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1型人类免疫缺陷病毒整合酶在体内稳定线性化的HIV-1长末端重复序列质粒。

Human immunodeficiency virus type 1 integrase stabilizes a linearized HIV-1 LTR plasmid in vivo.

作者信息

Faust E A, Acel A, Udashkin B, Wainberg M A

机构信息

Lady Davis Institute for Medical Research, SMBD-Jewish General Hospital, Montreal, Quebec, Canada.

出版信息

Biochem Mol Biol Int. 1995 Jul;36(4):745-58.

PMID:8528137
Abstract

A mammalian expression vector designed for production of HIV-1 integrase was found to enhance the stability of a linear reporter plasmid in COS-7 cells. The effect is strictly dependent on coexpression of the HIV-1 rev gene and on the inclusion of U3 and U5 portions of the HIV-1 LTR in the reporter plasmid. Integrase point mutations P109S and D116N drastically reduced stabilization whereas T115A and D64A had little or no effect. Immunoblot analysis revealed the presence of a 32-34kDa integrase protein in extracts of transfected COS-7 cells and of wild type and mutant integrase proteins at comparable levels. We conclude that integrase acts in trans in COS-7 cells, possibly by binding to the HIV-1 LTR in the plasmid. This transfection system may be useful for studying factors that stabilize the HIV-1 DNA genome prior to its integration into the host cell chromosome.

摘要

一种设计用于生产HIV-1整合酶的哺乳动物表达载体被发现可增强线性报告质粒在COS-7细胞中的稳定性。该效应严格依赖于HIV-1 rev基因的共表达以及报告质粒中HIV-1长末端重复序列(LTR)的U3和U5部分的存在。整合酶点突变P109S和D116N显著降低了稳定性,而T115A和D64A几乎没有影响或没有影响。免疫印迹分析显示,在转染的COS-7细胞提取物中存在一种32 - 34kDa的整合酶蛋白,野生型和突变型整合酶蛋白水平相当。我们得出结论,整合酶在COS-7细胞中发挥反式作用,可能是通过与质粒中的HIV-1 LTR结合。这种转染系统可能有助于研究在HIV-1 DNA基因组整合到宿主细胞染色体之前稳定它的因素。

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