首页> 外文期刊>Nucleic Acids Research >INTERACTION OF THE ESCHERICHIA COLI FDHF MRNA HAIRPIN PROMOTING SELENOCYSTEINE INCORPORATION WITH THE RIBOSOME
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INTERACTION OF THE ESCHERICHIA COLI FDHF MRNA HAIRPIN PROMOTING SELENOCYSTEINE INCORPORATION WITH THE RIBOSOME

机译:大肠埃希氏菌FDHF MRNA Hairpin促进硒代半胱氨酸掺入与核糖体的相互作用

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The codon UGA located 5' adjacent to an mRNA hairpin within fdhF mRNA promotes the incorporation of the amino acid selenocysteine into formate dehydrogenase H of Escherichia coil, The loop region of this mRNA hairpin has been shown to bind to the special elongation factor SELB, which also forms a complex with selenocysteinyl-tRNA(Sec) and GTP, We designed seven different mRNA constructs derived from the fdhF mRNA which contain a translation initiation region including an AUG initiation codon followed by no, one, two, three, four, five or six UUC phenylalanine codon(s) and the UGA selenocysteine codon 5' adjacent to the fdhF mRNA hairpin, By binding these different mRNA constructs to 30S ribosomal subunits in vitro we attempted to mimic intermediate steps of elongation of a structured mRNA approaching the ribosome by one codon at a time, Toeprint analysis of the mRNA-ribosome complexes showed that the presence of the fdhF mRNA hairpin strongly interferes with binding of the fdhF mRNA to 30S ribosomal subunits as soon as the hairpin is placed closer than 16 bases to the ribosomal P-site, Binding is reduced up to 25-fold compared with mRNA constructs where the hairpin is located outside the ribosomal mRNA track. Surprisingly, no toeprint signals were observed in any of our mRNA constructs when tRNA(SeC) was used instead of tRNA(fMet). Lack of binding of selenocysteinyl-tRNA(SeC) to the UGA codon was attributed to steric hindrance by the fdhF mRNA hairpin, By chemical probing of the shortest mRNA construct (AUG-UGA-fdhF hairpin) bound to 30S ribosomal subunits we demonstrate that the hairpin structure is not unfolded in the presence of ribosomes in vitro; also, th is mRNA is not translated in vivo when fused in-frame 5' of the lacZ gene. Therefore, our data indicate that the fdhF mRNA hairpin has to be unfolded during elongation prior to entering the ribosomal mRNA track and we propose that the SELB binding domain within the fdhF mRNA is located outside the ribosomal mRNA track during decoding of the UGA selenocysteine codon by the SELB-selenocysteinyl tRNA(SeC)-GTP complex.
机译:位于fdhF mRNA中与mRNA发夹相邻的5'密码子UGA促进氨基酸硒代半胱氨酸掺入大肠埃希氏菌的甲酸脱氢酶H中。该mRNA发夹的环区已显示出与特殊的延伸因子SELB结合。还与硒代半胱氨酰-tRNA(Sec)和GTP形成复合物,我们设计了来自fdhF mRNA的七个不同的mRNA构建体,其中包含一个翻译起始区,包括一个AUG起始密码子,其后依次是no,1、2、3、4、5或与fdhF mRNA发夹相邻的6个UUC苯丙氨酸密码子和UGA硒代半胱氨酸密码子5',通过在体外将这些不同的mRNA构建体与30S核糖体亚基结合,我们试图模拟一个结构化的mRNA延伸接近核糖体的中间步骤密码子一次,对mRNA-核糖体复合物的脚印分析表明,fdhF mRNA发夹的存在强烈干扰了fdhF mRNA与一旦将发夹放置在距离核糖体P位点比16个碱基更近的位置,就会有30S核糖体亚基,与发夹位于核糖体mRNA轨道之外的mRNA构建体相比,结合减少了25倍。令人惊讶的是,当使用tRNA(SeC)代替tRNA(fMet)时,在我们的任何mRNA构建体中均未观察到脚印信号。硒代半胱氨酰-tRNA(SeC)缺乏与UGA密码子的结合归因于fdhF mRNA发夹的位阻。通过化学探测与30S核糖体亚基结合的最短mRNA构建体(AUG-UGA-fdhF发夹),我们证明了在体外存在核糖体时发夹结构不会展开;同样,当lacZ基因的框内5'融合时,mRNA在体内不翻译。因此,我们的数据表明,fdhF mRNA发夹在进入核糖体mRNA轨道之前必须在延伸过程中被解开,并且我们建议在通过UGA硒代半胱氨酸密码子的解码过程中,fdhF mRNA内的SELB结合域位于核糖体mRNA轨道之外。 SELB-硒代半胱氨酰tRNA(SeC)-GTP复合物。

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