Kim S Y, Ang S L, Bloch D B, Bloch K D, Kawahara Y, Tolman C, Lee R, Seidman J G, Neer E J
Department of Medicine, Brigham and Women's Hospital, Boston, MA 02115.
Proc Natl Acad Sci U S A. 1988 Jun;85(12):4153-7. doi: 10.1073/pnas.85.12.4153.
The guanine nucleotide-binding proteins (G proteins), which mediate hormonal regulation of many membrane functions, are composed of alpha, beta, and gamma subunits. We have cloned and characterized cDNA from a human T-cell library encoding a form of alpha i that is different from the human alpha i subtypes previously reported [Didsbury, J. R., Ho, Y.-S. & Snyderman, R. (1987) FEBS Lett. 211, 160-164 and Bray, P., Carter, A., Guo, V., Puckett, C., Kamholz, J., Spiegel, A. & Nirenberg, M. (1987) Proc. Natl. Acad. Sci. USA 84, 5115-5119]. alpha i is the alpha subunit of a class of G proteins that inhibits adenylate cyclase and regulates other enzymes and ion channels. This cDNA encodes a polypeptide of 354 amino acids and is assigned to encode the alpha i-3 subtype of G proteins on the basis of its similarity to other alpha i-like cDNAs and the presence of a predicted site for ADP ribosylation by pertussis toxin. We have determined the expression of mRNA for this and two other subtypes of human alpha i (alpha i-1 and alpha i-2) in a variety of human fetal tissues and in human cell lines. All three alpha i subtypes were present in the tissues tested. However, analysis of individual cell types reveals specificity of alpha i-1 expression. mRNA for alpha i-1 is absent in T cells, B cells, and monocytes but is present in other cell lines. The finding of differential expression of alpha i-1 genes may permit characterization of distinct physiological roles for this alpha i subunit. mRNA for alpha i-2 and alpha i-3 was found in all the primary and transformed cell lines tested. Thus, some cells contain all three alpha i subtypes. This observation raises the question of how cells prevent cross talk among receptors that are coupled to effectors through such similar alpha proteins.
鸟嘌呤核苷酸结合蛋白(G蛋白)介导许多膜功能的激素调节,由α、β和γ亚基组成。我们从人T细胞文库中克隆并鉴定了编码一种αi形式的cDNA,该αi与先前报道的人αi亚型不同[迪兹伯里,J.R.,何,Y.-S. & 斯奈德曼,R.(1987年)《欧洲生物化学学会联合会快报》211,160 - 164;布雷,P.,卡特,A.,郭,V.,帕克特,C.,坎霍尔兹,J.,斯皮格尔,A. & 尼伦伯格,M.(1987年)《美国国家科学院院刊》84,5115 - 5119]。αi是一类G蛋白的α亚基,可抑制腺苷酸环化酶并调节其他酶和离子通道。该cDNA编码一个354个氨基酸的多肽,基于其与其他αi样cDNA的相似性以及存在百日咳毒素ADP核糖基化的预测位点,被指定编码G蛋白的αi - 3亚型。我们已经确定了这种αi以及人αi的其他两种亚型(αi - 1和αi - 2)的mRNA在多种人胎儿组织和人细胞系中的表达情况。所有三种αi亚型都存在于所测试的组织中。然而,对单个细胞类型的分析揭示了αi - 1表达的特异性。αi - 1的mRNA在T细胞、B细胞和单核细胞中不存在,但在其他细胞系中存在。αi - 1基因差异表达的发现可能有助于确定该αi亚基不同的生理作用。在所有测试的原代和转化细胞系中都发现了αi - 2和αi - 3的mRNA。因此,一些细胞包含所有三种αi亚型。这一观察结果提出了一个问题,即细胞如何防止通过如此相似的α蛋白与效应器偶联的受体之间的相互干扰。