Suppr超能文献

人甲状腺髓样癌细胞系中胃饥饿素基因启动子区域的鉴定

Identification of promoter region of ghrelin gene in human medullary thyroid carcinoma cell line.

作者信息

Nakai Naoya, Kaneko Masabumi, Nakao Nobuhiro, Fujikawa Takahiko, Nakashima Kunio, Ogata Masato, Tanaka Minoru

机构信息

Department of Biochemistry, Faculty of Medicine, Mie University, 2-174 Edobashi, Tsu, Mie 514-8507, Japan.

出版信息

Life Sci. 2004 Sep 17;75(18):2193-201. doi: 10.1016/j.lfs.2004.04.028.

Abstract

Ghrelin, an endogenous ligand for growth hormone (GH) secretagogue receptor, stimulates GH secretion. The ghrelin gene is expressed most abundantly in stomach. The mRNA is also detected in other tissues and cell lines. However, the mechanism of the transcriptional regulation of the ghrelin gene has not yet been clarified. In the present study, we have investigated the regulatory region of the ghrelin gene expression in the human medullary thyroid carcinoma cell line (TT cells). PCR analysis of the 5'-region for human ghrelin gene revealed the presence of the first exon corresponding to the short non-coding first exon of the mouse ghrelin gene. The first exon is located at the 502 bp upstream from the 5'-end of the formerly reported human ghrelin gene. RT-PCR analysis showed the expression of the first exon in the stomach and TT cells. The expression of the first exon in the human stomach was confirmed by 5'-RACE method. Significant level of promoter activity was observed in the 1225-1107 bp up-stream region of the translation initiation site by luciferase assay. Specific protein binding to the promoter region of -1129 to -1100 was detected by electrophoretic mobility shift assay with nuclear extract from TT cells. These results suggest that the ghrelin gene expression in TT cells might be regulated by the upstream region of the first exon.

摘要

胃饥饿素是生长激素(GH)促分泌素受体的内源性配体,可刺激GH分泌。胃饥饿素基因在胃中表达最为丰富。在其他组织和细胞系中也可检测到该基因的mRNA。然而,胃饥饿素基因转录调控的机制尚未阐明。在本研究中,我们调查了人甲状腺髓样癌细胞系(TT细胞)中胃饥饿素基因表达的调控区域。对人胃饥饿素基因5'-区域的PCR分析显示,存在与小鼠胃饥饿素基因短的非编码第一外显子相对应的第一外显子。该第一外显子位于先前报道的人胃饥饿素基因5'-末端上游502 bp处。RT-PCR分析表明第一外显子在胃和TT细胞中表达。通过5'-RACE方法证实了第一外显子在人胃中的表达。通过荧光素酶测定法在翻译起始位点上游1225 - 1107 bp区域观察到显著水平的启动子活性。用TT细胞核提取物进行电泳迁移率变动分析检测到与-1129至-1100启动子区域特异性结合的蛋白质。这些结果表明,TT细胞中胃饥饿素基因的表达可能受第一外显子上游区域的调控。

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