The Journal of Cell Biology · 2008 · 207 citations · 23 references
Life SciencesCell BiologyMolecular BiologyChromatin BiologyChromatin StructureNuclear OrganizationChromatinChromosome CondensationEndomembrane SystemMitosisNuclear ArchitectureNuclear EnvelopeChromatin ReorganizationMorphological RestructuringNuclear Envelope AssemblyNuclear Envelope ExpansionNuclear Envelope ProteinsNuclear Envelope StructureNuclear UltrastructureTime-lapse Microscopy
During mitosis, chromosomes are re‑enclosed by a nuclear envelope that is continuous with the endoplasmic reticulum, and recent in vitro work suggests that chromatin drives reorganization of tubular ER into the envelope, though the underlying principles remain unclear. The authors aim to quantitatively analyze nuclear membrane assembly in mammalian cells. They employ time‑lapse microscopy to monitor the process. ER tubule recruitment to chromatin completes nuclear envelope formation in about 12 minutes, and manipulation of reticulon and DP1 levels shows that conversion of ER tubules into sheets is the rate‑limiting step, demonstrating that ER‑shaping proteins drive nuclear envelope reconstruction in vivo.
During mitosis in metazoans, segregated chromosomes become enclosed by the nuclear envelope (NE), a double membrane that is continuous with the endoplasmic reticulum (ER). Recent in vitro data suggest that NE formation occurs by chromatin-mediated reorganization of the tubular ER; however, the basic principles of such a membrane-reshaping process remain uncharacterized. Here, we present a quantitative analysis of nuclear membrane assembly in mammalian cells using time-lapse microscopy. From the initial recruitment of ER tubules to chromatin, the formation of a membrane-enclosed, transport-competent nucleus occurs within approximately 12 min. Overexpression of the ER tubule-forming proteins reticulon 3, reticulon 4, and DP1 inhibits NE formation and nuclear expansion, whereas their knockdown accelerates nuclear assembly. This suggests that the transition from membrane tubules to sheets is rate-limiting for nuclear assembly. Our results provide evidence that ER-shaping proteins are directly involved in the reconstruction of the nuclear compartment and that morphological restructuring of the ER is the principal mechanism of NE formation in vivo.
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