Suppr超能文献

成纤维细胞生长因子-1对静止的NIH 3T3细胞的刺激会增加G/T错配结合蛋白的表达。

Fibroblast growth factor-1 stimulation of quiescent NIH 3T3 cells increases G/T mismatch-binding protein expression.

作者信息

Donohue P J, Feng S L, Alberts G F, Guo Y, Peifley K A, Hsu D K, Winkles J A

机构信息

Department of Molecular Biology, Holland Laboratory, American Red Cross, Rockville, MD 20855, USA.

出版信息

Biochem J. 1996 Oct 1;319 ( Pt 1)(Pt 1):9-12. doi: 10.1042/bj3190009.

Abstract

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.

摘要

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。

相似文献

本文引用的文献

1
Molecular cloning of the N-terminus of GTBP.GTBP N 端的分子克隆
Genomics. 1996 Feb 1;31(3):395-7. doi: 10.1006/geno.1996.0067.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验