Literature DB >> 10801348

tRNA leucine identity and recognition sets.

G Tocchini-Valentini1, M E Saks, J Abelson.   

Abstract

Transfer RNAs (tRNAs) are grouped into two classes based on the structure of their variable loop. In Escherichia coli, tRNAs from three isoaccepting groups are classified as type II. Leucine tRNAs comprise one such group. We used both in vivo and in vitro approaches to determine the nucleotides that are required for tRNA(Leu) function. In addition, to investigate the role of the tRNA fold, we compared the in vivo and in vitro characteristics of type I tRNA(Leu) variants with their type II counterparts.A minimum of six conserved tRNA(Leu) nucleotides were required to change the amino acid identity and recognition of a type II tRNA(Ser) amber suppressor from a serine to a leucine residue. Five of these nucleotides affect tRNA tertiary structure; the G15-C48 tertiary "Levitt base-pair" in tRNA(Ser) was changed to A15-U48; the number of nucleotides in the alpha and beta regions of the D-loop was changed to achieve the positioning of G18 and G19 that is found in all tRNA(Leu); a base was inserted at position 47n between the base-paired extra stem and the T-stem; in addition the G73 "discriminator" base of tRNA(Ser) was changed to A73. This minimally altered tRNA(Ser) exclusively inserted leucine residues and was an excellent in vitro substrate for LeuRS. In a parallel experiment, nucleotide substitutions were made in a glutamine-inserting type I tRNA (RNA(SerDelta); an amber suppressor in which the tRNA(Ser) type II extra-stem-loop is replaced by a consensus type I loop). This "type I" swap experiment was successful both in vivo and in vitro but required more nucleotide substitutions than did the type II swap. The type I and II swaps revealed differences in the contributions of the tRNA(Leu) acceptor stem base-pairs to tRNA(Leu) function: in the type I, but not the type II fold, leucine specificity was contingent on the presence of the tRNA(Leu) acceptor stem sequence. The type I and II tRNAs used in this study differed only in the sequence and structure of the variable loop. By altering this loop, and thereby possibly introducing subtle changes into the overall tRNA fold, it became possible to detect otherwise cryptic contributions of the acceptor stem sequence to recognition by LeuRS. Possible reasons for this effect are discussed. Copyright 2000 Academic Press.

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Year:  2000        PMID: 10801348     DOI: 10.1006/jmbi.2000.3694

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


  22 in total

1.  Alternative designs for construction of the class II transfer RNA tertiary core.

Authors:  T A Nissan; J J Perona
Journal:  RNA       Date:  2000-11       Impact factor: 4.942

2.  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

3.  Changing identities: tRNA duplication and remolding within animal mitochondrial genomes.

Authors:  Timothy A Rawlings; Timothy M Collins; Rudiger Bieler
Journal:  Proc Natl Acad Sci U S A       Date:  2003-12-12       Impact factor: 11.205

4.  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.

Authors:  Yong-Gang Zheng; Hui Wei; Chen Ling; Franck Martin; Gilbert Eriani; En-Duo Wang
Journal:  Nucleic Acids Res       Date:  2004-06-18       Impact factor: 16.971

5.  A unique insert of leucyl-tRNA synthetase is required for aminoacylation and not amino acid editing.

Authors:  Michael T Vu; Susan A Martinis
Journal:  Biochemistry       Date:  2007-04-04       Impact factor: 3.162

6.  Anticodon-dependent conservation of bacterial tRNA gene sequences.

Authors:  Margaret E Saks; John S Conery
Journal:  RNA       Date:  2007-03-22       Impact factor: 4.942

7.  Isolated CP1 domain of Escherichia coli leucyl-tRNA synthetase is dependent on flanking hinge motifs for amino acid editing activity.

Authors:  Aswini K Betha; Amy M Williams; Susan A Martinis
Journal:  Biochemistry       Date:  2007-05-03       Impact factor: 3.162

8.  Functional segregation of a predicted "hinge" site within the beta-strand linkers of Escherichia coli leucyl-tRNA synthetase.

Authors:  Anjali P Mascarenhas; Susan A Martinis
Journal:  Biochemistry       Date:  2008-03-26       Impact factor: 3.162

9.  Trans-acting RNA inhibits tRNA suppressor activity in vivo.

Authors:  Domenica Gandini Attardi; Glauco P Tocchini-Valentini
Journal:  RNA       Date:  2002-07       Impact factor: 4.942

10.  Mitochondrial genome evolution in fire ants (Hymenoptera: Formicidae).

Authors:  Dietrich Gotzek; Jessica Clarke; DeWayne Shoemaker
Journal:  BMC Evol Biol       Date:  2010-10-07       Impact factor: 3.260

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