Institute for Cell and Molecular Biosciences (ICaMB), Newcastle University, Newcastle upon Tyne, UK.
Trends Biochem Sci. 2013 Oct;38(10):485-93. doi: 10.1016/j.tibs.2013.06.013. Epub 2013 Aug 2.
In eukaryotes, the exosome complex degrades RNA backbones and plays key roles in RNA processing and surveillance. It was predicted that RNA substrates are threaded through a central channel. This pathway is conserved between eukaryotic and archaeal complexes, even though nuclease activity was lost from the nine-subunit eukaryotic core (EXO-9) and transferred to associated proteins. The exosome cooperates with nuclear and cytoplasmic cofactors, including RNA helicases Mtr4 and Ski2, respectively. Structures of an RNA-bound exosome and both helicases revealed how substrates are channeled through EXO-9 to the associated nuclease Rrp44. Recent high-throughput analyses provided fresh insights relating exosome structure to its diverse in vivo functions. They also revealed surprisingly high degradation rates for newly synthesized RNAs, particularly RNA polymerase III transcripts.
在真核生物中,核酶体复合物降解 RNA 骨架,并在 RNA 加工和监控中发挥关键作用。据预测,RNA 底物穿过中央通道。这条途径在真核生物和古菌复合物之间是保守的,尽管核酶活性已经从九亚基的真核核心(EXO-9)中丢失,并转移到相关的蛋白上。核酶体与核和细胞质辅助因子合作,包括 RNA 解旋酶 Mtr4 和 Ski2。RNA 结合核酶体和两种解旋酶的结构揭示了底物如何通过 EXO-9 被转运到相关的核酶 Rrp44。最近的高通量分析提供了关于核酶体结构与其多种体内功能的新见解。它们还揭示了新合成的 RNA,特别是 RNA 聚合酶 III 转录物的降解率非常高。