
Centrosomes serve to organize new centrioles in cycling cells, whereas in quiescent cells they assemble primary cilia. We have recently shown that the mitochondrial porin VDAC3 is also a centrosomal protein that is predominantly associated with the mother centriole and modulates centriole assembly by recruiting Mps1 to centrosomes. Here, we show that depletion of VDAC3 causes inappropriate ciliogenesis in cycling cells, while expression of GFP-VDAC3 suppresses ciliogenesis in quiescent cells. Mps1 also negatively regulates ciliogenesis, and the inappropriate ciliogenesis caused by VDAC3 depletion can be bypassed by targeting Mps1 to centrosomes independently of VDAC3. Thus, our data show that a VDAC3-Mps1 module at the centrosome promotes ciliary disassembly during cell cycle entry and suppresses cilia assembly in proliferating cells. Our data also suggests that VDAC3 might be a link between mitochondrial dysfunction and ciliopathies in mammalian cells.
Centrosome, Serum, Organogenesis, Cell Cycle Proteins, Protein Serine-Threonine Kinases, Protein-Tyrosine Kinases, Mitochondrial Membrane Transport Proteins, Cell Line, Mitochondria, Protein Transport, Humans, Voltage-Dependent Anion Channels, Cilia, RNA, Small Interfering
Centrosome, Serum, Organogenesis, Cell Cycle Proteins, Protein Serine-Threonine Kinases, Protein-Tyrosine Kinases, Mitochondrial Membrane Transport Proteins, Cell Line, Mitochondria, Protein Transport, Humans, Voltage-Dependent Anion Channels, Cilia, RNA, Small Interfering
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| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Top 10% | |
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