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阿霉素耐药的P388小鼠白血病细胞中DNA拓扑异构酶II基因突变等位基因的证据。

Evidence for a mutant allele of the gene for DNA topoisomerase II in adriamycin-resistant P388 murine leukemia cells.

作者信息

Deffie A M, Bosman D J, Goldenberg G J

机构信息

Manitoba Institute of Cell Biology, University of Manitoba, Winnipeg, Canada.

出版信息

Cancer Res. 1989 Dec 15;49(24 Pt 1):6879-82.

PMID:2555055
Abstract

Previous studies have shown that DNA topoisomerase II enzyme activity and protein levels are reduced in cloned lines of Adriamycin-resistant P388 leukemia cells relative to drug-sensitive cells (Deffie et al., Cancer Res., 49: 58-62, 1989). The molecular basis of the reduced topoisomerase II levels in these resistant cells has been investigated. Northern blot analysis of total cellular RNA from drug-sensitive and -resistant cells using a 1.8-kilobase human topoisomerase II complementary DNA revealed the presence of two mRNA species: a 6.6-kilobase transcript that was strongly expressed in drug-sensitive cells but reduced 7- to 8-fold in resistant cells; and a 5.5-kilobase transcript detected only in drug-resistant cells. Southern blot analysis of genomic DNA digested with BamHI, StuI, or PvuII and probed with the 1.8-kilobase complementary DNA for human topoisomerase II showed that, in Adriamycin-resistant cells, there were two different alleles for topoisomerase II, one identical to the native allele but with a lower gene copy number than that found in sensitive cells, and a second allele containing a mutation present only in resistant cells. These findings suggest that the reduced levels of topo II protein in drug-resistant cells may be due to reduced amounts of the native 6.6-kilobase mRNA. The unique 5.5-kilobase mRNA in resistant cells may represent a shortened transcript of the mutated topoisomerase II allele.

摘要

先前的研究表明,与阿霉素敏感的细胞相比,阿霉素抗性的P388白血病细胞克隆系中的DNA拓扑异构酶II的酶活性和蛋白质水平降低(Deffie等人,《癌症研究》,49:58 - 62,1989)。已经对这些抗性细胞中拓扑异构酶II水平降低的分子基础进行了研究。使用1.8千碱基的人拓扑异构酶II互补DNA对药物敏感和抗性细胞的总细胞RNA进行Northern印迹分析,发现存在两种mRNA种类:一种6.6千碱基的转录本,在药物敏感细胞中强烈表达,但在抗性细胞中减少了7至8倍;以及一种仅在抗性细胞中检测到的5.5千碱基的转录本。用BamHI、StuI或PvuII消化基因组DNA并用1.8千碱基的人拓扑异构酶II互补DNA进行Southern印迹分析表明,在阿霉素抗性细胞中,拓扑异构酶II有两种不同的等位基因,一种与天然等位基因相同,但基因拷贝数比敏感细胞中的低,另一种等位基因含有仅在抗性细胞中存在的突变。这些发现表明,抗性细胞中拓扑异构酶II蛋白水平的降低可能是由于天然6.6千碱基mRNA的量减少。抗性细胞中独特的5.5千碱基mRNA可能代表突变的拓扑异构酶II等位基因的缩短转录本。

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