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钾依赖性钠钙交换器基因家族第三个成员NCKX3的分子克隆

Molecular cloning of a third member of the potassium-dependent sodium-calcium exchanger gene family, NCKX3.

作者信息

Kraev A, Quednau B D, Leach S, Li X F, Dong H, Winkfein R, Perizzolo M, Cai X, Yang R, Philipson K D, Lytton J

机构信息

C. H. Best Institute, Banting and Best Department of Medical Research, University of Toronto, Toronto, Ontario M5G 1L6, Canada.

出版信息

J Biol Chem. 2001 Jun 22;276(25):23161-72. doi: 10.1074/jbc.M102314200. Epub 2001 Apr 9.

DOI:10.1074/jbc.M102314200
PMID:11294880
Abstract

We describe here the identification and characterization of a novel member of the family of K(+)-dependent Na(+)/Ca(2+) exchangers, NCKX3 (gene SLC24A3). Human NCKX3 encodes a protein of 644 amino acids that displayed a high level of sequence identity to the other family members, rod NCKX1 and cone/neuronal NCKX2, in the hydrophobic regions surrounding the "alpha -repeat" sequences thought to form the ion-binding pocket for transport. Outside of these regions NCKX3 showed no significant identity to other known proteins. As anticipated from this sequence similarity, NCKX3 displayed K(+)-dependent Na(+)/Ca(2+) exchanger activity when assayed in heterologous expression systems, using digital imaging of fura-2 fluorescence, electrophysiology, or radioactive (45)Ca(2+) uptake. The N-terminal region of NCKX3, although not essential for expression, increased functional activity at least 10-fold and may represent a cleavable signal sequence. NCKX3 transcripts were most abundant in brain, with highest levels found in selected thalamic nuclei, in hippocampal CA1 neurons, and in layer IV of the cerebral cortex. Many other tissues also expressed NCKX3 at lower levels, especially aorta, uterus, and intestine, which are rich in smooth muscle. The discovery of NCKX3 thus expands the K(+)-dependent Na(+)/Ca(2+) exchanger family and suggests this class of transporter has a more widespread role in cellular Ca(2+) handling than previously appreciated.

摘要

我们在此描述了一种新型钾离子依赖型钠钙交换体NCKX3(基因SLC24A3)家族成员的鉴定与特性。人类NCKX3编码一种由644个氨基酸组成的蛋白质,该蛋白质在围绕被认为形成离子转运结合口袋的“α重复”序列的疏水区域,与该家族的其他成员——视杆细胞NCKX1和视锥细胞/神经元NCKX2,具有高度的序列同一性。在这些区域之外,NCKX3与其他已知蛋白质没有显著的同一性。基于这种序列相似性可以预期,当在异源表达系统中使用fura - 2荧光数字成像、电生理学或放射性(45)Ca(2+)摄取进行检测时,NCKX3表现出钾离子依赖型钠钙交换体活性。NCKX3的N端区域虽然对表达不是必需的,但至少使功能活性提高了10倍,可能代表一个可切割的信号序列。NCKX3转录本在脑中最为丰富,在选定的丘脑核团、海马CA1神经元和大脑皮层IV层中含量最高。许多其他组织也以较低水平表达NCKX3,尤其是富含平滑肌的主动脉、子宫和肠道。因此,NCKX3的发现扩展了钾离子依赖型钠钙交换体家族,并表明这类转运蛋白在细胞钙处理中的作用比之前认识到的更为广泛。

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