Hartung Sophia, Hopfner Karl-Peter
Center for Integrated Protein Science and Gene Center, Department of Chemistry and Biochemistry, Ludwig-Maximilians-University Munich, Feodor-Lynen-Strasse 25, 81377 Munich, Germany.
Biochem Soc Trans. 2009 Feb;37(Pt 1):83-7. doi: 10.1042/BST0370083.
The RNA exosome is a multisubunit exonuclease involved in numerous RNA maturation and degradation processes. Exosomes are found in eukaryotes and archaea and are related to bacterial polynucleotide phosphorylates. Over the past years structural and biochemical analysis revealed that archaeal exosomes have a large processing chamber with three phosphorolytic active sites that degrade RNA in the 3'-->5' direction in a highly processive manner. A narrow entry pore, framed by putative RNA-binding domains, could account for the high processivity and also prevent degradation of structured RNA. The phosphorolytic nuclease activity is reversible, leading to formation of heteropolymeric tails from nucleoside diphosphates as substrate. This reversibility is difficult to regulate, suggesting why, during evolution and emergence of stable poly(A) tails in eukaryotes, polyadenylation and nuclease activities in the human exosome and associated factors have been separated.
RNA外切体是一种多亚基核酸外切酶,参与众多RNA成熟和降解过程。外切体存在于真核生物和古细菌中,与细菌多核苷酸磷酸化酶相关。在过去几年中,结构和生化分析表明,古细菌外切体有一个大的加工腔,带有三个磷酸解活性位点,以高度连续的方式沿3'→5'方向降解RNA。一个由假定的RNA结合结构域构成的狭窄入口孔,可以解释其高连续性,也能防止结构化RNA的降解。磷酸解核酸酶活性是可逆的,导致以核苷二磷酸为底物形成杂聚尾巴。这种可逆性难以调控,这就解释了为什么在真核生物中稳定聚腺苷酸尾巴的进化和出现过程中,人类外切体中的多聚腺苷酸化和核酸酶活性以及相关因子已经分离。