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Recoding elements located adjacent to a subset of eukaryal selenocysteine-specifying UGA codons

机译:位于与真核硒代半胱氨酸特异性UGA密码子的子集相邻的编码元件

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摘要

Incorporation of the 21st amino acid, selenocysteine, into proteins is specified in all three domains of life by dynamic translational redefinition of UGA codons. In eukarya and archaea, selenocysteine insertion requires a cis-acting selenocysteine insertion sequence (SECIS) usually located in the 3′UTR of selenoprotein mRNAs. Here we present comparative sequence analysis and experimental data supporting the presence of a second stop codon redefinition element located adjacent to a selenocysteine-encoding UGA codon in the eukaryal gene, SEPN1. This element is sufficient to stimulate high-level (6%) translational redefinition of the SEPN1 UGA codon in human cells. Readthrough levels further increased to 12% when tested in the presence of the SEPN1 3′UTR SECIS. Directed mutagenesis and phylogeny of the sequence context strongly supports the importance of a stem loop starting six nucleotides 3′ of the UGA codon. Sequences capable of forming strong RNA structures were also identified 3′ adjacent to, or near, selenocysteine-encoding UGA codons in the Sps2, SelH, SelO, and SelT selenoprotein genes.
机译:通过UGA密码子的动态翻译重新定义,在生命的所有三个域中都指定了将第21个氨基酸硒代半胱氨酸掺入蛋白质。在真核生物和古细菌中,硒代半胱氨酸插入需要一个顺式作用的硒代半胱氨酸插入序列(SECIS),通常位于硒蛋白mRNA的3'UTR中。在这里,我们介绍比较序列分析和实验数据,支持在真核基因SEPN1中与硒代半胱氨酸编码UGA密码子相邻的第二个终止密码子重定义元素的存在。此元素足以刺激人细胞中SEPN1 UGA密码子的高水平(6%)翻译重新定义。在SEPN1 3'UTR SECIS存在下进行测试时,通读水平进一步提高到12%。序列背景的定向诱变和系统发生学强烈支持了从UGA密码子3个核苷酸的6个核苷酸开始的茎环的重要性。还在Sps2,SelH,SelO和SelT硒蛋白基因中的编码硒代半胱氨酸的UGA密码子的3'附近或附近鉴定了能够形成强RNA结构的序列。

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