Literature DB >> 9784370

In vitro selection of RNAs aminoacylated by Escherichia coli leucyl-tRNA synthetase.

H Asahara1, N Nameki, T Hasegawa.   

Abstract

To investigate systematically the RNA sequences necessary for aminoacylation by Escherichia coli leucyl-tRNA synthetase, RNAs with leucylation activity were isolated by in vitro selection from a library of tRNALeu variants possessing randomized sequences in the D-loop, the variable arm, and the T-loop. After two rounds of selection, most of the selected variants showed the following features: (1) the tertiary interaction between nucleotides at positions 15 and 48 was A15-U48; (2) the continuous G18G19 sequence, which is invariant in canonical tRNAs, appeared at the fixed position in the D-loop; and (3) the nucleotide at position 20a in the D-loop was A. These selected nucleotides and their positions, concentrating on the hinge region of tRNA, were identical to those of native tRNALeu. In contrast, although the long variable arm is the most characteristic of the tRNALeu structure, the primary and secondary structures were not correlated with the leucylation activity. These findings indicate that A15-U48, A20a, and G18G19 located at specific positions are involved in the tertiary folding of leucine-accepting tRNA molecules. With increases in the selection cycle, the D-loop sequence and the secondary structure of the variable arm became similar to those of tRNALeu, suggesting that tRNALeu represents an optimized RNA sequence for leucylation. Copyright 1998 Academic Press.

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Year:  1998        PMID: 9784370     DOI: 10.1006/jmbi.1998.2111

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  11 in total

1.  Tertiary structure base pairs between D- and TpsiC-loops of Escherichia coli tRNA(Leu) play important roles in both aminoacylation and editing.

Authors:  Xing Du; En-Duo Wang
Journal:  Nucleic Acids Res       Date:  2003-06-01       Impact factor: 16.971

2.  Two distinct domains of the beta subunit of Aquifex aeolicus leucyl-tRNA synthetase are involved in tRNA binding as revealed by a three-hybrid selection.

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Journal:  Nucleic Acids Res       Date:  2004-06-18       Impact factor: 16.971

3.  Novel genetic approach for in vivo vascular imaging in mice.

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4.  Identification of essential domains for Escherichia coli tRNA(leu) aminoacylation and amino acid editing using minimalist RNA molecules.

Authors:  Deana C Larkin; Amy M Williams; Susan A Martinis; George E Fox
Journal:  Nucleic Acids Res       Date:  2002-05-15       Impact factor: 16.971

5.  A T-stem slip in human mitochondrial tRNALeu(CUN) governs its charging capacity.

Authors:  Rui Hao; Ming-Wei Zhao; Zhan-Xi Hao; Yong-Neng Yao; En-Duo Wang
Journal:  Nucleic Acids Res       Date:  2005-06-22       Impact factor: 16.971

6.  In vitro selection to identify determinants in tRNA for Bacillus subtilis tyrS T box antiterminator mRNA binding.

Authors:  Hamid Fauzi; Karen D Jack; Jennifer V Hines
Journal:  Nucleic Acids Res       Date:  2005-05-06       Impact factor: 16.971

7.  Recognition of tRNALeu by Aquifex aeolicus leucyl-tRNA synthetase during the aminoacylation and editing steps.

Authors:  Peng Yao; Bin Zhu; Sophie Jaeger; Gilbert Eriani; En-Duo Wang
Journal:  Nucleic Acids Res       Date:  2008-03-26       Impact factor: 16.971

Review 8.  Mitochondrial transcript maturation and its disorders.

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Journal:  J Inherit Metab Dis       Date:  2015-05-28       Impact factor: 4.982

9.  The determination of tRNALeu recognition nucleotides for Escherichia coli L/F transferase.

Authors:  Angela Wai Shan Fung; Charles Chung Yun Leung; Richard Peter Fahlman
Journal:  RNA       Date:  2014-06-16       Impact factor: 4.942

10.  Crucial role of the C-terminal domain of Mycobacterium tuberculosis leucyl-tRNA synthetase in aminoacylation and editing.

Authors:  Qing-Hua Hu; Qian Huang; En-Duo Wang
Journal:  Nucleic Acids Res       Date:  2012-12-24       Impact factor: 16.971

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