Miyamoto S, Chiorini J A, Urcelay E, Safer B
Molecular Hemaatology Branch, NHLBI, Bethesda, MD 20892-1654, USA.
Biochem J. 1996 May 1;315 ( Pt 3)(Pt 3):791-8. doi: 10.1042/bj3150791.
Gene expression of the alpha-subunit of eukaryotic initiation factor-2 (eIF-2 alpha), involves transcriptional and post-transcriptional mechanisms. eIF-2 alpha is a single-copy gene expressing two mRNAs, 1.6 and 4.2 kb in size. Cloning and sequencing of the cDNA for the 4.2 kb mRNA revealed that it is the result of alternative polyadenylation site selection. Four polyadenylation sites were identified within the 3' untranslated region (UTR) of eIF-2 alpha, only two of which are normally utilized in human and mouse tissues. A functional role for the extended 3' UTR was assessed by comparing the translatability and stability of the 1.6 and 4.2 kb mRNAs. Both the 1.6 and 4.2 kb transcripts could be translated in vitro and were identified in vivo as being distributed on large polyribosomes. This indicates that both mRNAs are efficiently translated. Stability studies showed that in activated T-cells the 4.2 kb mRNA was more stable than the 1.6 kb mRNA. Polyadenylation site selection and mRNA stability differ for the two mRNAs of eIF-2 alpha. These activities might be modulated by sequence elements contained within the untranslated regions of the eIF-2 alpha gene.
真核起始因子2α亚基(eIF-2α)的基因表达涉及转录和转录后机制。eIF-2α是一个单拷贝基因,表达两种大小分别为1.6 kb和4.2 kb的mRNA。对4.2 kb mRNA的cDNA进行克隆和测序发现,这是选择性聚腺苷酸化位点选择的结果。在eIF-2α的3'非翻译区(UTR)内鉴定出四个聚腺苷酸化位点,其中只有两个在人和小鼠组织中正常使用。通过比较1.6 kb和4.2 kb mRNA的可翻译性和稳定性来评估延长的3'UTR的功能作用。1.6 kb和4.2 kb的转录本在体外均可翻译,并且在体内被鉴定为分布在大型多核糖体上。这表明两种mRNA均能有效翻译。稳定性研究表明,在活化的T细胞中,4.2 kb mRNA比1.6 kb mRNA更稳定。eIF-2α的两种mRNA的聚腺苷酸化位点选择和mRNA稳定性不同。这些活性可能受eIF-2α基因非翻译区内所含序列元件的调节。