Okamura S, Ng C C, Koyama K, Takei Y, Arakawa H, Monden M, Nakamura Y
Human Genome Center, Institute of Medical Science, The University of Tokyo, Japan.
Oncol Res. 1999;11(6):281-5.
We applied a differential display method to screen mRNAs isolated from a newly established cell line that carried a wild-type p53 transgene under control of the lactose operon. To investigate the p53 signaling pathway, we looked for genes whose expression was significantly induced or suppressed by induction of wild-type p53 protein, and identified seven. DNA sequence analyses revealed that the two genes that were upregulated encoded isozyme 6 of aldehyde dehydrogenase (ALDH6) and subunit I of cytochrome c oxidase (COI). The five genes that were downregulated encoded protein-tyrosine kinase (Syk), high mobility group chromosomal protein 17 (HMG-17), transferrin receptor, human alpha-tubulin, and sds22-like protein. The results indicated that genes related to cell cycle regulation, cell respiration, and cytoskeletal structure are involved in the process of growth arrest induced by wild-type p53.
我们应用差异显示方法筛选从一个新建立的细胞系中分离出的mRNA,该细胞系携带在乳糖操纵子控制下的野生型p53转基因。为了研究p53信号通路,我们寻找那些其表达被野生型p53蛋白的诱导显著诱导或抑制的基因,并鉴定出了7个。DNA序列分析表明,上调的两个基因编码醛脱氢酶6(ALDH6)同工酶6和细胞色素c氧化酶亚基I(COI)。下调的五个基因编码蛋白酪氨酸激酶(Syk)、高迁移率族染色体蛋白17(HMG-17)、转铁蛋白受体、人α-微管蛋白和sds22样蛋白。结果表明,与细胞周期调控、细胞呼吸和细胞骨架结构相关的基因参与了野生型p53诱导的生长停滞过程。