Gregory S T, Dahlberg A E
Section of Biochemistry, Brown University, Providence, RI 02912.
FEBS Lett. 1995 Mar 13;361(1):25-8. doi: 10.1016/0014-5793(95)00132-s.
Mutations in the anticodon of tRNA(Glu) (UUC) were isolated or constructed and characterized for their ability to suppress cognate nonsense or missense mutations in vivo. The C36-to-A36 transversion mutation was isolated as an ochre and an amber suppressor, while the G36 transversion was selected as a CAG missense suppressor. tRNA(Glu) suppressors of an AAG missense mutation could not be isolated, and a U36 transition mutation introduced into tRNA(Glu) in vitro conferred no suppressor phenotype. Over-expression of glutamyl-tRNA synthetase did not increase the activity of the U36 mutant tRNA(Glu), suggesting a defect at the level of translation rather than at the level of synthetase recognition.
分离或构建了tRNA(Glu)(UUC)反密码子中的突变,并对其在体内抑制同源无义或错义突变的能力进行了表征。C36到A36的颠换突变被分离为赭石型和琥珀型抑制子,而G36颠换被选为CAG错义抑制子。无法分离出AAG错义突变的tRNA(Glu)抑制子,体外引入tRNA(Glu)的U36转换突变没有赋予抑制子表型。谷氨酰胺-tRNA合成酶的过表达并没有增加U36突变体tRNA(Glu)的活性,这表明是翻译水平而非合成酶识别水平存在缺陷。