Drabkin H J, Park H J, RajBhandary U L
Department of Biology, Massachusetts Institute of Technology, Cambridge 02139, USA.
Mol Cell Biol. 1996 Mar;16(3):907-13. doi: 10.1128/MCB.16.3.907.
As an approach to inducible suppression of nonsense mutations in mammalian and in higher eukaryotic cells, we have analyzed the expression of an Escherichia coli glutamine-inserting amber suppressor tRNA gene in COS-1 and CV-1 monkey kidney cells. The tRNA gene used has the suppressor tRNA coding sequence flanked by sequences derived from a human initiator methionine tRNA gene and has two changes in the coding sequence. This tRNA gene is transcribed, and the transcript is processed to yield the mature tRNA in COS-1 and CV-1 cells. We show that the tRNA is not aminoacylated in COS-1 cells by any of the endogenous aminoacyl-tRNA synthetases and is therefore not functional as a suppressor. Concomitant expression of the E. coli glutaminyl-tRNA synthetase gene results in aminoacylation of the suppressor tRNA and its functioning as a suppressor. These results open up the possibility of attempts at regulated suppression of nonsense codons in mammalian cells by regulating expression of the E. coli glutaminyl-tRNA synthetase gene in an inducible, cell-type specific, or developmentally regulated manner.
作为一种诱导抑制哺乳动物和高等真核细胞中无义突变的方法,我们分析了大肠杆菌谷氨酰胺插入琥珀抑制tRNA基因在COS-1和CV-1猴肾细胞中的表达。所使用的tRNA基因的抑制tRNA编码序列两侧是源自人起始甲硫氨酸tRNA基因的序列,并且编码序列中有两个变化。该tRNA基因在COS-1和CV-1细胞中转录,转录本经加工产生成熟tRNA。我们发现该tRNA在COS-1细胞中未被任何内源性氨酰tRNA合成酶氨酰化,因此不能作为抑制子发挥作用。同时表达大肠杆菌谷氨酰胺tRNA合成酶基因会导致抑制tRNA氨酰化并使其作为抑制子发挥作用。这些结果为通过以诱导型、细胞类型特异性或发育调控方式调节大肠杆菌谷氨酰胺tRNA合成酶基因的表达来尝试在哺乳动物细胞中调控抑制无义密码子开辟了可能性。