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Functional and chromatin analyses of embryonic stem cell pluripotency by reversible knockdown of bivalent domain regulators

Antragsteller Professor Dr. Albrecht M. Müller (†)
Fachliche Zuordnung Zellbiologie
Förderung Förderung von 2008 bis 2014
Projektkennung Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 66352807
 
Erstellungsjahr 2014

Zusammenfassung der Projektergebnisse

The aim of this work was to study Pcgf6 function in pluripotent cells. We observed that Pcgf6 in contrast to its paralogs was abundantly expressed in undifferentiated ESCs, blastocysts and in testes. Further, we show that in comparison to ESCs cultured under standard conditions, Pcgf6 expression is higher in ESCs cultured in 2i medium and lower in EpiSCs. Upon ESC differentiation, Pcgf6 expression declined. The consequences of Pcgf6 KD in ESCs included reduced colony formation, increased expression of differentiation-associated genes, including mesodermal genes, and increased in vitro ESC hemangioblast-type and hematopoietic differentiation outcomes. Pcgf6, when over-expressed in MEFs together with Oct4, Klf4 and c-Myc, was able to replace Sox2 in the generation of germline-competent iPS cells. OSKM reprogramming of MEFs under Pcgf6 KD resulted in reduced iPS colony numbers. These analyses indicate that Pcgf6 is non-redundantly involved in maintaining the pluripotent nature of ESCs and functions in iPS reprogramming. In summary, we are just beginning to elucidate the role of PRC1 variants in ESC biology and more detailed analyses are required to better understand the relevance of this fascinating and highly elaborate group of chromatin regulators for the pluripotent state. The data shown here are basis for a planned grant application analyzing molecular functions and interaction partners of Pcgf6 in ESCs.

Projektbezogene Publikationen (Auswahl)

 
 

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