Developmental regulation of Erk signaling by mitotic kinases
- Datum
- 18.05.2026
- Zeit
- 14:00 - 15:00
- Sprecher
- Fei Chen
- Zugehörigkeit
- MPI for Molecular Biomedicine, Münster
- Sprache
- en
- Hauptthema
- Biologie
- Host
- Jesse Veenvliet
- Beschreibung
- During the peri-implantation phase of murine embryogenesis, the epiblast proliferates rapidly and undergoes epithelialization. At the same time, the preimplantation pluripotent state transforms into a more developmentally advanced, pregastrulation state. While extensive research has elucidated cell- extrinsic signals that direct the developmental progression, such as the Fgf/Mek/Erk pathway, the potential interplay of intrinsic cellular cues remains largely unexplored. To address this, we conducted a comprehensive phenotypic screen using an in vitro model of epiblast development. We identified aurora kinase A as a cell- intrinsic factor contributing to Erk activation and transcriptional response. Consequently, suppressing aurora kinase A activity delayed exit from naïve pluripotency. Moreover, our results show that upon entry into mitosis, Erk relocates to the cell division machinery. We found that in dividing cells, a fraction of Erk, with yet elusive functions, localizes on the centrosomes, where its phosphorylation depends on polo-like kinase 1.
Letztmalig verändert: 15.05.2026, 07:36:41
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Max Planck Institute of Molecular Cell Biology and Genetics (MPI-CBG CBG Galleria II (VC))Pfotenhauerstraße10801307Dresden
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- +49 351 210-0
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- +49 351 210-2000
- MPI-CBG
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- http://www.mpi-cbg.de
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Max Planck Institute of Molecular Cell Biology and GeneticsPfotenhauerstraße10801307Dresden
- Telefon
- +49 351 210-0
- Fax
- +49 351 210-2000
- MPI-CBG
- Homepage
- http://www.mpi-cbg.de
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