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The Spliceosome: Design Principles of a Dynamic RNP Machine
Author(s) -
M.C. Wahl,
Cindy L. Will,
Reinhard Lührmann
Publication year - 2009
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2009.02.009
Subject(s) - spliceosome , rna splicing , ribonucleoprotein , biology , intron , small nuclear ribonucleoprotein , microbiology and biotechnology , rna , precursor mrna , rna binding protein , computational biology , genetics , gene
Ribonucleoproteins (RNPs) mediate key cellular functions such as gene expression and its regulation. Whereas most RNP enzymes are stable in composition and harbor preformed active sites, the spliceosome, which removes noncoding introns from precursor messenger RNAs (pre-mRNAs), follows fundamentally different strategies. In order to provide both accuracy to the recognition of reactive splice sites in the pre-mRNA and flexibility to the choice of splice sites during alternative splicing, the spliceosome exhibits exceptional compositional and structural dynamics that are exploited during substrate-dependent complex assembly, catalytic activation, and active site remodeling.

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