Yang Li, Chen Jiang, Chang Catherine C Y, Yang Xin-Ying, Wang Zhen-Zhen, Chang Ta-Yuan, Li Bo-Liang
State Key Laboratory of Molecular Biology, Institute of Biochemistry and Cell Biology, Shanghai Institutes for Biological Sciences, the Chinese Academy of Sciences.
Acta Biochim Biophys Sin (Shanghai). 2004 Apr;36(4):259-68. doi: 10.1093/abbs/36.4.259.
Human ACAT 1 cDNA K1 was first cloned and functionally expressed in 1993. There are two adjacent in-frame AUG codons, AUG(1397-1399) and AUG(1415-1417), at 5'-terminus of the open reading frame (ORF, nt 1397-3049) of human ACAT1 mRNA corresponding to cDNA K1. In current work, these two adjacent inframe AUGs at 5'-terminus of the predicted ORF (5'-ORF-AUGs) as start codons for translation initiation of human ACAT1 mRNA were characterized in detail. Codon mutations indicated that both of these two adjacent 5'-ORF-AUGs can be selected as start codons but the first 5'-ORF-AUG(1397-1399) is a main start codon consistent with that of the predicted ORF of human ACAT1 mRNA. Further deletion and mutation analyses demonstrated that a stable upstream stem-loop structure enhanced the selection of the first 5'-ORF-AUG(1397 -1399) as a main start codon, in addition to upstream nucleotide A in the -3 position, which is a key site of Kozak sequence. In addition, result of ACAT1 enzymatic activity assay showed no obvious difference between these two ACAT1 proteins respectively initiated from the two adjacent 5'-ORF-AUGs. This work showed that a stable upstream stem-loop structure could modulate the start codon selection during translation initiation of mRNAs that contain adjacent multi-5'-ORF-AUGs.
人ACAT 1 cDNA K1于1993年首次被克隆并实现功能表达。在与人ACAT1 mRNA的cDNA K1相对应的开放阅读框(ORF,核苷酸1397 - 3049)的5'端,有两个相邻的符合读框的AUG密码子,即AUG(1397 - 1399)和AUG(1415 - 1417)。在当前工作中,对这两个位于预测ORF 5'端的相邻读框内AUG(5'-ORF-AUGs)作为人ACAT1 mRNA翻译起始的起始密码子进行了详细表征。密码子突变表明,这两个相邻的5'-ORF-AUGs都可以被选作起始密码子,但第一个5'-ORF-AUG(1397 - 1399)是与人ACAT1 mRNA预测ORF一致的主要起始密码子。进一步的缺失和突变分析表明,除了-3位置的上游核苷酸A(这是科扎克序列的关键位点)外,一个稳定的上游茎环结构增强了第一个5'-ORF-AUG(1397 - 1399)作为主要起始密码子的选择。此外,ACAT1酶活性测定结果显示,分别由这两个相邻的5'-ORF-AUGs起始的这两种ACAT1蛋白之间没有明显差异。这项工作表明,一个稳定的上游茎环结构可以在含有相邻多个5'-ORF-AUGs的mRNA翻译起始过程中调节起始密码子的选择。