Branlant C, Krol A, Ebel J P
Nucleic Acids Res. 1980 Dec 11;8(23):5567-77. doi: 10.1093/nar/8.23.5567.
The results previously obtained upon studying the L1-23S RNA complex by the fingerprint technique have been reexamined in the light of new data on 23S RNA primary structure. The 23S RNA region that remains associated with the L1 ribosomal protein after RNase digestion of the synthetic complex lies between nucleotides 2067 and 2235 from the 5'-end of the molecule. This region contains a m7G near to the 5'-end and possesses a high degree of mutability in E. coli. Three different sequences were observed in E. coli MRE 600. All three sequences differ in two positions relative to the corresponding sequence in rrnB cistron from E. coli K12. Striking homology is observed between the 23S RNA region associated with protein L1 and the 5'-part of L11 operon. This observation supports the model of feedback regulation of r-proteins synthesis proposed by Yates et al. (PNAS, 77, 1837) and strongly suggests that the region of 23S RNA located between positions 2155 and 2202 is essential for the binding of protein L1.
根据关于23S RNA一级结构的新数据,重新审视了先前通过指纹技术研究L1 - 23S RNA复合物所获得的结果。在对合成复合物进行核糖核酸酶消化后,仍与L1核糖体蛋白结合的23S RNA区域位于分子5'端的核苷酸2067和2235之间。该区域在靠近5'端处含有一个m7G,并且在大肠杆菌中具有高度的变异性。在大肠杆菌MRE 600中观察到三种不同的序列。所有这三种序列相对于来自大肠杆菌K12的rrnB顺反子中的相应序列,在两个位置上有所不同。在与蛋白L1相关的23S RNA区域和L11操纵子的5'部分之间观察到显著的同源性。这一观察结果支持了Yates等人(《美国国家科学院院刊》,77,1837)提出的核糖体蛋白合成反馈调节模型,并强烈表明位于位置2155和2202之间的23S RNA区域对于蛋白L1的结合至关重要。