Rauhut R, Klug G
Institut für Mikro- und Molekularbiologie der Justus-Liebig-Universität Giessen, Germany.
FEMS Microbiol Rev. 1999 Jun;23(3):353-70. doi: 10.1111/j.1574-6976.1999.tb00404.x.
Messenger RNAs in prokaryotes exhibit short half-lives when compared with eukaryotic mRNAs. Considerable progress has been made during recent years in our understanding of mRNA degradation in bacteria. Two major aspects determine the life span of a messenger in the bacterial cell. On the side of the substrate, the structural features of mRNA have a profound influence on the stability of the molecule. On the other hand, there is the degradative machinery. Progress in the biochemical characterization of proteins involved in mRNA degradation has made clear that RNA degradation is a highly organized cellular process in which several protein components, and not only nucleases, are involved. In Escherichia coli, these proteins are organized in a high molecular mass complex, the degradosome. The key enzyme for initial events in mRNA degradation and for the assembly of the degradosome is endoribonuclease E. We discuss the identified components of the degradosome and its mode of action. Since research in mRNA degradation suffers from dominance of E. coli-related observations we also look to other organisms to ask whether they could possibly follow the E. coli standard model.
与真核生物的信使核糖核酸(mRNA)相比,原核生物中的mRNA半衰期较短。近年来,我们对细菌中mRNA降解的理解取得了相当大的进展。有两个主要方面决定了细菌细胞中信使的寿命。在底物方面,mRNA的结构特征对分子的稳定性有深远影响。另一方面,存在降解机制。参与mRNA降解的蛋白质的生化特性研究进展表明,RNA降解是一个高度组织化的细胞过程,其中涉及多种蛋白质成分,而不仅仅是核酸酶。在大肠杆菌中,这些蛋白质组装成一个高分子量复合物——降解体。mRNA降解起始事件和降解体组装的关键酶是核糖核酸内切酶E。我们讨论了已确定的降解体成分及其作用方式。由于mRNA降解的研究主要基于与大肠杆菌相关的观察结果,我们也关注其他生物,以探讨它们是否可能遵循大肠杆菌的标准模式。