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首页> 外文期刊>Genomics >The human elongation factor 1 A-2 gene (EEF1A2): complete sequence and characterization of gene structure and promoter activity.
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The human elongation factor 1 A-2 gene (EEF1A2): complete sequence and characterization of gene structure and promoter activity.

机译:人类延伸因子1 A-2基因(EEF1A2):基因结构和启动子活性的完整序列和特征。

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摘要

The eukaryotic elongation factor 1 A (eEF1A, formerly EF1alpha) is a key factor in protein synthesis, where it promotes the transfer of aminoacylated tRNAs to the A site of the ribosome. Two differentially expressed isoforms of eEF1A, designated eEF1A-1 and eEF1A-2, are found in mammals. Here we report the isolation and sequencing of the gene (HGMW-approved symbol EEF1A2) coding for the human eEF1A-2 isoform. Furthermore, we characterize the gene structure and the activity of the promoter. Isolation of overlapping clones from human libraries revealed that the human eEF1A-2 gene spans approximately 10 kb and consists of eight exons. The intron-exon boundaries of human EEF1A2 and EEF1A1 are conserved, yet the gene of the eEF1A-2 isoform is larger than the eEF1A-1 gene because of enlarged introns. Primer extension analysis identified the predominant transcription start site 166 bp upstream of the AUG codon. The start site maps to an adenine located within a consensus initiator element. Sequencing of a 2-kb 5'-flanking promoter region revealed no TATA element. However, several putative cis-regulatory elements were discovered. The 5'-promoter activity was characterized by transient transfection experiments. Progressive deletions of the upstream promoter region defined a minimal promoter region, ranging from -16 to +92, that is sufficient to drive transcription. Copyright 2000 Academic Press.
机译:真核生物延伸因子1A(eEF1A,前身为EF1alpha)是蛋白质合成中的关键因素,它促进了氨基酰化的tRNA向核糖体A位点的转移。在哺乳动物中发现了两个eEF1A的差异表达同工型,分别称为eEF1A-1和eEF1A-2。在这里,我们报告编码和编码人类eEF1A-2亚型的基因(HGMW批准的符号EEF1A2)的分离和测序。此外,我们表征了基因结构和启动子的活性。从人文库中分离出重叠克隆后发现,人eEF1A-2基因跨度约为10 kb,由八个外显子组成。人类EEF1A2和EEF1A1的内含子-外显子边界是保守的,但由于内含子的扩大,eEF1A-2同工型的基因比eEF1A-1基因大。引物延伸分析确定了AUG密码子上游166 bp的主要转录起始位点。起始位点映射到位于共有启动子元素内的腺嘌呤。 2kb 5'侧翼启动子区的测序表明没有TATA元件。然而,发现了几种假定的顺式调控元件。通过瞬时转染实验来表征5'启动子活性。上游启动子区域的逐步删除定义了一个最小的启动子区域,范围从-16到+92,足以驱动转录。版权所有2000学术出版社。

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