing Zhou, Doug Kopp, Peter J Schwartz, Jonathan C Makielski, Michael J Ackerman.   

Abstract

BACKGROUND: J-wave syndromes have emerged conceptually to encompass the pleiotropic expression of J-point abnormalities including Brugada syndrome (BrS) and early repolarization syndrome (ERS). KCNJ8, which encodes the cardiac K(ATP) Kir6.1 channel, recently has been implicated in ERS following identification of the functionally uncharacterized missense mutation S422L.
OBJECTIVE: The purpose of this study was to further explore KCNJ8 as a novel susceptibility gene for J-wave syndromes.
METHODS: Using polymerase chain reaction, denaturing high-performance liquid chromatography, and direct DNA sequencing, comprehensive open reading frame/splice site mutational analysis of KCNJ8 was performed in 101 unrelated patients with J-wave syndromes, including 87 with BrS and 14 with ERS. Six hundred healthy individuals were examined to assess the allelic frequency for all variants detected. KCNJ8 mutation(s) was engineered by site-directed mutagenesis and coexpressed heterologously with SUR2A in COS-1 cells. Ion currents were recorded using whole-cell configuration of the patch-clamp technique.
RESULTS: One BrS case and one ERS case hosted the identical missense mutation S422L, which was reported previously. KCNJ8-S422L involves a highly conserved residue and was absent in 1,200 reference alleles. Both cases were negative for mutations in all known BrS and ERS susceptibility genes. K(ATP) current of the Kir6.1-S422L mutation was increased significantly over the voltage range from 0 to 40 mV compared to Kir6.1-WT channels (n = 16-21; P <.05).
CONCLUSION: These findings further implicate KCNJ8 as a novel J-wave syndrome susceptibility gene and a marked gain of function in the cardiac K(ATP) Kir6.1 channel secondary to KCNJ8-S422L as a novel pathogenic mechanism for the phenotypic expression of both BrS and ERS.
Copyright © 2010 Heart Rhythm Society. Published by Elsevier Inc. All rights reserved.

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Year:  2010        PMID: 20558321      PMCID: PMC3049900          DOI: 10.1016/j.hrthm.2010.06.016

Source DB:  PubMed          Journal:  Heart Rhythm        ISSN: 1547-5271            Impact factor:   6.343


  39 in total

1.  Molecular assembly and subcellular distribution of ATP-sensitive potassium channel proteins in rat hearts.

Authors:  Akihiko Kuniyasu; Kazuyoshi Kaneko; Kohichi Kawahara; Hitoshi Nakayama
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Review 2.  A view of sur/KIR6.X, KATP channels.

Authors:  A P Babenko; L Aguilar-Bryan; J Bryan
Journal:  Annu Rev Physiol       Date:  1998       Impact factor: 19.318

3.  Different responses of epicardium and endocardium to KATP channel modulators during regional ischemia.

Authors:  S Miyoshi; T Miyazaki; K Moritani; S Ogawa
Journal:  Am J Physiol       Date:  1996-07

4.  Molecular characterization of human SUR2-containing K(ATP) channels.

Authors:  R Davis-Taber; W Choi; J Feng; L Hoogenboom; T McNally; P Kroeger; C C Shieh; R Simmer; J D Brioni; J P Sullivan; M Gopalakrishnan; V E Scott
Journal:  Gene       Date:  2000-10-03       Impact factor: 3.688

5.  Mouse model of Prinzmetal angina by disruption of the inward rectifier Kir6.1.

Authors:  Takashi Miki; Masashi Suzuki; Tadao Shibasaki; Hiroko Uemura; Toshiaki Sato; Kaori Yamaguchi; Haruhiko Koseki; Toshihiko Iwanaga; Haruaki Nakaya; Susuma Seino
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6.  Genetic basis and molecular mechanism for idiopathic ventricular fibrillation.

