Kastelein R A, Berkhout B, Overbeek G P, van Duin J
Gene. 1983 Sep;23(3):245-54. doi: 10.1016/0378-1119(83)90015-x.
The translational efficiency of the coat protein gene of phage MS2 has been examined in vivo with respect to neighbouring sequences. The cloned MS2 DNA has been gradually shortened starting at the 5' or 3' terminus, and its effect on coat protein synthesis monitored. Removal of the 3'-terminal sequences had little influence. In contrast, the gradual removal of the 5'-terminal region profoundly reduces translation. Long before the ribosomal binding site (RBS) of the coat protein (CP) gene is reached, the yield of CP has dropped by one order of magnitude. Functional half-lives of the various messengers were found not to be significantly different. Available evidence indicates that the secondary structure of the RBS in native and shortened MS2 RNA is identical. We infer that important determinants for ribosome recognition lie 5' to the RBS region of the MS2 RNA coat gene.
已在体内研究了噬菌体MS2外壳蛋白基因相对于相邻序列的翻译效率。从5'或3'末端开始逐步缩短克隆的MS2 DNA,并监测其对外壳蛋白合成的影响。去除3'末端序列影响不大。相反,逐步去除5'末端区域会显著降低翻译。早在到达外壳蛋白(CP)基因的核糖体结合位点(RBS)之前,CP的产量就已下降了一个数量级。发现各种信使RNA的功能半衰期没有显著差异。现有证据表明,天然和缩短的MS2 RNA中RBS的二级结构是相同的。我们推断,核糖体识别的重要决定因素位于MS2 RNA外壳基因RBS区域的5'端。