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利用生物发光报告基因可视化活体哺乳动物中的基因表达。

Visualizing gene expression in living mammals using a bioluminescent reporter.

作者信息

Contag C H, Spilman S D, Contag P R, Oshiro M, Eames B, Dennery P, Stevenson D K, Benaron D A

机构信息

Department of Pediatrics, Stanford University School of Medicine, CA 94305-5119, USA.

出版信息

Photochem Photobiol. 1997 Oct;66(4):523-31. doi: 10.1111/j.1751-1097.1997.tb03184.x.

Abstract

Control of gene expression often involves an interwoven set of regulatory processes. As information regarding regulatory pathways may be lost in ex vivo analyses, we used bioluminescence to monitor gene expression in living mammals. Viral promoters fused to firefly luciferase as transgenes in mice allowed external monitoring of gene expression both superficially and in deep tissues. In vivo bioluminescence was detectable using either intensified or cooled charge-coupled device cameras, and could be detected following both topical and systemic delivery of substrate. In vivo control of the promoter from the human immunodeficiency virus was demonstrated. As a model for DNA-based therapies and vaccines, in vivo transfection of a luciferase expression vector (SV-40 promoter and enhancer controlling expression) was detected. We conclude that gene regulation, DNA delivery and expression can now be noninvasively monitored in living mammals using a luciferase reporter. Thus, real-time, noninvasive study of gene expression in living animal models for human development and disease is possible.

摘要

基因表达的调控通常涉及一系列相互交织的调节过程。由于有关调节途径的信息可能在体外分析中丢失,我们利用生物发光来监测活体哺乳动物中的基因表达。在小鼠中,与萤火虫荧光素酶融合的病毒启动子作为转基因,可对浅表和深部组织中的基因表达进行外部监测。使用增强型或冷却型电荷耦合器件相机可检测体内生物发光,在局部和全身递送底物后均可检测到。已证明可在体内控制来自人类免疫缺陷病毒的启动子。作为基于DNA的治疗和疫苗的模型,检测到荧光素酶表达载体(由SV-40启动子和增强子控制表达)的体内转染。我们得出结论,现在可以使用荧光素酶报告基因在活体哺乳动物中对基因调控、DNA递送和表达进行非侵入性监测。因此,在用于人类发育和疾病的活体动物模型中对基因表达进行实时、非侵入性研究是可能的。

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