Lim Eun Jin, Kim Choong Won
Molecular and Cell Nutrition Laboratory, Department of Animal and Food Science, University of Kentucky, Lexington, Kentucky 40536, USA.
Gene. 2007 Jan 15;386(1-2):183-90. doi: 10.1016/j.gene.2006.09.007. Epub 2006 Oct 3.
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.
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。