Noller H F
Center for Molecular Biology of RNA, Department of Molecular, Cell and Developmental Biology, Sinsheimer Laboratories, University of California, Santa Cruz, Santa Cruz, CA 95064, USA.
Biochimie. 2006 Aug;88(8):935-41. doi: 10.1016/j.biochi.2006.04.006. Epub 2006 Apr 27.
Prior to the emergence of crystal structures of the ribosome, different ribosomal functions were identified with specific regions of ribosomal RNA by biochemical and genetic approaches. In particular, three universally conserved bases of 16S rRNA, G530, A1492 and A1493, were implicated in the interaction of the incoming aminoacyl-tRNA with the 30S subunit and mRNA. The conserved region surrounding A1492 and A1493 was called the "decoding site", based on the results of chemical probing experiments and antibiotic resistance mutations. Crystallographic studies from the Ramakrishnan laboratory have now shown that G530 loop, A1492 and A1493 undergo localized conformational changes to form an RNA structure that positions these three bases to inspect the accuracy of the codon-anticodon match with high stereochemical precision, using A-minor interactions. Some results from the pre-X-ray era may provide clues to further aspects of the decoding process.
在核糖体晶体结构出现之前,通过生化和遗传学方法,不同的核糖体功能与核糖体RNA的特定区域相关联。特别是,16S rRNA的三个普遍保守碱基G530、A1492和A1493与进入的氨酰tRNA与30S亚基和mRNA的相互作用有关。基于化学探测实验和抗生素抗性突变的结果,围绕A1492和A1493的保守区域被称为“解码位点”。Ramakrishnan实验室的晶体学研究现已表明,G530环、A1492和A1493会发生局部构象变化,形成一种RNA结构,该结构利用A- minor相互作用将这三个碱基定位,以高立体化学精度检查密码子-反密码子匹配的准确性。X射线时代之前的一些结果可能为解码过程的其他方面提供线索。