Eichler D C, Craig N
Department of Biochemistry & Molecular Biology, University of South Florida College of Medicine, Tampa 33612.
Prog Nucleic Acid Res Mol Biol. 1994;49:197-239. doi: 10.1016/s0079-6603(08)60051-3.
In summary, it can be argued that the understanding of eukaryotic rRNA processing is no less important than the understanding of mRNA maturation, since the capacity of a cell to carry out protein synthesis is controlled, in part, by the abundance of ribosomes. Processing of pre-rRNA is highly regulated, involving many cellular components acting either alone or as part of a complex. Some of these components are directly involved in the modification and cleavage of the precursor rRNA, while others direct the packaging of the rRNA into ribosome subunits. As is the case for pre-mRNA processing, snoRNPs are clearly involved in eukaryotic rRNA processing, and have been proposed to assemble with other proteins into at least one complex called a "processosome" (17), which carries out the ordered processing of the pre-rRNA and its assembly into ribosomes. The formation of a processing complex clearly makes possible the regulation required to coordinate the abundance of ribosomes with the physiological and developmental changes of a cell. It may be that eukaryotic rRNA processing is even more complex than pre-mRNA maturation, since pre-rRNA undergoes extensive nucleotide modification and is assembled into a complex structure called the ribosome. Undoubtedly, features of the eukaryotic rRNA-processing pathway have been conserved evolutionarily, and the genetic approach available in yeast research (6) should provide considerable knowledge that will be useful for other investigators working with higher eukaryotic systems. Interestingly, it was originally hoped that the extensive work and understanding of bacterial ribosome formation would provide a useful paradigm for the process in eukaryotes. However, although general features of ribosome structure and function are highly conserved between bacterial and eukaryotic systems, the basic strategy in ribosome biogenesis seems to be, for the most part, distinctly different. Thus, the detailed molecular mechanisms for rRNA processing in each kingdom will have to be independently deciphered in order to elucidate the features and regulation of this important process for cell survival.
总之,可以说对真核生物rRNA加工的理解与对mRNA成熟的理解同样重要,因为细胞进行蛋白质合成的能力部分受核糖体丰度的控制。前体rRNA的加工受到高度调控,涉及许多单独起作用或作为复合物一部分起作用的细胞成分。其中一些成分直接参与前体rRNA的修饰和切割,而其他成分则指导rRNA包装到核糖体亚基中。与前体mRNA加工的情况一样,snoRNP显然参与真核生物rRNA加工,并已被提议与其他蛋白质组装成至少一种称为“加工体”的复合物(17),该复合物对前体rRNA进行有序加工并将其组装成核糖体。加工复合物的形成显然使得协调核糖体丰度与细胞生理和发育变化所需的调控成为可能。真核生物rRNA加工可能甚至比前体mRNA成熟更复杂,因为前体rRNA经历广泛的核苷酸修饰并组装成称为核糖体的复杂结构。毫无疑问,真核生物rRNA加工途径的特征在进化上是保守的,酵母研究中可用的遗传学方法(6)应该会提供大量知识,这将对研究高等真核生物系统的其他研究人员有用。有趣的是,最初人们希望对细菌核糖体形成的广泛研究和理解能为真核生物中的这一过程提供有用的范例。然而,尽管细菌和真核生物系统之间核糖体结构和功能的一般特征高度保守,但核糖体生物发生的基本策略在很大程度上似乎明显不同。因此,为了阐明这一细胞存活重要过程的特征和调控,每个王国中rRNA加工的详细分子机制都必须独立破译。