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Cloning and sequencing of a processed pseudogene derived from a human class III alcohol dehydrogenase gene.

机译:源自人类III类醇脱氢酶基因的加工假基因的克隆和测序。

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摘要

Current information on the molecular structure of human alcohol dehydrogenase (ADH) genes is fragmentary. To characterize all ADH genes, we have isolated 63 ADH clones from human genomic libraries made from one individual. Fifty-nine clones have been classified into five previously known loci: ADH1 (18 clones), ADH2 (20 clones), and ADH3 class I (16 clones), ADH4 class II (4 clones), and ADH5 class III (1 clone). Sequencing of one of the remaining four unclassified clones, SY lambda ADHE38, about 1.1 kb in length, shows no introns and three frameshift mutations in the coding region, with a total of 10 internal termination codons. When its deduced amino acid sequence was compared with those of the class I, class II, and class III ADHs, the proportions of identical amino acids were 56.7%, 55.5%, and 88.7%, respectively, suggesting that the processed pseudogene was derived from an ADH5 gene. The duplication event seems to have occurred about 3.5 million years ago, and the pseudogene has undergone a rapid change since then.
机译:有关人类酒精脱氢酶(ADH)基因的分子结构的当前信息尚不完整。为了表征所有ADH基因,我们从一个人的基因组文库中分离出63个ADH克隆。 59个克隆已分类为五个先前已知的基因座:ADH1(18个克隆),ADH2(20个克隆)和IDH3 I类(16个克隆),ADH4 II类(4个克隆)和ADH5 III类(1个克隆) 。其余四个未分类克隆之一的SYλADHE38的序列长约1.1 kb,显示在编码区中没有内含子和三个移码突变,共有10个内部终止密码子。当将其推导的氨基酸序列与I,II和III类ADH的氨基酸序列进行比较时,相同氨基酸的比例分别为56.7%,55.5%和88.7%,这表明加工的假基因来源于ADH5基因。复制事件似乎发生在大约350万年前,从那时起,伪基因发生了迅速的变化。

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