Shyjan A W, Canfield V A, Levenson R
Department of Cell Biology, Yale University School of Medicine, New Haven, Connecticut 06510.
Genomics. 1991 Oct;11(2):435-42. doi: 10.1016/0888-7543(91)90152-5.
We have cloned and characterized the mouse Na,K-ATPase beta 2 subunit gene (Atp1b2). The gene spans approximately 7 kb and is split into seven exons. The transcription initiation site has been mapped and consensus TATA and putative CAAT sequences have been found at positions -23 and -137, respectively. Discrete structural domains of the beta 2 subunit protein are encoded by separate exons: The intracellular amino-terminal and putative transmembrane domains are encoded by individual exons and the extracellular carboxyl-terminal domain is encoded by five exons. The exon/intron organization of the beta 2 subunit gene closely resembles that of the H,K-ATPase beta subunit gene, suggesting that these two genes evolved from a common evolutionary ancestor. Comparison of the promoter region of the mouse and rat beta 2 subunit genes reveals a remarkably high degree of homology within a 788-nucleotide segment immediately upstream of the transcription start site. This observation suggests that elements that serve to regulate the cell-specific expression of the beta 2 subunit gene are likely to be located within this conserved region.
我们已经克隆并鉴定了小鼠钠钾ATP酶β2亚基基因(Atp1b2)。该基因跨度约7kb,分为7个外显子。已确定转录起始位点,并分别在-23和-137位置发现了共有TATA序列和推定的CAAT序列。β2亚基蛋白的离散结构域由单独的外显子编码:细胞内氨基末端和推定的跨膜结构域由单个外显子编码,细胞外羧基末端结构域由5个外显子编码。β2亚基基因的外显子/内含子组织与H,K-ATP酶β亚基基因非常相似,表明这两个基因起源于共同的进化祖先。对小鼠和大鼠β2亚基基因启动子区域的比较显示,在转录起始位点上游紧邻的788个核苷酸片段内具有非常高的同源性。这一观察结果表明,用于调节β2亚基基因细胞特异性表达的元件可能位于这个保守区域内。