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γ射线、紫外线辐射、阳光、微波及电磁场对由人类免疫缺陷病毒启动子介导的基因表达的影响

Effects of gamma rays, ultraviolet radiation, sunlight, microwaves and electromagnetic fields on gene expression mediated by human immunodeficiency virus promoter.

作者信息

Libertin C R, Panozzo J, Groh K R, Chang-Liu C M, Schreck S, Woloschak G E

机构信息

Center for Mechanistic Biology and Biotechnology, Argonne National Laboratory, Illinois 60439-4833.

出版信息

Radiat Res. 1994 Oct;140(1):91-6.

PMID:7938460
Abstract

Previous work by our group and others has shown the modulation of human immunodeficiency virus (HIV) promoter or long terminal repeat (LTR) after exposure to neutrons and ultraviolet radiations. Using HeLa cells stably transfected with a construct containing the chloramphenicol acetyl transferase (CAT) gene, the transcription of which is mediated by the HIV-LTR, we designed experiments to examine the effects of exposure to different types of radiation (such as gamma rays, ultraviolet and sunlight irradiations, electromagnetic fields and microwaves) on HIV-LTR-driven expression of CAT. These results demonstrated ultraviolet-light-induced transcription from the HIV promoter, as has been shown by others. Exposure to other DNA-damaging agents such as gamma rays and sunlight (with limited exposures) had no significant effect on transcription mediated by HIV-LTR, suggesting that induction of HIV is not mediated by just any type of DNA damage but rather may require specific types of DNA damage. Microwaves did not cause cell killing when cells in culture were exposed in high volumes of medium, and the same cells showed no changes in expression. When microwave exposure was carried out in low volumes of medium (so that excessive heat was generated) induction of HIV-LTR transcription (as assayed by CAT activity) was evident. Electromagnetic field exposures had no effect on expression of HIV-LTR. These results demonstrate that not all types of radiation and not all DNA-damaging agents are capable of inducing HIV. We hypothesize that induction of HIV transcription may be mediated by several different signals after exposure to radiation.

摘要

我们团队及其他人员之前的研究表明,人类免疫缺陷病毒(HIV)启动子或长末端重复序列(LTR)在受到中子和紫外线辐射后会发生调控。我们使用稳定转染了包含氯霉素乙酰转移酶(CAT)基因构建体的HeLa细胞,该基因的转录由HIV-LTR介导,设计实验来检测暴露于不同类型辐射(如γ射线、紫外线和阳光照射、电磁场和微波)对HIV-LTR驱动的CAT表达的影响。这些结果证明了紫外线诱导HIV启动子的转录,正如其他人所表明的那样。暴露于其他DNA损伤剂如γ射线和阳光(有限暴露)对HIV-LTR介导的转录没有显著影响,这表明HIV的诱导并非由任何类型的DNA损伤介导,而是可能需要特定类型的DNA损伤。当在大量培养基中暴露培养的细胞时,微波不会导致细胞死亡,并且相同的细胞在表达上没有变化。当在少量培养基中进行微波暴露(从而产生过多热量)时,HIV-LTR转录的诱导(通过CAT活性测定)很明显。电磁场暴露对HIV-LTR的表达没有影响。这些结果表明并非所有类型的辐射和并非所有DNA损伤剂都能够诱导HIV。我们推测,暴露于辐射后HIV转录的诱导可能由几种不同的信号介导。

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