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首页> 外文期刊>Nucleic Acids Research >Importance of the conserved nucleotides around the tRNA-like structure of Escherichia coli transfer-messenger RNA for protein tagging
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Importance of the conserved nucleotides around the tRNA-like structure of Escherichia coli transfer-messenger RNA for protein tagging

机译:大肠杆菌转移信使RNA的tRNA样结构周围保守核苷酸对蛋白质标签的重要性

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A bacterial RNA functioning as both tRNA and mRNA, transfer-messenger RNA (tmRNA) rescues stalled ribosomes and clears the cell of incomplete polypeptides. For function, Escherichia coli tmRNA requires an elaborate interplay between a tRNA-like structure and an internal mRNA domain that are connected by a 295 nt long compact secondary structure. The tRNA-like structure is surrounded by 16 unpaired nt, including 10 residues that are >95% conserved among the known 140 tmRNA sequences. All these residues were mutated to define their putative role(s) in trans-translation. Both the extent of aminoacylation and the alanine incorporation into the tag sequence, reflecting the two functions of tmRNA, were measured in vitro for all variants. As anticipated from the low sequence conservation, mutating positions 8-12 and position 15 affects neither aminoacylation nor protein tagging. Mutating a set of two conserved positions 13 and 14 abolishes both functions. probing the solution conformation indicates that this defective mutant adopts an alternate conformation of its acceptor stem that is no more aminoacylatable, and thus inactive in protein tagging. Selected point mutations at the conserved nucleotide stretches 16-20 and 333-335 seriously impair protein tagging with only minor changes in their solution conformations and aminoacylation. Point mutations at conserved positions 19 and 334 abolish trans-translation and 70S ribosome binding, although retaining nearly normal aminoacylation capacities. Two proteins that are known to interact with tmRNA were purified, and their interactions with the defective RNA variants were examined in vitro. Based on phylogenetic and functional data, an additional structural motif consisting of a quartet composed of non-Watson-Crick base pairs 5'-YGAC-3':5'-GGAC-5' involving some of the conserved nucleotides new to the tRNA-like portion is proposed. Overall, the highly conserved nucleotides around the tRNA-like portion are maintained for both structural and functional requirements during evolution.
机译:传递信使RNA(tmRNA)是一种既充当tRNA又充当mRNA的细菌RNA,可以拯救停滞的核糖体并清除细胞中不完整的多肽。为了发挥功能,大肠杆菌tmRNA需要通过295 nt长的紧凑二级结构连接的tRNA样结构与内部mRNA结构域之间的精细相互作用。 tRNA样结构被16个未配对的nt包围,包括10个在已知的140个tmRNA序列中> 95%保守的残基。将所有这些残基突变以定义其在反翻译中的假定作用。体外测量所有变体的氨基酰化程度和丙氨酸掺入标签序列,反映了tmRNA的两种功能。如从低序列保守性所预期的,突变位置8-12和位置15既不影响氨基酰化也不影响蛋白质标记。使一组两个保守位置13和14突变将消除这两个功能。探测溶液构象表明该缺陷突变体采用了其受体茎的替代构象,该构象不再具有氨基酰化能力,因此在蛋白质标记中无活性。在保守的核苷酸序列16-20和333-335上选择的点突变严重损害了蛋白质标记,其溶液构象和氨基酰化仅有很小的变化。尽管保留了几乎正常的氨酰化能力,但保守的19和334位点的点突变消除了反式翻译和70S核糖体结合。纯化了已知与tmRNA相互作用的两种蛋白质,并在体外检查了它们与缺陷RNA变体的相互作用。根据系统发育和功能数据,由由非Watson-Crick碱基对5'-YGAC-3':5'-GGAC-5'组成的四重奏组成的附加结构基序,涉及tRNA-新的一些保守核苷酸提出了类似的部分。总体而言,在进化过程中,tRNA样部分周围的高度保守的核苷酸可满足结构和功能需求。

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