Underhill D A, Canfield V A, Dahl J P, Gros P, Levenson R
Department of Biochemistry, McGill University, Montreal, Quebec, Canada H3G 1Y6.
Biochemistry. 1999 Nov 9;38(45):14746-51. doi: 10.1021/bi9916168.
We have isolated and characterized cDNA clones encoding the murine homologue of a putative fourth Na,K-ATPase alpha subunit isoform (alpha4). The predicted polypeptide is 1032 amino acids in length and exhibits 75% amino acid sequence identity to the rat alpha1, alpha2, and alpha3 subunits. Within the first extracellular loop, the alpha4 subunit is highly divergent from other Na,K-ATPase alpha subunits. Because this region of Na,K-ATPase is a major determinant of ouabain sensitivity, we tested the ability of the rodent alpha4 subunit to transfer ouabain resistance in a transfection protocol. We find that a cDNA containing the complete rodent alpha4 ORF is capable of conferring low levels of ouabain resistance upon HEK 293 cells, an indication that the alpha4 subunit can substitute for the endogenous ouabain-sensitive alpha subunit of human cells. Nucleotide sequences specific for the murine alpha4 subunit were used to identify the chromosomal position of the alpha4 subunit gene. By hybridizing an alpha4 probe with a series of BACs, we localized the alpha4 subunit gene (Atp1a4) to the distal portion of mouse chromosome 1, in very close proximity to the murine Na,K-ATPase alpha2 subunit gene. In adult mouse tissues, we detected expression of the alpha4 subunit gene almost exclusively in testis, with low levels of expression in epididymis. The close similarities in the organization and expression pattern of the murine and human alpha4 subunit genes suggest that these two genes are orthologous. Together, our studies indicate that the alpha4 subunit represents a functional Na,K-ATPase alpha subunit isoform.
我们已经分离并鉴定了编码假定的第四个钠钾-ATP酶α亚基异构体(α4)小鼠同源物的cDNA克隆。预测的多肽长度为1032个氨基酸,与大鼠α1、α2和α3亚基的氨基酸序列同一性为75%。在第一个细胞外环内,α4亚基与其他钠钾-ATP酶α亚基高度不同。由于钠钾-ATP酶的这一区域是哇巴因敏感性的主要决定因素,我们在转染实验中测试了啮齿动物α4亚基传递哇巴因抗性的能力。我们发现,包含完整啮齿动物α4开放阅读框的cDNA能够赋予HEK 293细胞低水平的哇巴因抗性,这表明α4亚基可以替代人类细胞内源性的哇巴因敏感α亚基。用于小鼠α4亚基的核苷酸序列被用来鉴定α4亚基基因的染色体位置。通过将α4探针与一系列细菌人工染色体(BAC)杂交,我们将α4亚基基因(Atp1a4)定位到小鼠染色体1的远端,非常靠近小鼠钠钾-ATP酶α2亚基基因。在成年小鼠组织中,我们几乎只在睾丸中检测到α4亚基基因的表达,在附睾中的表达水平较低。小鼠和人类α4亚基基因在组织和表达模式上的密切相似性表明这两个基因是直系同源的。总之,我们的研究表明α4亚基代表一种功能性的钠钾-ATP酶α亚基异构体。