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Science 17 November 1995: Vol. 270. no. 5239, pp. 1166 - 1170 DOI: 10.1126/science.270.5239.1166
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Research Articles
Reconstitution of I : An Inward
Rectifier Subunit Plus the Sulfonylurea Receptor
Nobuya Inagaki (1),
Tohru Gonoi (1),
John P. Clement IV,
Noriyuki Namba,
Johji Inazawa,
Gabriela Gonzalez,
Lydia Aguilar-Bryan,
Susumu Seino (2),
Joseph Bryan
A member of the inwardly rectifying potassium channel family was
cloned here. The channel, called BIR (Kir6.2), was expressed in large
amounts in rat pancreatic islets and glucose-responsive
insulin-secreting cell lines. Coexpression with the sulfonylurea
receptor SUR reconstituted an inwardly rectifying potassium conductance
of 76 picosiemens that was sensitive to adenosine triphosphate (ATP)
(I ) and was inhibited by sulfonylureas and
activated by diazoxide. The data indicate that these pancreatic
cell potassium channels are a complex composed of at least two
subunits-BIR, a member of the inward rectifier potassium channel
family, and SUR, a member of the ATP-binding cassette superfamily. Gene
mapping data show that these two potassium channel subunit genes are
clustered on human chromosome 11 at position 11p15.1.
N. Inagaki, N. Namba, and S. Seino are in the Division of
Molecular Medicine, Center for Biomedical Science, Chiba University
School of Medicine, Chuo-ku, Chiba 260, Japan. T. Gonoi is in the
Research Center for Pathogenic Fungi and Microbial Toxicoses, Chiba
University, Chuo-ku, Chiba 260, Japan. J. P. Clement IV, G. Gonzalez,
L. Aguilar-Bryan, and J. Bryan are in the Departments of Cell Biology
and Medicine, Baylor College of Medicine, Houston, TX 77030, USA. J.
Inazawa is in the Department of Hygiene, Kyoto Prefectural University
of Medicine, Kamigyo-ku, Kyoto 602, Japan.
(1) These authors contributed equally to this study.
(2) To whom correspondence should be addressed.
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282, 9628-9634
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- An ATP-Binding Mutation (G334D) in KCNJ11 Is Associated With a Sulfonylurea-Insensitive Form of Developmental Delay, Epilepsy, and Neonatal Diabetes.
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282, 1747-1756
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9, 30-36
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- Protection conferred by myocardial ATP-sensitive K+ channels in pressure overload-induced congestive heart failure revealed in KCNJ11 Kir6.2-null mutant.
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577, 1053-1065
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J. Physiol.
577, 17-29
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355, 456-466
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N. Engl. J. Med.
355, 507-510
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573, 595-609
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571, 3-14
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- P. E MacDonald, J. W Joseph, and P. Rorsman (2005)
Phil Trans R Soc B
360, 2211-2225
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289, C1351-C1359
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- C. Shiota, J. V. Rocheleau, M. Shiota, D. W. Piston, and M. A. Magnuson (2005)
Am J Physiol Endocrinol Metab
289, E570-E577
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Hum. Mol. Genet.
14, 2717-2726
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- Severe Congenital Hyperinsulinism Caused by a Mutation in the Kir6.2 Subunit of the Adenosine Triphosphate-Sensitive Potassium Channel Impairing Trafficking and Function.
- E. Marthinet, A. Bloc, Y. Oka, Y. Tanizawa, B. Wehrle-Haller, V. Bancila, J.-M. Dubuis, J. Philippe, and V. M. Schwitzgebel (2005)
J. Clin. Endocrinol. Metab.
90, 5401-5406
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Diabetes
54, 2503-2513
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J. Gen. Physiol.
126, 285-299
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Physiol Genomics
22, 204-212
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J. Physiol.
565, 731-741
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- C. Ezenwaka, R. Kalloo, M. Uhlig, R. Schwenk, and J. Eckel (2005)
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185, 439-444
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- The C42R Mutation in the Kir6.2 (KCNJ11) Gene as a Cause of Transient Neonatal Diabetes, Childhood Diabetes, or Later-Onset, Apparently Type 2 Diabetes Mellitus.
- T. Yorifuji, K. Nagashima, K. Kurokawa, M. Kawai, M. Oishi, Y. Akazawa, M. Hosokawa, Y. Yamada, N. Inagaki, and T. Nakahata (2005)
J. Clin. Endocrinol. Metab.
90, 3174-3178
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- Susceptibility of the heart to ischaemia-reperfusion injury and exercise-induced cardioprotection are sex-dependent in the rat.
- D. A Brown, J. M Lynch, C. J Armstrong, N. M Caruso, L. B Ehlers, M. S Johnson, and R. L Moore (2005)
J. Physiol.
564, 619-630
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- The Size of a Single Residue of the Sulfonylurea Receptor Dictates the Effectiveness of KATP Channel Openers.
- C. Moreau, F. Gally, H. Jacquet-Bouix, and M. Vivaudou (2005)
Mol. Pharmacol.
67, 1026-1033
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- MARCH-II Is a Syntaxin-6-binding Protein Involved in Endosomal Trafficking.
