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人类多药耐药(mdr1)基因。cDNA克隆与转录起始

The human multidrug resistance (mdr1) gene. cDNA cloning and transcription initiation.

作者信息

Ueda K, Clark D P, Chen C J, Roninson I B, Gottesman M M, Pastan I

出版信息

J Biol Chem. 1987 Jan 15;262(2):505-8.

PMID:3027054
Abstract

Multidrug resistance in human KB carcinoma cells selected for resistance to colchicine, vinblastine, or adriamycin results from overexpression, and frequently amplification, of a specific gene (mdr1). Overlapping cDNA clones representing a complete 4.7-kilobase mdr1 transcript have been obtained from multidrug-resistant KB cells. Primer extension and S1 nuclease protection experiments show that two transcripts initiate 136 and 140 bases upstream from the first ATG codon in all human multidrug-resistant cell lines. The mdr1 gene is expressed in human normal kidney cells and HepG2 liver cells as a poly(A)+ RNA which starts from the same sites. Less prominent transcripts were found to initiate 155-180 bases upstream from the first ATG codon in vinblastine- or adriamycin-selected cell lines and 480-630 bases upstream in colchicine-selected cell lines. Southern hybridization analyses with different portions of a full-length cDNA indicate that the human mdr1 gene encompasses at least 70 kilobases of DNA amplified in all highly multidrug-resistant cell lines.

摘要

对秋水仙碱、长春碱或阿霉素产生耐药性的人KB癌细胞中的多药耐药性是由一个特定基因(mdr1)的过度表达以及频繁扩增所导致的。从多药耐药的KB细胞中已经获得了表示完整4.7千碱基mdr1转录本的重叠cDNA克隆。引物延伸和S1核酸酶保护实验表明,在所有人类多药耐药细胞系中,有两个转录本在第一个ATG密码子上游136和140个碱基处起始。mdr1基因在人类正常肾细胞和HepG2肝细胞中作为从相同位点起始的多聚腺苷酸化RNA进行表达。在长春碱或阿霉素选择的细胞系中,发现不太明显的转录本在第一个ATG密码子上游155 - 180个碱基处起始,而在秋水仙碱选择的细胞系中则在第一个ATG密码子上游480 - 630个碱基处起始。用全长cDNA的不同部分进行的Southern杂交分析表明,人类mdr1基因包含至少70千碱基的DNA,在所有高度多药耐药细胞系中均有扩增。

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