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doi: 10.1242/10.1242/jcs.00136
Research Article |
1 Department of Physiology, University of Connecticut Health Center, Farmington,
CT 06032, USA
2 Marine Biological Laboratory, Woods Hole, MA 02543, USA
3 Department of Cell Biology and Howard Hughes Medical Institute, Harvard
Medical School, Boston, MA 02115, USA
4 European Molecular Biology Laboratory, Meyerhofstrasse 1, 69117 Heidelberg,
Germany
* Author for correspondence (e-mail: terasaki{at}neuron.uchc.edu)
Accepted 3 September 2002
Recent studies in Xenopus egg extracts indicate that the small G
protein Ran has a central role in spindle assembly and nuclear envelope
reformation. We determined Ran localization and dynamics in cells during M
phase. By immunofluorescence, Ran is accumulated on the chromosomes of
meiosis-II-arrested Xenopus eggs. In living cells, fluorescently
labeled Ran associated with the chromosomes in Xenopus and remained
associated during anaphase when eggs were artificially activated. Fluorescent
Ran associated with chromosomes in mouse eggs, during meiotic maturation and
early embryonic divisions in starfish, and to a lesser degree during mitosis
of a cultured mammalian cell line. Chromosomal Ran undergoes constant flux.
From photobleach experiments in immature starfish oocytes, chromosomal Ran has
a koff of
0.06 second-1, and binding analysis
suggests that there is a single major site. The chromosomal interactions may
serve to keep Ran-GTP in the vicinity of the chromosomes for spindle assembly
and nuclear envelope reformation.
Key words: Cell division, Chromosomes, G-proteins, Meiosis, Mitosis, Nuclear proteins
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