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一组强拓扑异构酶II切割位点位于一个整合的人类免疫缺陷病毒附近。

A cluster of strong topoisomerase II cleavage sites is located near an integrated human immunodeficiency virus.

作者信息

Howard M T, Griffith J D

机构信息

Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill 27599.

出版信息

J Mol Biol. 1993 Aug 20;232(4):1060-8. doi: 10.1006/jmbi.1993.1460.

Abstract

The Human Immunodeficiency Virus (HIV) integrates into host cellular DNA as a double strand DNA molecule. Here a previously studied HIV isolate was examined for binding and cleavage by topoisomerase II in vitro within the 5' LTR region and human flanking DNA. A cluster of strong binding and cleavage sites in the human sequences was located approximately 850 bp upstream from the integration site. This region maps to a locus consisting of a complex repeating element, and alternating purine/pyrimidine sequences. Topoisomerase II binding and cleavage sites were also located within the HIV 5' LTR, in particular a site overlying the DNA sequence coding for TAR, another inverted repeat element in the DNA.

摘要

人类免疫缺陷病毒(HIV)作为双链DNA分子整合到宿主细胞DNA中。在此,对一种先前研究过的HIV分离株进行了检测,以观察其在体外5'长末端重复序列(LTR)区域和人类侧翼DNA内被拓扑异构酶II结合和切割的情况。人类序列中一组强结合和切割位点位于整合位点上游约850 bp处。该区域定位于一个由复杂重复元件和交替嘌呤/嘧啶序列组成的基因座。拓扑异构酶II结合和切割位点也位于HIV 5' LTR内,特别是一个覆盖编码TAR的DNA序列的位点,TAR是DNA中的另一个反向重复元件。

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