Department of Cellular Biochemistry, Max Planck Institute for Biophysical Chemistry, D-37077 Göttingen, Germany.
Department of Structural Dynamics, Max Planck Institute for Biophysical Chemistry, D-37077 Göttingen, Germany.
Cold Spring Harb Perspect Biol. 2019 Nov 1;11(11):a032417. doi: 10.1101/cshperspect.a032417.
The spliceosome is a highly complex, dynamic ribonucleoprotein molecular machine that undergoes numerous structural and compositional rearrangements that lead to the formation of its active site. Recent advances in cyroelectron microscopy (cryo-EM) have provided a plethora of near-atomic structural information about the inner workings of the spliceosome. Aided by previous biochemical, structural, and functional studies, cryo-EM has confirmed or provided a structural basis for most of the prevailing models of spliceosome function, but at the same time allowed novel insights into splicing catalysis and the intriguing dynamics of the spliceosome. The mechanism of pre-mRNA splicing is highly conserved between humans and yeast, but the compositional dynamics and ribonucleoprotein (RNP) remodeling of the human spliceosome are more complex. Here, we summarize recent advances in our understanding of the molecular architecture of the human spliceosome, highlighting differences between the human and yeast splicing machineries.
剪接体是一种高度复杂、动态的核糖核蛋白分子机器,经历了许多结构和组成上的重排,从而形成其活性部位。最近的冷冻电子显微镜(cryo-EM)技术进步提供了大量关于剪接体内部运作的近原子结构信息。在之前的生化、结构和功能研究的辅助下,cryo-EM 已经证实或为大多数流行的剪接体功能模型提供了结构基础,但同时也为剪接催化和剪接体的有趣动力学提供了新的见解。人类和酵母之间的前 mRNA 剪接机制高度保守,但人类剪接体的组成动力学和核糖核蛋白(RNP)重塑更为复杂。在这里,我们总结了我们对人类剪接体分子结构的理解的最新进展,强调了人类和酵母剪接机制之间的差异。