首都医科大学学报 ›› 1996, Vol. 17 ›› Issue (2): 95-98.

• 论著 • 上一篇    下一篇

NIH3T3细胞不同增殖时相c-fos和c-jun癌基因表达的动态分析

谭信1, 彭安2, 王永潮2, 曾灵芳3   

  1. 1. 首都医科大学遗传学教研室;2. 北京师范大学生物系;3. 北京医科大学病理学教研室
  • 收稿日期:1995-09-29 修回日期:1900-01-01 出版日期:1996-04-15 发布日期:1996-04-15

The Analysis of c-fos and c-jun Oncogenes Expression in Different Phases of NIH3T3 Cell Cycle Progression

Tan Xin1, Peng An2, Wang Yongchao2, Zeng Lingfang3   

  1. 1. Department of Genetics, Capital University of Medical Sciences;2. Department of Biology, Beijing Normal University;3. Department of Pathology, Beijing Medical University
  • Received:1995-09-29 Revised:1900-01-01 Online:1996-04-15 Published:1996-04-15

摘要: NIH3T3细胞经血清刺激由静止期进入G1期,提取该期不同时相细胞的总体RNA,并提取同步化于G1、S、G2和M期细胞的总体RNA,分别与c-fos(2.1kb)和c-jun(1.8kb)基因探针进行斑点杂交。结果显示2个癌基因除了在血清刺激后1h都出现mRNA聚集高峰外,c-jun还在血清刺激后16h时出现第2个聚集峰,生长期细胞在细胞周期各时相均只有c-fos基因的少量表达,而c-jun在S期的表达量明显高于其他各期。说明c-fos和c-jun除了在细胞进入生长周期时发挥基因调控功能外,c-jun还可能在晚G1/S期产生作用,这种作用不需c-fos蛋白的参与。

关键词: c-fos癌基因, c-jun癌基因, 基因表达, 细胞周期

Abstract: NIH3T3 cells' total RNA was extracted at various lengths of time after the cells were induced to re-enter the cell cycle from quesent stage by serum stimulation and at G1,S,G2 and M phases synchronized by double thymidine block and colcemid block.These samples were then analyzed by dot hybridization to determine the levels of c-fos and c-jun mRNA.Our results show that the peaks of c-fos and c-jun mRNA accumulation were found at 1 h after serum stimulation.Besides,it shows a second c-jun mRNA accumulation peak at 16h after serum stimulation.For the continuous growing cells,c-fos was found to be in low expression in every phases of cell cycle,whereas c-jun was found to have a high level of expression in S phase.These results suggest that in addition to the associated function of c-fos and c-jun in cells which are entering cell cycle,c-jun protein may play a unique role in G1/S phase which does not need c-fos protein to cooperate with.

Key words: c-fos oncogene, c-jun oncogene, gene expression, cell cycle

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