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诺维科夫肝癌细胞核仁的扩增DNA以7.3千碱基的串联重复序列排列。

Amplified DNA of the Novikoff hepatoma nucleolus is arranged in a 7.3-kilobase tandem repeat.

作者信息

Parker D L, Mroczka D L, Rothblum L I

出版信息

Biochemistry. 1985 Jul 16;24(15):4229-33. doi: 10.1021/bi00336a062.

Abstract

We have reported previously the cloning and characterization of a nucleolar-localized 5.8-kilobase (kb) EcoRI fragment that is approximately 50-fold more highly reiterated in Novikoff hepatoma tumor cells than in normal rat liver [Parker, D. L., Busch, H., & Rothblum, L. I. (1981) Biochemistry 20, 762]. In the present study, the arrangement of these 5.8-kb EcoRI segments within the Novikoff hepatoma genome was investigated. Through the use of "indirect" restriction site mapping, partial restriction enzyme digestions, and molecular cloning, we have determined that the 5.8-kb EcoRI fragment and a 1.5-kb EcoRI fragment together constitute a 7.3-kb unit. The 7.3-kb unit is present in the hepatoma genome as a tandem repeat and constitutes the unit of the DNA that has been amplified. Studies on the arrangement of homologous sequences in the normal rat genome indicate that the amplified DNA may have been derived by a rearrangement and amplification of the nontranscribed spacer of the ribosomal DNA (rDNA) repeat.

摘要

我们先前报道过一个定位于核仁的5.8千碱基(kb)EcoRI片段的克隆及特性分析,该片段在诺维科夫肝癌肿瘤细胞中的重复频率比正常大鼠肝脏中高约50倍[帕克,D. L.,布施,H.,& 罗斯布卢姆,L. I.(1981年)《生物化学》20,762]。在本研究中,对诺维科夫肝癌基因组中这些5.8 kb EcoRI片段的排列进行了研究。通过使用“间接”限制性酶切位点图谱、部分限制性内切酶消化和分子克隆,我们确定5.8 kb EcoRI片段和一个1.5 kb EcoRI片段共同构成一个7.3 kb的单元。7.3 kb单元以串联重复的形式存在于肝癌基因组中,并且构成了已扩增的DNA单元。对正常大鼠基因组中同源序列排列的研究表明,扩增的DNA可能是由核糖体DNA(rDNA)重复序列的非转录间隔区重排和扩增而来。

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