Abstract
The splicing process, which removes intervening sequences from messenger RNA (mRNA) precursors is essential to gene expression in eukaryotic cells. This site-specific process requires precise sequence recognition at the boundaries of an intervening sequence, but the mechanism of this recognition is not understood. The splicing of mRNA precursors occurs in a multicomponent complex termed the spliceosome. Such an assembly of components is likely to play a key role in specifying those sequences to be spliced. In order to analyze spliceosome structure, a stringent approach was developed to obtain splicing complexes free of cellular contaminants. This approach is a form of affinity chromatography based on the high specificity of the biotin-streptavidin interaction. A minimum of three subunits: U2, U5, and U4 + U6 small nuclear ribonucleoprotein particles were identified in the 35 S spliceosome structure, which also contains the bipartite RNA intermediate of splicing. A 25 S presplicing complex contained only the U2 particle. The multiple subunit structure of the spliceosome has implications for the regulation of a splicing event and for its possible catalysis by ribozyme or ribozymes.
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Dates
Type | When |
---|---|
Created | 18 years, 10 months ago (Oct. 5, 2006, 4:28 p.m.) |
Deposited | 1 year, 7 months ago (Jan. 14, 2024, 4:46 a.m.) |
Indexed | 11 months, 4 weeks ago (Sept. 3, 2024, 11:46 a.m.) |
Issued | 38 years, 11 months ago (Sept. 19, 1986) |
Published | 38 years, 11 months ago (Sept. 19, 1986) |
Published Print | 38 years, 11 months ago (Sept. 19, 1986) |
@article{Grabowski_1986, title={Affinity Chromatography of Splicing Complexes: U2, U5, and U4 + U6 Small Nuclear Ribonucleoprotein Particles in the Spliceosome}, volume={233}, ISSN={1095-9203}, url={http://dx.doi.org/10.1126/science.3638792}, DOI={10.1126/science.3638792}, number={4770}, journal={Science}, publisher={American Association for the Advancement of Science (AAAS)}, author={Grabowski, Paula J. and Sharp, Phillip A.}, year={1986}, month=sep, pages={1294–1299} }