Woloschak G E, Shearin-Jones P, Chang-Liu C M
Biological and Medical Research Division, Argonne National Laboratory, Illinois 60439.
Mol Carcinog. 1990;3(6):374-8. doi: 10.1002/mc.2940030609.
We examined the modulation in expression of genes encoding three cytoskeletal elements (beta-actin, gamma-actin, and alpha-tubulin) in Syrian hamster embryo (SHE) cells following exposure to ionizing radiations. Early-passage SHE cells were irradiated in plateau phase with various low doses (12-200 cGy) of neutrons, gamma-rays, or x-rays. RNA samples were prepared from cells at different times postexposure and were analyzed for levels of specific transcripts by northern blots. The results revealed that alpha-tubulin was induced by both high-linear energy of transfer (LET) (neutrons) and low-LET (gamma-rays and x-rays) radiations with similar kinetics. The peak in alpha-tubulin mRNA accumulation occurred between 1 and 3 h postexposure; for gamma-actin mRNA, accumulation was similarly induced. For both gamma-actin and alpha-tubulin, the higher the dose during the first hour postexposure (up to 200 cGy gamma-rays), the greater the level of mRNA induction. In contrast, mRNA specific for beta-actin showed decreased accumulation during the first hour following radiation exposure, and remained low up to 3 h postexposure. These results document the differential modulation of genes specific for cytoskeletal elements following radiation exposure. In addition, they demonstrate a decrease in the ratio of beta-actin:gamma-actin mRNA within the first 3 h following gamma-ray exposure. These changes in mRNA accumulation are similar to those reported in some transformed cell lines and in cells treated with tumor promoters, which suggests a role for changes in actin- and tubulin-mRNA expression in radiation-mediated transformation.
我们研究了叙利亚仓鼠胚胎(SHE)细胞在暴露于电离辐射后,编码三种细胞骨架成分(β-肌动蛋白、γ-肌动蛋白和α-微管蛋白)的基因表达的调节情况。处于平台期的早期传代SHE细胞用各种低剂量(12 - 200 cGy)的中子、γ射线或X射线进行辐照。在暴露后的不同时间从细胞中制备RNA样本,并通过Northern印迹分析特定转录本的水平。结果显示,α-微管蛋白在高传能线密度(LET)(中子)和低LET(γ射线和X射线)辐射下均被诱导,且动力学相似。α-微管蛋白mRNA积累的峰值出现在暴露后1至3小时之间;γ-肌动蛋白mRNA的积累也以类似方式被诱导。对于γ-肌动蛋白和α-微管蛋白,暴露后第一小时内的剂量越高(γ射线高达200 cGy),mRNA诱导水平越高。相比之下,β-肌动蛋白特异性mRNA在辐射暴露后的第一小时内积累减少,并且在暴露后3小时内一直保持在低水平。这些结果证明了辐射暴露后细胞骨架成分特异性基因的差异调节。此外,它们还表明在γ射线暴露后的前3小时内,β-肌动蛋白:γ-肌动蛋白mRNA的比例降低。mRNA积累的这些变化与一些转化细胞系和用肿瘤启动子处理的细胞中报道的变化相似,这表明肌动蛋白和微管蛋白mRNA表达的变化在辐射介导的转化中起作用。