Yates J L, Nomura M
Cell. 1980 Sep;21(2):517-22. doi: 10.1016/0092-8674(80)90489-4.
We studied the synthesis of ribosomal proteins encoded by the S10 operon, an eleven gene operon from the str-spc region of the E. coli chromosome, using a lambda fus3 DNA-directed, in vitro protein synthesizing system. Addition of ribosomal protein L4 (1 microM) to in vitro protein synthesis reactions caused selective inhibition of synthesis of the promoter-proximal proteins of the S10 operon, S10, L3, L4, L23 and possibly L2. Proteins of the S10 operon other than L4 did not cause selective inhibition of protein synthesis. Autoregulatory ribosomal proteins previously identified from other operons, L1, S4 and S8, did not inhibit protein synthesis from the S10 operon; nor did L4 cause significant inhibition of protein synthesis from operons other than the S10 operon. As with L1, S4 and S8, L4 inhibits gene expression at the level of translation.
我们使用λfus3 DNA 指导的体外蛋白质合成系统,研究了由 S10 操纵子编码的核糖体蛋白的合成,S10 操纵子是来自大肠杆菌染色体 str-spc 区域的一个包含 11 个基因的操纵子。向体外蛋白质合成反应中添加核糖体蛋白 L4(1μM)会导致对 S10 操纵子中启动子近端蛋白 S10、L3、L4、L23 以及可能的 L2 的合成产生选择性抑制。除 L4 外,S10 操纵子的蛋白质不会导致蛋白质合成的选择性抑制。先前从其他操纵子中鉴定出的自调节核糖体蛋白 L1、S4 和 S8 不会抑制 S10 操纵子的蛋白质合成;L4 也不会对 S10 操纵子以外的操纵子的蛋白质合成产生显著抑制。与 L1、S4 和 S8 一样,L4 在翻译水平上抑制基因表达。