Gregory S T, Lieberman K R, Dahlberg A E
Section of Biochemistry, Brown University, Providence, RI 02912.
Nucleic Acids Res. 1994 Feb 11;22(3):279-84. doi: 10.1093/nar/22.3.279.
We have produced mutations in a cloned Escherichia coli 23S rRNA gene at positions G2252 and G2253. These sites are protected in chemical footprinting studies by the 3' terminal CCA of P site-bound tRNA. Three possible base changes were introduced at each position and the mutations produced a range of effects on growth rate and translational accuracy. Growth of cells bearing mutations at 2252 was severely compromised while the only mutation at 2253 causing a marked reduction in growth rate was a G to C transversion. Most of the mutations affected translational accuracy, causing increased readthrough of UGA, UAG and UAA nonsense mutations as well as +1 and -1 frameshifting in a lacZ reporter gene in vivo. C2253 was shown to act as a suppressor of a UGA nonsense mutation at codon 243 of the trpA gene. The C2253 mutation was also found not to interact with alleles of rpsL coding for restrictive forms of ribosomal protein S12. These results provide further evidence that nucleotides localized to the P site in the 50S ribosomal subunit influence the accuracy of decoding in the ribosomal A site.
我们在克隆的大肠杆菌23S rRNA基因的G2252和G2253位点产生了突变。在化学足迹研究中,这些位点受到P位点结合的tRNA的3'末端CCA的保护。在每个位点引入了三种可能的碱基变化,这些突变对生长速率和翻译准确性产生了一系列影响。携带2252位点突变的细胞生长严重受损,而2253位点唯一导致生长速率显著降低的突变是G到C的颠换。大多数突变影响翻译准确性,导致体内UGA、UAG和UAA无义突变的通读增加,以及lacZ报告基因中的+1和-1移码。C2253被证明可作为trpA基因第243密码子处UGA无义突变的抑制子。还发现C2253突变与编码核糖体蛋白S12限制性形式的rpsL等位基因不相互作用。这些结果进一步证明,定位于50S核糖体亚基P位点的核苷酸会影响核糖体A位点的解码准确性。