Oakes M I, Kahan L, Lake J A
Molecular Biology Institute, University of California, Los Angeles 90024.
J Mol Biol. 1990 Feb 20;211(4):907-18. doi: 10.1016/0022-2836(90)90083-X.
Seven regions of 16 S rRNA have been located on the surface of the 30 S ribosomal subunit by DNA-hybridization electron microscopy. This information has been incorporated into a model for the tertiary structure of 16 S rRNA, accounting for approximately 40% of the total 16 S rRNA. A structure labeled the platform ring is proposed for a region of rRNA within the central domain. This structure rings the edges of the platform and includes regions 655-751 and 769-810. Another region, the recognition complex, consists of nucleotides 500 to 545, and occupies a region on the exterior surface of the subunit near the elongation factor Tu binding site. Ribosomal proteins that have been mapped by immunoelectron microscopy are superimposed onto the model in order to examine possible regions of interaction. Good correlation between the model locations of ribosomal proteins, and regions of rRNA protected by ribosomal proteins provide independent support for this model.
通过DNA杂交电子显微镜已将16 S rRNA的七个区域定位在30 S核糖体亚基的表面。该信息已被纳入16 S rRNA三级结构模型,约占16 S rRNA总量的40%。针对中央结构域内rRNA的一个区域提出了一种标记为平台环的结构。该结构环绕平台边缘,包括655 - 751区域和769 - 810区域。另一个区域,识别复合体,由500至545位核苷酸组成,占据亚基外表面靠近延伸因子Tu结合位点的一个区域。已通过免疫电子显微镜定位的核糖体蛋白被叠加到该模型上,以检查可能的相互作用区域。核糖体蛋白的模型位置与受核糖体蛋白保护的rRNA区域之间的良好相关性为该模型提供了独立支持。