| Autor: |
Daniel G; Guillaume Daniel, Udo Schmidt-Edelkraut, Dietmar Spengler, Anke Hoffmann, Max Planck Institute of Psychiatry, Translational Research, 80804 Munich, Germany., Schmidt-Edelkraut U; Guillaume Daniel, Udo Schmidt-Edelkraut, Dietmar Spengler, Anke Hoffmann, Max Planck Institute of Psychiatry, Translational Research, 80804 Munich, Germany., Spengler D; Guillaume Daniel, Udo Schmidt-Edelkraut, Dietmar Spengler, Anke Hoffmann, Max Planck Institute of Psychiatry, Translational Research, 80804 Munich, Germany., Hoffmann A; Guillaume Daniel, Udo Schmidt-Edelkraut, Dietmar Spengler, Anke Hoffmann, Max Planck Institute of Psychiatry, Translational Research, 80804 Munich, Germany. |
| Abstrakt: |
Neural stem cells (NSCs) and imprinted genes play an important role in brain development. On historical grounds, these two determinants have been largely studied independently of each other. Recent evidence suggests, however, that NSCs can reset select genomic imprints to prevent precocious depletion of the stem cell reservoir. Moreover, imprinted genes like the transcriptional regulator Zac1 can fine tune neuronal vs astroglial differentiation of NSCs. Zac1 binds in a sequence-specific manner to pro-neuronal and imprinted genes to confer transcriptional regulation and furthermore coregulates members of the p53-family in NSCs. At the genome scale, Zac1 is a central hub of an imprinted gene network comprising genes with an important role for NSC quiescence, proliferation and differentiation. Overall, transcriptional, epigenomic, and genomic mechanisms seem to coordinate the functional relationships of NSCs and imprinted genes from development to maturation, and possibly aging. |
