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人载脂蛋白E cDNA克隆的鉴定及DNA序列分析

Identification and DNA sequence of a human apolipoprotein E cDNA clone.

作者信息

Breslow J L, McPherson J, Nussbaum A L, Williams H W, Lofquist-Kahl F, Karathanasis S K, Zannis V I

出版信息

J Biol Chem. 1982 Dec 25;257(24):14639-41.

PMID:6897404
Abstract

cDNA clones encoding human apolipoprotein E were identified by screening an adult human liver cDNA library with an oligonucleotide probe. The probe was a mixture of synthetic 14-base long DNA oligomers constructed to correspond to all possible codons for apo-E amino acids 218-222. Plasmids from four of the 20 clones selected by this screening procedure were digested with PstI and all had five internal PstI sites with a total length of the cDNA insert of approximately 900 base pairs. DNA sequence analysis of one of these clones, designated pE-301, revealed that it corresponded to apo-E amino acids 81-299, and contained a standard termination codon, polyadenylation signal, and poly A tail. The DNA sequence examined included the known apo-E polymorphic sites at amino acids 112, 145, and 158, and the mutant apo-E phenotypes can all be explained on the basis of a single base substitution in the first position of each of these codons. This work supports the hypothesis that the apo-E polymorphism is due to mutations in the region of DNA coding for the apo-E structural gene.

摘要

通过用寡核苷酸探针筛选成人肝脏cDNA文库,鉴定出编码人载脂蛋白E的cDNA克隆。该探针是由合成的14个碱基长的DNA寡聚物组成的混合物,构建该混合物以对应载脂蛋白E氨基酸218 - 222的所有可能密码子。通过该筛选程序从20个克隆中选出的4个克隆的质粒用PstI进行消化,所有质粒都有5个内部PstI位点,cDNA插入片段的总长度约为900个碱基对。对其中一个命名为pE - 301的克隆进行DNA序列分析,结果显示它对应于载脂蛋白E氨基酸81 - 299,并包含一个标准的终止密码子、聚腺苷酸化信号和聚A尾。所检测的DNA序列包括已知的载脂蛋白E在氨基酸112、145和158处的多态性位点,并且所有突变型载脂蛋白E表型都可以基于这些密码子第一个位置的单个碱基替换来解释。这项工作支持了载脂蛋白E多态性是由于载脂蛋白E结构基因编码区DNA突变所致的假说。

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