Afasozjev R D
Mol Biol (Mosk). 1995 Jan-Feb;29(1):91-6.
The stability of phosphodiester bonds in tRNA(Trp) (E. coli, bovine) and tRNA(Phe) (yeast) synthesized in vitro was studied in the complexes with cognate aminoacyl-tRNA synthetases. In contrast to E. coli tRNA(Gln) where synthetase-induced cleavage has been reported, we have failed to observe this effect with tRNA(Trp) and tRNA(Phe). Consequently, the weakness of sugar-phosphate backbone of tRNA-transcripts in the complexes is not a common feature for all tRNA-synthetase pairs. The cleavage mechanism in the case of tRNA(Gln) remains obscure.
研究了体外合成的tRNA(Trp)(大肠杆菌、牛)和tRNA(Phe)(酵母)与同源氨酰-tRNA合成酶形成的复合物中磷酸二酯键的稳定性。与已报道有合成酶诱导切割现象的大肠杆菌tRNA(Gln)不同,我们在tRNA(Trp)和tRNA(Phe)中未观察到这种效应。因此,复合物中tRNA转录本糖磷酸骨架的脆弱性并非所有tRNA-合成酶对的共同特征。tRNA(Gln)的切割机制仍不清楚。