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鸡延伸因子-2基因启动子区域的功能特性分析

Functional characterization of the promoter region of the chicken elongation factor-2 gene.

作者信息

Lim Eun Jin, Kim Choong Won

机构信息

Molecular and Cell Nutrition Laboratory, Department of Animal and Food Science, University of Kentucky, Lexington, Kentucky 40536, USA.

出版信息

Gene. 2007 Jan 15;386(1-2):183-90. doi: 10.1016/j.gene.2006.09.007. Epub 2006 Oct 3.

Abstract

Elongation factor 2 (EF-2) plays a key role in the essential process of protein synthesis by translocating tRNAs from the ribosomal A- and P-sites to the P- and E-sites. EF-2 regulates the outcome of protein synthesis in mammalian cells. This report demonstrates that chicken EF-2 protein levels are dependent on transcription in 8-bromo-cAMP, insulin and phorbol ester-treated cells. In order to delineate functional domains that control chicken EF-2 gene transcription, the 5'-flanking region of the chicken EF-2 promoter was analyzed. Deletion constructs from -550 and -86 had the same basal level promoter activity as the whole EF-2 promoter. The sequence between nucleotides -700 and -550 was determined to be a regulatory region for the chicken EF-2 basal promoter activity. The region between -700 and -550 has a negative regulatory region and two regulatory proteins (I, II). 8-bromo-cAMP increased chicken EF-2 promoter activity (-700/+102) in Rat 1 HIR fibroblast cells more than insulin and phorbol ester treatment. Binding of protein I and II were decreased by 8-bromo-cAMP but restored by a protein kinase A inhibitor (KT5720). GATA consensus sequence oligonucleotide and fragment -86/-50 prevented protein II binding of fragment -700/-550. This result suggested that protein II is a GATA-like protein. These observations provide a novel regulatory mechanism for the EF-2 promoter.

摘要

延伸因子2(EF-2)通过将tRNA从核糖体的A位点和P位点转运至P位点和E位点,在蛋白质合成这一关键过程中发挥着重要作用。EF-2调节哺乳动物细胞中蛋白质合成的结果。本报告表明,在经8-溴环磷酸腺苷、胰岛素和佛波酯处理的细胞中,鸡EF-2蛋白水平依赖于转录。为了确定控制鸡EF-2基因转录的功能结构域,对鸡EF-2启动子的5'侧翼区域进行了分析。从-550到-86的缺失构建体与整个EF-2启动子具有相同的基础水平启动子活性。核苷酸-700和-550之间的序列被确定为鸡EF-2基础启动子活性的调控区域。-700和-550之间的区域有一个负调控区域和两种调控蛋白(I、II)。在大鼠1 HIR成纤维细胞中,8-溴环磷酸腺苷比胰岛素和佛波酯处理更能提高鸡EF-2启动子活性(-700/+102)。8-溴环磷酸腺苷可降低蛋白I和II的结合,但蛋白激酶A抑制剂(KT5720)可使其恢复。GATA共有序列寡核苷酸和片段-86/-50可阻止片段-700/-550与蛋白II的结合。这一结果表明蛋白II是一种类GATA蛋白。这些观察结果为EF-2启动子提供了一种新的调控机制。

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