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The nature of the minimal 'selenocysteine insertion sequence' (SECIS) in Escherichia coli.

机译:大肠杆菌中最小的“硒代半胱氨酸插入序列”(SECIS)的性质。

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摘要

The UGA codon, usually a stop codon, can also direct the incorporation into a protein of the modified amino acid selenocysteine. This UGA decoding process requires a cis -acting mRNA element called 'selenocysteine insertion sequence' (SECIS) that can form a stem-loop structure. In Escherichia coli the SECIS of the selenoprotein formate dehydrogenase (FdhH) mRNA has been previously described to consist of at least 40 nucleotides following the UGA codon. Here we determined the nature of the minimal SECIS required for the in vivo UGA-directed selenocysteine incorporation in E.coli . Our study is based on extensive mutational analysis of the fdhF SECIS DNA located in a lac' Z fusion. We found that the whole stem-loop RNA structure of the E.coli fdhF SECIS previously described is not required for the UGA-directed selenocysteine incorporation in vivo . Rather, only its upper stem-loop structure of 17 nucleotides is necessary on the condition that it is located in a proper distance (11 nucleotides) from the UGA codon. Based on these observations, we present a new model for the minimal E.coli SECIS.
机译:UGA密码子,通常是终止密码子,也可以指导将修饰的氨基酸硒代半胱氨酸掺入蛋白质中。此UGA解码过程需要一个称为“硒代半胱氨酸插入序列”(SECIS)的顺式mRNA成分,该元件可以形成茎环结构。在大肠杆菌中,硒蛋白甲酸酯脱氢酶(FdhH)mRNA的SECIS先前已被描述为由UGA密码子后的至少40个核苷酸组成。在这里,我们确定了将体内UGA定向的硒代半胱氨酸掺入大肠杆菌所需的最低SECIS的性质。我们的研究基于位于lac'Z融合物中的fdhF SECIS DNA的广泛突变分析。我们发现,先前描述的大肠杆菌fdhF SECIS的整个茎环RNA结构对于在体内由UGA定向的硒代半胱氨酸掺入不是必需的。相反,仅在其距UGA密码子适当距离(11个核苷酸)的条件下,才需要其17个核苷酸的上部茎环结构。基于这些观察,我们提出了最小大肠杆菌SECIS的新模型。

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