Donohue P J, Feng S L, Alberts G F, Guo Y, Peifley K A, Hsu D K, Winkles J A
Department of Molecular Biology, Holland Laboratory, American Red Cross, Rockville, MD 20855, USA.
Biochem J. 1996 Oct 1;319 ( Pt 1)(Pt 1):9-12. doi: 10.1042/bj3190009.
Polypeptide growth factors promote cell-cycle progression in part by the transcriptional activation of a diverse group of specific genes. We have used an mRNA differential-display approach to identify several fibroblast growth factor (FGF)-1 (acidic FGF)-inducible genes in NIH 3T3 cells. Here we report that one of these genes, called FGF-regulated (FR)-3, is predicted to encode G/T mismatch-binding protein (GTBP), a component of the mammalian DNA mismatch correction system. The murine GTBP gene is transiently expressed after FGF-1 or calf serum treatment, with maximal mRNA levels detected at 12 and 18 h post-stimulation. FGF-1-stimulated NIH 3T3 cells also express an increased amount of GTBP as determined by immunoblot analysis. These results indicate that elevated levels of GTBP may be required during the DNA synthesis phase of the cell cycle for efficient G/T mismatch recognition and repair.
多肽生长因子部分通过转录激活多种特定基因来促进细胞周期进程。我们利用mRNA差异显示方法在NIH 3T3细胞中鉴定出几个成纤维细胞生长因子(FGF)-1(酸性FGF)诱导基因。在此我们报告,这些基因之一,称为FGF调节(FR)-3,预计编码G/T错配结合蛋白(GTBP),它是哺乳动物DNA错配校正系统的一个组成部分。FGF-1或小牛血清处理后,小鼠GTBP基因瞬时表达,在刺激后12和18小时检测到最大mRNA水平。通过免疫印迹分析确定,FGF-1刺激的NIH 3T3细胞也表达增加量的GTBP。这些结果表明,在细胞周期的DNA合成阶段可能需要升高的GTBP水平以实现有效的G/T错配识别和修复。