|Publication Type||Journal Article|
|Year of Publication||2014|
|Authors||Mori, M, Somogyi, K, Kondo, H, Monnier, N, Falk, HJ, Machado, P, Bathe, M, Nédélec, F, Lénárt, P|
|Date Published||2014 Jun 16|
|Keywords||Actin-Related Protein 2-3 Complex, Actinin, Actins, Animals, Meiosis, Molecular Sequence Data, Nuclear Envelope, Oocytes, Polymerization, Sequence Analysis, DNA, Starfish|
Animal cells disassemble and reassemble their nuclear envelopes (NEs) upon each division. Nuclear envelope breakdown (NEBD) serves as a major regulatory mechanism by which mixing of cytoplasmic and nuclear compartments drives the complete reorganization of cellular architecture, committing the cell for division. Breakdown is initiated by phosphorylation-driven partial disassembly of the nuclear pore complexes (NPCs), increasing their permeability but leaving the overall NE structure intact. Subsequently, the NE is rapidly broken into membrane fragments, defining the transition from prophase to prometaphase and resulting in complete mixing of cyto- and nucleoplasm. However, the mechanism underlying this rapid NE fragmentation remains largely unknown. Here, we show that NE fragmentation during NEBD in starfish oocytes is driven by an Arp2/3 complex-nucleated F-actin "shell" that transiently polymerizes on the inner surface of the NE. Blocking the formation of this F-actin shell prevents membrane fragmentation and delays entry of large cytoplasmic molecules into the nucleus. We observe spike-like protrusions extending from the F-actin shell that appear to "pierce" the NE during the fragmentation process. Finally, we show that NE fragmentation is essential for successful reproduction, because blocking this process in meiosis leads to formation of aneuploid eggs.
|Alternate Journal||Curr. Biol.|
|Grant List||P30 ES002109 / ES / NIEHS NIH HHS / United States|