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tRNA structure and ribosomal function I ... s enhance first position wobble


tRNA structure and ribosomal function. I. tRNA nucleotide 27-43 mutations enhance first position wobble.

47

Transfer RNA su7 G36 is a derivative of tRNA(Trp) with a 3'GUC anticodon complementary to the glutamine codon CAG. This tRNA requires a normally forbidden G-U wobble at the first codon position to suppress a UAG (amber) termination codon. Measurement of amber suppression by mutated su7 G36 tRNAs and correction for tRNA levels and aminoacylation allowed calculation of KUAG, a linearized index of in vivo ribosomal function. Following saturating mutagenesis of the anticodon arm of su7 G36, screening for UAG suppression using a lacZ reporter yielded tRNAs with up to 40-fold increased first position G-U wobble, judged from KUAG. The parental anticodon helix has minimized this type of miscoding, and virtually all changes in the top base-pair of the anticodon helix, nucleotides (nt) 27-43, increased the error. Thus, misincorporation of amino acids due to aberrant first position wobble is apparently prevented by normal tRNA structure, which is specifically altered by substitution at nt 27-43, the top base-pair of the anticodon helix. All 16 permutations of nt 27-43, the hotspot for increased wobble, were subsequently constructed and compared. Comparison of values for tRNA coding function, tRNA level, and aminoacylation for the 16 suggest that a tRNA conformational change, specifically involving both nt 27-43, differentially affects all these tRNA functions. This conformational alteration, which presumably occurs normally on the ribosome, appears more complex than simple breakage of the normal 27-43 base-pair. We suggest that the change is in the angle and/or flexibility of the tRNA L-shape. Among these 16 tRNAs, efficient wobble is strongly and inversely correlated with good aminoacylation and high tRNA levels; this quality may have been selected. Constraints on the sequences of natural tRNAs suggest that nt 27-43 have effects on function in many tRNAs.


Schultz DW, Yarus M

Journal of molecular biology

1994-02-04 00:00

235

5

1381-94

Anticodon,Base Composition,Base Sequence,Cloning, Molecular,Codon,Escherichia coli,Genes, Bacterial,Glutamine,Models, Structural,Molecular Sequence Data,Mutagenesis,Nucleic Acid Conformation,RNA, Transfer,RNA, Transfer, Trp,Regression Analysis,Anticodon,Codon,RNA, Transfer, Trp,Glutamine,RNA, Transfer

Department of Molecular, Cellular, and Developmental Biology, University of Colorado, Boulder 80309-0347

J. Mol. Biol.

NIGMS GM30881

0022-2836

10.1006/jmbi.1994.1095

S0022-2836(84)71095-3

1502

True

8107080

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