Suppr超能文献

促进硒代半胱氨酸掺入的大肠杆菌fdhF mRNA发夹与核糖体的相互作用。

Interaction of the Escherichia coli fdhF mRNA hairpin promoting selenocysteine incorporation with the ribosome.

作者信息

Hüttenhofer A, Heider J, Böck A

机构信息

Lehrstuhl für Mikrobiologie der Universität München, Germany.

出版信息

Nucleic Acids Res. 1996 Oct 15;24(20):3903-10. doi: 10.1093/nar/24.20.3903.

Abstract

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 coli. 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, this 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.

摘要

位于fdhF mRNA内mRNA发夹结构5'端相邻位置的UGA密码子,可促使氨基酸硒代半胱氨酸掺入大肠杆菌甲酸脱氢酶H中。已证明该mRNA发夹结构的环区可与特殊延伸因子SELB结合,SELB还可与硒代半胱氨酰 - tRNA(Sec)和GTP形成复合物。我们设计了七种源自fdhF mRNA的不同mRNA构建体,它们包含一个翻译起始区域,该区域包括一个AUG起始密码子,后面跟着零个、一个、两个、三个、四个、五个或六个UUC苯丙氨酸密码子,以及位于fdhF mRNA发夹结构5'端相邻位置的UGA硒代半胱氨酸密码子。通过在体外将这些不同的mRNA构建体与30S核糖体亚基结合,我们试图模拟带有结构的mRNA每次以一个密码子的方式接近核糖体时延伸的中间步骤。对mRNA - 核糖体复合物的足迹分析表明,一旦fdhF mRNA发夹结构放置得比核糖体P位点近于16个碱基,它就会强烈干扰fdhF mRNA与30S核糖体亚基的结合。与发夹结构位于核糖体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足迹信号。硒代半胱氨酰 - tRNA(Sec)与UGA密码子缺乏结合归因于fdhF mRNA发夹结构的空间位阻。通过对与30S核糖体亚基结合的最短mRNA构建体(AUG - UGA - fdhF发夹结构)进行化学探测,我们证明在体外存在核糖体的情况下,发夹结构不会展开;此外,当该mRNA与lacZ基因的5'端读框融合时,它在体内也不会被翻译。因此,我们的数据表明,fdhF mRNA发夹结构在进入核糖体mRNA轨道之前的延伸过程中必须展开,并且我们提出在SELB - 硒代半胱氨酰 - tRNA(Sec) - GTP复合物对UGA硒代半胱氨酸密码子进行解码期间,fdhF mRNA内的SELB结合结构域位于核糖体mRNA轨道之外。

相似文献

引用本文的文献

本文引用的文献

10
Regulation of the synthesis of ribosomes and ribosomal components.核糖体及核糖体组分合成的调控。
Annu Rev Biochem. 1984;53:75-117. doi: 10.1146/annurev.bi.53.070184.000451.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验