Authors:  Q Chen; G E Kirsch; D Zhang; R Brugada; J Brugada; P Brugada; D Potenza; A Moya; M Borggrefe; G Breithardt; R Ortiz-Lopez; Z Wang; C Antzelevitch; R E O'Brien; E Schulze-Bahr; M T Keating; J A Towbin; Q Wang
Journal:  Nature       Date:  1998-03-19       Impact factor: 49.962

7.  Role of ATP-sensitive K+ channel on ECG ST segment elevation during a bout of myocardial ischemia. A study on epicardial mapping in dogs.

Authors:  I Kubota; M Yamaki; T Shibata; E Ikeno; Y Hosoya; H Tomoike
Journal:  Circulation       Date:  1993-10       Impact factor: 29.690

8.  Absence of Kir6.1/KCNJ8 mutations in Italian patients with abnormal coronary vasomotion.

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9.  Molecular heterogeneity of calcium channel beta-subunits in canine and human heart: evidence for differential subcellular localization.

Authors:  Jason D Foell; Ravi C Balijepalli; Brian P Delisle; Anne Marie R Yunker; Seth L Robia; Jeffrey W Walker; Maureen W McEnery; Craig T January; Timothy J Kamp
Journal:  Physiol Genomics       Date:  2004-04-13       Impact factor: 3.107

Review 10.  Gene targeting approach to clarification of ion channel function: studies of Kir6.x null mice.

Authors:  Susumu Seino; Takashi Miki
Journal:  J Physiol       Date:  2003-06-25       Impact factor: 5.182

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  108 in total

Review 1.  The electrocardiographic early repolarization pattern in athletes: normal variant or sudden death risk factor?

Authors:  Varsha Keelara Tanguturi; Peter A Noseworthy; Christopher Newton-Cheh; Aaron L Baggish
Journal:  Sports Med       Date:  2012-05-01       Impact factor: 11.136

2.  Loss-of-function mutations in the KCNJ8-encoded Kir6.1 K(ATP) channel and sudden infant death syndrome.

Authors:  David J Tester; Bi-Hua Tan; Argelia Medeiros-Domingo; Chunhua Song; Jonathan C Makielski; Michael J Ackerman
Journal:  Circ Cardiovasc Genet       Date:  2011-08-11

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Authors:  Hiroshi Watanabe; Tohru Minamino
Journal:  J Hum Genet       Date:  2015-07-30       Impact factor: 3.172

Review 4.  KATP Channels in the Cardiovascular System.

Authors:  Monique N Foster; William A Coetzee
Journal:  Physiol Rev       Date:  2016-01       Impact factor: 37.312

Review 5.  Early repolarization syndrome: A cause of sudden cardiac death.

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Journal:  World J Cardiol       Date:  2015-08-26

Review 6.  Genetic testing for inherited cardiac disease.

Authors:  Arthur A M Wilde; Elijah R Behr
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Review 7.  Phenotypical manifestations of mutations in the genes encoding subunits of the cardiac voltage-dependent L-type calcium channel.

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Journal:  Circ Res       Date:  2011-03-04       Impact factor: 17.367

8.  ABCC9 is a novel Brugada and early repolarization syndrome susceptibility gene.

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9.  Spectrum and prevalence of mutations involving BrS1- through BrS12-susceptibility genes in a cohort of unrelated patients referred for Brugada syndrome genetic testing: implications for genetic testing.

Authors:  Lia Crotti; Cherisse A Marcou; David J Tester; Silvia Castelletti; John R Giudicessi; Margherita Torchio; Argelia Medeiros-Domingo; Savastano Simone; Melissa L Will; Federica Dagradi; Peter J Schwartz; Michael J Ackerman
Journal:  J Am Coll Cardiol       Date:  2012-07-25       Impact factor: 24.094

Review 10.  KATP channels and cardiovascular disease: suddenly a syndrome.

Authors:  Colin G Nichols; Gautam K Singh; Dorothy K Grange
Journal:  Circ Res       Date:  2013-03-29       Impact factor: 17.367

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