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用于监测缺氧诱导因子1转录活性的基于病毒的报告系统。

Virus-based reporter systems for monitoring transcriptional activity of hypoxia-inducible factor 1.

作者信息

Razorenova O V, Ivanov A V, Budanov A V, Chumakov P M

机构信息

Department of Molecular Biology, Lerner Research Institute, The Cleveland Clinic Foundation, 9500 Euclid Avenue, Cleveland, OH, 44195, USA.

出版信息

Gene. 2005 Apr 25;350(1):89-98. doi: 10.1016/j.gene.2005.02.006.

Abstract

Being key regulator of oxygen homeostasis hypoxia-inducible factor 1 (HIF-1) plays significant roles in cancer progression as well as in cardiovascular diseases. The modulation of HIF-1alpha activity in vivo may represent a valuable therapeutic approach to these disorders. In order to monitor HIF-1 transcriptional activity, we have developed HIF-1alpha-responsive reporter constructs, in which lacZ gene expression is driven by minimal Hsp70 gene promoter or minimal immediate early promoter of cytomegalovirus (CMV) and a combination of hypoxia response elements from regulatory regions of PGK1, ENO1 and LDHA genes. For the efficient delivery to a wide variety of cell types we chose retroviral and lentiviral vectors as carriers of the reporter cassette. We demonstrate that the obtained reporter system i) has a high inducibility in response to treatments leading to HIF-1alpha activation, ii) shows upregulation in response to HIF-1 activation and downregulation following inhibition of HIF-1alpha expression by small interfering RNA, iii) follows the dynamics of endogenous HIF-1 target gene expression. The retrovirus- and lentivirus-based reporters can be used for high-throughput screening of HIF-1alpha modulators and for the study of crosstalk between HIF-1 and different related signal transduction pathways. Potential applications for the reporters are discussed.

摘要

缺氧诱导因子1(HIF-1)作为氧稳态的关键调节因子,在癌症进展以及心血管疾病中发挥着重要作用。体内HIF-1α活性的调节可能是治疗这些疾病的一种有价值的方法。为了监测HIF-1的转录活性,我们构建了HIF-1α反应性报告基因载体,其中lacZ基因的表达由最小热休克蛋白70(Hsp70)基因启动子或巨细胞病毒(CMV)的最小立即早期启动子以及来自磷酸甘油酸激酶1(PGK1)、烯醇化酶1(ENO1)和乳酸脱氢酶A(LDHA)基因调控区的缺氧反应元件组合驱动。为了有效地将报告基因载体递送至多种细胞类型,我们选择逆转录病毒和慢病毒载体作为报告基因盒的载体。我们证明,所获得的报告基因系统:i)对导致HIF-1α激活的处理具有高诱导性;ii)对HIF-1激活有上调反应,而在通过小干扰RNA抑制HIF-1α表达后则下调;iii)遵循内源性HIF-1靶基因表达的动态变化。基于逆转录病毒和慢病毒的报告基因可用于高通量筛选HIF-1α调节剂以及研究HIF-1与不同相关信号转导途径之间的相互作用。文中还讨论了该报告基因的潜在应用。

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