The accuracy of translation (CROSBI ID 485351)
Prilog sa skupa u zborniku | sažetak izlaganja sa skupa | domaća recenzija
Podaci o odgovornosti
Weygand-Đurašević, Ivana
engleski
The accuracy of translation
The high level of translational fidelity is ensured by various types of quality control mechanisms, which are adapted to prevent or correct naturally occurring mistakes. Accurate aminoacyl-tRNA synthesis is mostly dependent on the specificity of the aminoacyl-tRNA synthetases, i.e. their ability to choose between competing structurally similar substrates. Our studies have revealed that accurate seryl-tRNA synthesis in yeast and plants is accomplished via tRNA-assisted optimization of amino acid binding to the enzyme active site. Based on our recent kinetic data, a mechanism is proposed by which transient protein:RNA complex activates the cognate amino acid more efficiently and more specifically than the apoenzyme alone. This may proceed via a tRNA-induced conformational change in the enzyme’s active site. As shown by the truncation of tRNA at the 3’-end, terminal adenosine is not important in effecting the rearrangement of the serine binding site. The influence of 3’-truncated tRNASer on the activation of serine by mutated SerRS variants is much less pronounced. These mutants also misactivate structurally similar threonine, indicating that amino acid substitutions in the active site interfere with the ability of the synthetase to discriminate against noncognate substrates. Less significant misactivation of threonine was also observed by wild type SerRS. However, the formation of erroneous threonyl-adenylate is reduced in the presence of tRNASerCC. Thus, the sequence-specific tRNA:SerRS interactions enhance the accuracy of amino acid recognition. Different quality control mechanism in tRNA serylation may be accomplished by the complex formation between SerRS and a nonsynthetase protein. The interaction between yeast SeRS and peroxin Pex21p has been identified in yeast, by using the two-hybrid screen. This was confirmed by an in vitro binding assay with truncated Pex21p fused to glutathione-S-transferase. Experiments revealing potential relevance of this unusual interaction in enhancing the specificity of substrate recognition are in progress.
aminoacyl-tRNA synthetases; accuracy of translation
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Podaci o prilogu
2002.
objavljeno
Podaci o matičnoj publikaciji
Dumić, Jerka
Zagreb: Framaceutsko-biokemijski fakultet
Podaci o skupu
1 st Croatian congress on molecular life sciences with international participation
pozvano predavanje
09.06.2002-13.06.2002
Opatija, Hrvatska