CLONING AND FUNCTIONAL EXPRESSION OF THE CDNA-ENCODING AN INWARDLY-RECTIFYING POTASSIUM CHANNEL EXPRESSED IN PANCREATIC BETA-CELLS AND IN THE BRAIN

被引:47
作者
BOND, CT
AMMALA, C
ASHFIELD, R
BLAIR, TA
GRIBBLE, F
KHAN, RN
LEE, K
PROKS, P
ROWE, ICM
SAKURA, H
ASHFORD, MJ
ADELMAN, JP
ASHCROFT, FM
机构
[1] OREGON HLTH SCI UNIV,VOLLUM INST,PORTLAND,OR 97201
[2] UNIV OXFORD,PHYSIOL LAB,OXFORD OX1 3PT,ENGLAND
[3] UNIV CAMBRIDGE,DEPT PHARMACOL,CAMBRIDGE CB2 1QJ,ENGLAND
基金
英国惠康基金;
关键词
K-CHANNEL; INWARD RECTIFIER; ATP-SENSITIVE K-CHANNEL; PANCREATIC BETA-CELL; BIR1;
D O I
10.1016/0014-5793(95)00497-W
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A cDNA clone encoding an inwardly-rectifying K-channel (BIR1) was isolated from insulinoma cells. The predicted amino acid sequence shares 72% identity with the cardiac ATP-sensitive K-channel rcK(ATP)(K-ATP-1; [6]). The mRNA is expressed in the brain and insulinoma cells. Heterologous expression in Xenopus oocytes produced currents which were K+-selective, time-independent and showed inward rectification. The currents were blocked by external barium and caesium, but insensitive to tolbutamide and diazoxide. In inside-out patches, channel activity was not blocked by 1 mM internal ATP. The sequence homology with K-ATP-1 suggests that BIR1 is a subunit of a brain and beta-cell K-ATP channel. However, pharmacological differences and the lack of ATP-sensitivity, suggest that if, this is the case, heterologous subunits must exert strong modulatory influences on the native channel.
引用
收藏
页码:61 / 66
页数:6
相关论文
共 20 条
  • [1] Adelman, Shen, Kavanaugh, Warren, Wu, Lagrutta, Bond, North, Neuron, 9, pp. 209-216, (1992)
  • [2] Ashcroft, Ashcroft, Harrison, J. Physiol., 400, pp. 501-527, (1988)
  • [3] Ashcroft, Ashcroft, Insulin-Molecular Biology to Pathology, pp. 97-151, (1992)
  • [4] Ashcroft, Ashcroft, Biochim. Biophys. Acta, 1175, pp. 45-59, (1992)
  • [5] Ashcroft, Rorsman, Progr. Biophys. Molec. Biol., 54, pp. 87-143, (1989)
  • [6] Ashford, Bond, Blair, Adelman, Nature, 370, pp. 456-459
  • [7] Bond, Pessia, Xia, Lagrutta, Kavanaugh, Adelman, Receptor and Channels, 2, pp. 183-191, (1994)
  • [8] Ficker, Taglialatela, Wibble, Henley, Brown, Science, 266, pp. 1068-1072, (1994)
  • [9] Frohman, Dush, Martin, Proc. Natl. Acad. Sci. USA, 85, pp. 8998-9002, (1988)
  • [10] Heginbotham, Abramson, MacKinnon, Science, 258, pp. 1152-1155, (1992)