Takeyasu K, Tamkun M M, Siegel N R, Fambrough D M
J Biol Chem. 1987 Aug 5;262(22):10733-40.
A cDNA encoding the beta-subunit of the (Na+ + K+)-ATPase was cloned from a chicken brain cDNA library, and its nucleotide sequence was determined. High cross-species sequence homologies were found both in coding and noncoding regions. The cDNA was subcloned into a shuttle vector derived from pSV2CAT and was stably incorporated into mouse Ltk-cells. The avian beta-subunit was expressed on the cell surface (1-8 X 10(5) molecules/cell) complexed with alpha-subunits of the murine (Na+ + K+)-ATPase. In the hybrid system there was rapid assembly of subunits, post-translational N-glycosylations of the beta-subunit at its three Asn-X-Ser (or Thr) positions, and modification of high mannose oligosaccharides to complex type. Avian beta-subunits expressed in the mouse cells had an apparent molecular weight of about 55,000 as compared with 47,000 in avian cells, due to post-translational modifications, presumably differences in complex oligosaccharides. Despite the high number of interspecies hybrid (Na+ + K+)-ATPase molecules, the cells had none of the high affinity ouabain binding sites (KD = 2 X 10(-7) M) characteristic of avian cells, consistent with the view that the ouabain binding site is located largely or exclusively on the alpha-subunit and is not greatly affected by alpha-beta interaction.
从鸡脑cDNA文库中克隆出编码(Na⁺+K⁺)-ATP酶β亚基的cDNA,并测定了其核苷酸序列。在编码区和非编码区均发现了高度的跨物种序列同源性。将该cDNA亚克隆到源自pSV2CAT的穿梭载体中,并稳定整合到小鼠Ltk⁻细胞中。禽β亚基与鼠(Na⁺+K⁺)-ATP酶的α亚基复合后在细胞表面表达(1 - 8×10⁵个分子/细胞)。在杂交系统中,亚基迅速组装,β亚基在其三个Asn-X-Ser(或Thr)位置进行翻译后N-糖基化,并且高甘露糖寡糖被修饰为复合型。与禽细胞中47,000的表观分子量相比,在小鼠细胞中表达的禽β亚基的表观分子量约为55,000,这是由于翻译后修饰,推测是复合寡糖的差异所致。尽管存在大量种间杂交的(Na⁺+K⁺)-ATP酶分子,但这些细胞没有禽细胞特有的高亲和力哇巴因结合位点(KD = 2×10⁻⁷M),这与哇巴因结合位点主要或仅位于α亚基上且不受α-β相互作用很大影响的观点一致。