- N. Nakamura, H. Fukuda, A. Kato, and S. Hirose (2005)
Mol. Biol. Cell
16, 1696-1710
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- Two SUR1-specific Histidine Residues Mandatory for Zinc-induced Activation of the Rat KATP Channel.
- V. Bancila, T. Cens, D. Monnier, F. Chanson, C. Faure, Y. Dunant, and A. Bloc (2005)
J. Biol. Chem.
280, 8793-8799
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- Regulation of ATP-sensitive Potassium Channel Subunit Kir6.2 Expression in Rat Intestinal Insulin-producing Progenitor Cells.
- T. Hashimoto, T. Nakamura, H. Maegawa, Y. Nishio, K. Egawa, and A. Kashiwagi (2005)
J. Biol. Chem.
280, 1893-1900
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- Molecular Diversity and Regulation of Renal Potassium Channels.
- S. C. Hebert, G. Desir, G. Giebisch, and W. Wang (2005)
Physiol Rev
85, 319-371
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- H3 Domain of Syntaxin 1A Inhibits KATP Channels by Its Actions on the Sulfonylurea Receptor 1 Nucleotide-Binding Folds-1 and -2.
- N. Cui, Y. Kang, Y. He, Y.-M. Leung, H. Xie, E. A. Pasyk, X. Gao, L. Sheu, J. B. Hansen, P. Wahl, et al. (2004)
J. Biol. Chem.
279, 53259-53265
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- Molecular basis of Kir6.2 mutations associated with neonatal diabetes or neonatal diabetes plus neurological features.
- P. Proks, J. F. Antcliff, J. Lippiat, A. L. Gloyn, A. T. Hattersley, and F. M. Ashcroft (2004)
PNAS
101, 17539-17544
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- Polymorphisms of the SUR1 (ABCC8) and Kir6.2 (KCNJ11) Genes Predict the Conversion from Impaired Glucose Tolerance to Type 2 Diabetes. The Finnish Diabetes Prevention Study.
- O. Laukkanen, J. Pihlajamaki, J. Lindstrom, J. Eriksson, T. T. Valle, H. Hamalainen, P. Ilanne-Parikka, S. Keinanen-Kiukaanniemi, J. Tuomilehto, M. Uusitupa, et al. (2004)
J. Clin. Endocrinol. Metab.
89, 6286-6290
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- Impact of Treatment on Islet Function in Type 2 Diabetes.
- J.-C. Henquin, C. Boitard, E. Cerasi, E. Ferrannini, D. F. Steiner, and S. Efendic (2004)
Diabetes
53, S1-S5
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- Metabolic Regulation of the Pancreatic Beta-Cell ATP-Sensitive K+ Channel: A Pas de Deux.
- A. Tarasov, J. Dusonchet, and F. Ashcroft (2004)
Diabetes
53, S113-S122
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- ATP-Sensitive K+ Channel Knockout Compromises the Metabolic Benefit of Exercise Training, Resulting in Cardiac Deficits.
- G. C. Kane, A. Behfar, S. Yamada, C. Perez-Terzic, F. O'Cochlain, S. Reyes, P. P. Dzeja, T. Miki, S. Seino, and A. Terzic (2004)
Diabetes
53, S169-S175
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- Roles of ATP-Sensitive K+ Channels as Metabolic Sensors: Studies of Kir6.x Null Mice.
- K. Minami, T. Miki, T. Kadowaki, and S. Seino (2004)
Diabetes
53, S176-S180
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- Syntaxin-1A Inhibits Cardiac KATP Channels by Its Actions on Nucleotide Binding Folds 1 and 2 of Sulfonylurea Receptor 2A.
- Y. Kang, Y.-M. Leung, J. E. Manning-Fox, F. Xia, H. Xie, L. Sheu, R. G. Tsushima, P. E. Light, and H. Y. Gaisano (2004)
J. Biol. Chem.
279, 47125-47131
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- Mutation in Nucleotide-Binding Domains of Sulfonylurea Receptor 2 Evokes Na-ATP-Dependent Activation of ATP-Sensitive K+ Channels: Implication for Dimerization of Nucleotide-Binding Domains to Induce Channel Opening.
- M. Yamada, M. Ishii, H. Hibino, and Y. Kurachi (2004)
Mol. Pharmacol.
66, 807-816
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- Natriuretic Peptide Receptor-C Regulates Coronary Blood Flow and Prevents Myocardial Ischemia/Reperfusion Injury: Novel Cardioprotective Role for Endothelium-Derived C-Type Natriuretic Peptide.
- A. Hobbs, P. Foster, C. Prescott, R. Scotland, and A. Ahluwalia (2004)
Circulation
110, 1231-1235
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- Disruption of Glucose Sensing and Insulin Secretion by Ribozyme Kir6.2-Gene Targeting in Insulin-Secreting Cells.
- L. Li, A. Rojas, J. Wu, and C. Jiang (2004)
Endocrinology
145, 4408-4414
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- Fenofibrate, Troglitazone, and 15-Deoxy-{Delta}12,14-prostaglandin J2 Close KATP Channels and Induce Insulin Secretion.
- K. Shimomura, H. Shimizu, M. Ikeda, S. Okada, M. Kakei, S. Matsumoto, and M. Mori (2004)
J. Pharmacol. Exp. Ther.
310, 1273-1280
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