The modified wobble nucleoside uridine-5-oxyacetic acid in tRNA cmo5UGGPro promotes reading of all four proline codons in vivo

Abstract

In Salmonella enterica serovar Typhimurium five of the eight family codon boxes are decoded by a tRNA having the modified nucleoside uridine-5-oxyacetic acid (cmo5U) as a wobble nucleoside present in position 34 of the tRNA. In the proline family codon box, one (tRNAcmo5UGGPro) of the three tRNAs that reads the four proline codons has cmo5U34. According to theoretical predictions and several results obtained in vitro, cmo5U34 should base pair with A, G, and U in the third position of the codon but not with C. To analyze the function of cmo 5U34 in tRNAcmo5UGGPro in vivo, we first identified two genes (cmoA and, cmoB) involved in the synthesis of cmo 5U34. The null mutation cmoB2 results in tRNA having 5-hydroxyuridine (ho5U34) instead of cmo5U34, whereas the null mutation cmoA1 results in the accumulation of 5-methoxyuridine (mo5U34) and ho5U34 in tRNA. The results suggest that the synthesis of cmo 5U34 occurs as follows: U34 →? ho5U →CmoB mo5U →CmoA? cmo5U. We introduced the cmoA1 or the cmoB2 null mutations into a strain that only had tRNAcmo5UGGPro and thus lacked the other two proline-specific tRNAs normally present in the cell. From analysis of growth rates of various strains and of the frequency of +1 frameshifting at a CCC-U site we conclude: (1) unexpectedly, tRNAcmo5UGGPro is able to read all four proline codons; (2) the presence of ho5U34 instead of cmo5U34 in this tRNA reduces the efficiency with which it reads all four codons; and (3) the fully modified nucleoside is especially important for reading proline codons ending with U or C.