Hasebe M, Hanada H, Moriyama Y, Maeda M, Futai M
Department of Organic Chemistry and Biochemistry, Osaka University, Japan.
Biochem Biophys Res Commun. 1992 Mar 16;183(2):856-63. doi: 10.1016/0006-291x(92)90562-y.
Genes for the human vacuolar type H(+)-ATPase proteolipid (16-kDa) subunit were cloned and their nucleotide sequences were determined. Comparison of the deduced sequences indicated that at least four genes including pseudogenes are present in the human genome. One of them corresponded to that for the 16-kDa subunit expressed in HeLa cells. The coding sequence was separated by two introns. The second intron was located in the DNA segment giving a loop between the second and third transmembrane helices, supporting the idea that the 16-kDa subunit was evolved by gene duplication. The primary sequence determined from the second clone had a termination codon behind the third transmembrane helix. Possible translation products from the other two clones had no putative acidic residues essential for proton transport function of the 16-kDa subunit. Thus, it is interesting to know whether these genes are transcribed, since they may have unique cellular functions.
克隆了人类液泡型H(+)-ATP酶蛋白脂质(16 kDa)亚基的基因,并测定了其核苷酸序列。对推导序列的比较表明,人类基因组中至少存在包括假基因在内的四个基因。其中一个与在HeLa细胞中表达的16 kDa亚基的基因相对应。编码序列被两个内含子隔开。第二个内含子位于在第二和第三跨膜螺旋之间形成环的DNA片段中,这支持了16 kDa亚基是通过基因复制进化而来的观点。从第二个克隆中确定的一级序列在第三个跨膜螺旋后面有一个终止密码子。来自其他两个克隆的可能翻译产物没有16 kDa亚基质子转运功能所必需的假定酸性残基。因此,了解这些基因是否被转录很有意思,因为它们可能具有独特的细胞功能。