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  A genome-scale RNAi screen for Oct4 modulators defines a role of the Paf1 complex for embryonic stem cell identity

Ding, L., Paszkowski-Rogacz, M., Nitzsche, A., Slabicki, M. M., Heninger, A.-K., Vries, I. d., et al. (2009). A genome-scale RNAi screen for Oct4 modulators defines a role of the Paf1 complex for embryonic stem cell identity. Cell Stem Cell, 4(5), 403-415.

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Ding, Li1, Autor           
Paszkowski-Rogacz, Maciej1, Autor           
Nitzsche, Anja1, Autor           
Slabicki, Mikolaj Michal1, Autor           
Heninger, Anne-Kristin1, Autor           
Vries, Ingrid de, Autor
Kittler, Ralf1, Autor           
Junqueira, Magno1, Autor           
Shevchenko, Andrej1, Autor           
Schulz, Herbert, Autor
Hubner, Norbert, Autor
Doss, Michael Xavier, Autor
Sachinidis, Agapios, Autor
Hescheler, Juergen, Autor
Iacone, Roberto, Autor
Anastassiadis, Konstantinos2, Autor
Stewart, A Francis, Autor
Pisabarro, M Teresa, Autor
Caldarelli, Antonio1, Autor           
Poser, Ina1, Autor           
Theis, Mirko1, Autor           Buchholz, Frank1, Autor            mehr..
Affiliations:
1Max Planck Institute of Molecular Cell Biology and Genetics, Max Planck Society, ou_2340692              
2Max Planck Society, ou_persistent13              

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 Zusammenfassung: Pluripotent embryonic stem cells (ESCs) maintain self-renewal while ensuring a rapid response to differentiation cues. The identification of genes maintaining ESC identity is important to develop these cells for their potential therapeutic use. Here we report a genome-scale RNAi screen for a global survey of genes affecting ESC identity via alteration of Oct4 expression. Factors with the strongest effect on Oct4 expression included components of the Paf1 complex, a protein complex associated with RNA polymerase II. Using a combination of proteomics, expression profiling, and chromatin immunoprecipitation, we demonstrate that the Paf1C binds to promoters of key pluripotency genes, where it is required to maintain a transcriptionally active chromatin structure. The Paf1C is developmentally regulated and blocks ESC differentiation upon overexpression, and the knockdown in ESCs causes expression changes similar to Oct4 or Nanog depletions. We propose that the Paf1C plays an important role in maintaining ESC identity.

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 Datum: 2009
 Publikationsstatus: Erschienen
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 Identifikatoren: eDoc: 463155
Anderer: 1230
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Titel: Cell Stem Cell
Genre der Quelle: Zeitschrift
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Ort, Verlag, Ausgabe: -
Seiten: - Band / Heft: 4 (5) Artikelnummer: - Start- / Endseite: 403 - 415 Identifikator: -