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This study investigates the effects of the A2058G mutation in 23S rRNA on ribosome behavior in response to varying tryptophan (Trp) concentrations. Through toe-printing techniques, we observed the accumulation of stalled ribosomes in vitro, particularly when Trp was limited in the amino acid mix. Our results demonstrate that ribosomes with the A2058G mutation exhibit reduced sensitivity to Trp, suggesting that this mutation may alter the Trp binding site, influencing translation efficiency and overall protein synthesis.
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U2609C ribosomes Wt A2058G 12.5 50 250 1000 5000 12.5 50 250 1000 5000 12.5 1000 Trp (μM) Trp (μM) 0 100 5000 0 25 100 500 2500 0 25 100 500 2500 C U A G Ribosomes at Trp-12 because of lack of Trp in the AA mix Ribosomes at Trp-12 because of lack of Trp in the AA mix Ribosomes at Pro-24 Ribosomes at Pro-24 Toe-printing, accumulation of stalled ribosomes in vitro
Wild Type A2058G 0 0.2 0.5 1 2 5 10 20 L-Trp(mM) 0 0.2 0.5 1 2 5 10 20 L-Trp(mM) TnaC- tRNAPro TnaC- tRNAPro TnaC TnaC A2058T 0 0.2 0.5 1 2 5 10 20 L-Trp(mM) TnaC- tRNAPro TnaC-tRNAPro accumulation L-Trp(mM) Accumulation of TnaC-tRNAPro in vitro
Beta-Gal expression (MU) 1-M-Trp (mM) Expression of tnaA’-’lacZreporter gene in vivo
Conclusion • The ribosomes containing the A2058G mutant 23S rRNA are less sensitive to Trp. • The change A2058G might affect the Trp binding site.