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Quantitative kinetic analysis of nucleolar breakdown and reassembly during mitosis in live human cells. | LitMetric

Quantitative kinetic analysis of nucleolar breakdown and reassembly during mitosis in live human cells.

J Cell Biol

Division of Gene Regulation and Expression, School of Life Sciences, Wellcome Trust Biocentre, University of Dundee, Dundee DD1 5EH, Scotland, UK.

Published: September 2004

AI Article Synopsis

  • The study investigates how the nucleolus disassembles during cell division (mitosis) and reforms afterward, using advanced 4D microscopy with fluorescent tags.
  • It reveals the distinct behaviors of three nucleolar subcomponents during disassembly, particularly noting that RNA polymerase I subunits detach first before nuclear envelope breakdown.
  • The process of nucleolar reassembly is organized and follows a specific sequence, but the reaccumulation of components doesn't follow the same order as the disassembly.

Article Abstract

One of the great mysteries of the nucleolus surrounds its disappearance during mitosis and subsequent reassembly at late mitosis. Here, the relative dynamics of nucleolar disassembly and reformation were dissected using quantitative 4D microscopy with fluorescent protein-tagged proteins in human stable cell lines. The data provide a novel insight into the fates of the three distinct nucleolar subcompartments and their associated protein machineries in a single dividing cell. Before the onset of nuclear envelope (NE) breakdown, nucleolar disassembly started with the loss of RNA polymerase I subunits from the fibrillar centers. Dissociation of proteins from the other subcompartments occurred with faster kinetics but commenced later, coincident with the process of NE breakdown. The reformation pathway also follows a reproducible and defined temporal sequence but the order of reassembly is shown not to be dictated by the order in which individual nucleolar components reaccumulate within the nucleus after mitosis.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2172103PMC
http://dx.doi.org/10.1083/jcb.200405013DOI Listing

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