Berkhout B, Kastelein R A, van Duin J
Gene. 1985;37(1-3):171-9. doi: 10.1016/0378-1119(85)90270-7.
In overlapping reading frames of prokaryotic mRNA, the ribosome-binding site (RBS) of the downstream cistron is part of the coding sequence of the upstream message. We have examined whether the rate of translation in Escherichia coli can be sufficiently high to preclude the use of an RBS in initiation of protein synthesis when it is part of an actively decoded reading frame. The two sets of gene overlap present in the RNA phage MS2 are used as a model system. We find that translation of an upstream cistron can fully block initiation of protein synthesis at the overlapping RBS of the downstream cistron. Nonsense mutations in the upstream gene restore the translation of the downstream gene.
在原核生物信使核糖核酸(mRNA)的重叠阅读框中,下游顺反子的核糖体结合位点(RBS)是上游信息编码序列的一部分。我们研究了在大肠杆菌中,当核糖体结合位点是一个正在被积极解码的阅读框的一部分时,其翻译速率是否能够足够高,从而排除在蛋白质合成起始过程中对核糖体结合位点的使用。RNA噬菌体MS2中存在的两组基因重叠被用作一个模型系统。我们发现,上游顺反子的翻译能够完全阻断下游顺反子重叠核糖体结合位点处的蛋白质合成起始。上游基因中的无义突变可恢复下游基因的翻译。