Bläsi U, Nam K, Lubitz W, Young R
Department of Biochemistry and Biophysics, Texas A&M University, College Station 77843.
J Bacteriol. 1990 Oct;172(10):5617-23. doi: 10.1128/jb.172.10.5617-5623.1990.
The lysis gene E of bacteriophage phi X174 is entirely embedded in gene D. Expression studies of genes D and E in Escherichia coli minicells and lysis times obtained in the presence or absence of D translation showed that the simultaneous expression of gene D does not affect protein E production. Thus, unlike other overlapping gene pairs, gene E expression is independent from the upstream translation of gene D. lacZ fusion studies and primer extension inhibition analysis (toeprinting) revealed an intrinsically weak E ribosome-binding site, which seems to be the major factor determining the low expression rate of the gene and thus proper scheduling of cell lysis.
噬菌体φX174的裂解基因E完全嵌入在基因D中。在大肠杆菌微小细胞中对基因D和E进行表达研究,并在有或没有D翻译的情况下测定裂解时间,结果表明基因D的同时表达不影响蛋白质E的产生。因此,与其他重叠基因对不同,基因E的表达独立于基因D的上游翻译。lacZ融合研究和引物延伸抑制分析(足迹法)揭示了一个本质上较弱的E核糖体结合位点,这似乎是决定该基因低表达率并因此决定细胞裂解适当时间安排的主要因素。