Structural Insights into Nuclear p e-mRNA Splicing in Higher Eukaryotes

被引:158
作者
Kastner, Berthold [1 ]
Will, Cindy L. [1 ]
Stark, Holger [2 ]
Luehrmann, Reinhard [1 ]
机构
[1] Max Planck Inst Biophys Chem, Dept Cellular Biochem, D-37077 Gottingen, Germany
[2] Max Planck Inst Biophys Chem, Dept Struct Dynam, D-37077 Gottingen, Germany
关键词
U4/U6.U5; TRI-SNRNP; HUMAN SPLICEOSOME; MOLECULAR ARCHITECTURE; ACTIVATED SPLICEOSOME; MECHANISTIC INSIGHTS; PROTEOMIC ANALYSIS; BRANCH SITE; U2; SNRNP; STEP; PROTEIN;
D O I
10.1101/cshperspect.a032417
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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.
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页数:20
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