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Molecular architecture of the human Prp19/CDC5L complex.
Grote, Michael; Wolf, Elmar; Will, Cindy L; Lemm, Ira; Agafonov, Dmitry E; Schomburg, Adrian; Fischle, Wolfgang; Urlaub, Henning; Lührmann, Reinhard.
Afiliación
  • Grote M; Department of Cellular Biochemistry, Max Planck Institute for Biophysical Chemistry, Am Fassberg 11, D-37077 Göttingen, Germany.
Mol Cell Biol ; 30(9): 2105-19, 2010 May.
Article en En | MEDLINE | ID: mdl-20176811
Protein complexes containing Prp19 play a central role during catalytic activation of the spliceosome, and Prp19 and its related proteins are major components of the spliceosome's catalytic core RNP. To learn more about the spatial organization of the human Prp19 (hPrp19)/CDC5L complex, which is comprised of hPrp19, CDC5L, PRL1, AD002, SPF27, CTNNBL1, and HSP73, we purified native hPrp19/CDC5L complexes from HeLa cells stably expressing FLAG-tagged AD002 or SPF27. Stoichiometric analyses indicated that, like Saccharomyces cerevisiae NTC (nineteen complex), the human Prp19/CDC5L complex contains four copies of hPrp19. Salt treatment identified a stable core comprised of CDC5L, hPrp19, PRL1, and SPF27. Protein-protein interaction studies revealed that SPF27 directly interacts with each component of the hPrp19/CDC5L complex core and also elucidated several additional, previously unknown interactions between hPrp19/CDC5L complex components. Limited proteolysis of the hPrp19/CDC5L complex revealed a protease-resistant complex comprised of SPF27, the C terminus of CDC5L, and the N termini of PRL1 and hPrp19. Under the electron microscope, purified hPrp19/CDC5L complexes exhibit an elongated, asymmetric shape with a maximum dimension of approximately 20 nm. Our findings not only elucidate the molecular organization of the hPrp19/CDC5L complex but also provide insights into potential protein-protein interactions at the core of the catalytically active spliceosome.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteínas de Unión al ARN / Proteínas de Ciclo Celular / Complejos Multiproteicos Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Mol Cell Biol Año: 2010 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteínas de Unión al ARN / Proteínas de Ciclo Celular / Complejos Multiproteicos Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Mol Cell Biol Año: 2010 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Estados Unidos