spacer gif spacer gif spacer gif spacer gif spacer gif
 QUICK SEARCH:   [advanced]


spacer gif
     Home     Help     Feedback     Subscriptions     Archive     Search     Table of Contents    


This Article
Right arrow Full Text (PDF)
Right arrow References
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Hinchcliffe, E. H.
Right arrow Articles by Sluder, G.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Hinchcliffe, E. H.
Right arrow Articles by Sluder, G.

Journal of Cell Science, Vol 112, Issue 8 1139-1148, Copyright © 1999 by Company of Biologists


JOURNAL ARTICLES

Nucleo-cytoplasmic interactions that control nuclear envelope breakdown and entry into mitosis in the sea urchin zygote

EH Hinchcliffe, EA Thompson, FJ Miller, J Yang and G Sluder
Department of Cell Biology, University of Massachusetts Medical School, Worcester, MA 01605, USA.

In sea urchin zygotes and mammalian cells nuclear envelope breakdown (NEB) is not driven simply by a rise in cytoplasmic cyclin dependent kinase 1-cyclin B (Cdk1-B) activity; the checkpoint monitoring DNA synthesis can prevent NEB in the face of mitotic levels of Cdk1-B. Using sea urchin zygotes we investigated whether this checkpoint prevents NEB by restricting import of regulatory proteins into the nucleus. We find that cyclin B1-GFP accumulates in nuclei that cannot complete DNA synthesis and do not break down. Thus, this checkpoint limits NEB downstream of both the cytoplasmic activation and nuclear accumulation of Cdk1-B1. In separate experiments we fertilize sea urchin eggs with sperm whose DNA has been covalently cross-linked to inhibit replication. When the pronuclei fuse, the resulting zygote nucleus does not break down for >180 minutes (equivalent to three cell cycles), even though Cdk1-B activity rises to greater than mitotic levels. If pronuclear fusion is prevented, then the female pronucleus breaks down at the normal time (average 68 minutes) and the male pronucleus with cross-linked DNA breaks down 16 minutes later. This male pronucleus has a functional checkpoint because it does not break down for >120 minutes if the female pronucleus is removed just prior to NEB. These results reveal the existence of an activity released by the female pronucleus upon its breakdown, that overrides the checkpoint in the male pronucleus and induces NEB. Microinjecting wheat germ agglutinin into binucleate zygotes reveals that this activity involves molecules that must be actively translocated into the male pronucleus.


This article has been cited by other articles:


Home page
J. Cell Biol.Home page
A. S. Gladfelter, A. K. Hungerbuehler, and P. Philippsen
Asynchronous nuclear division cycles in multinucleated cells
J. Cell Biol., January 30, 2006; 172(3): 347 - 362.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
R. Philipova, J. Kisielewska, P. Lu, M. Larman, J.-Y. Huang, and M. Whitaker
ERK1 activation is required for S-phase onset and cell cycle progression after fertilization in sea urchin embryos
Development, February 1, 2005; 132(3): 579 - 589.
[Abstract] [Full Text] [PDF]


Home page
Hum ReprodHome page
S. Kattera and C. Chen
Developmental potential of human pronuclear zygotes in relation to their pronuclear orientation
Hum. Reprod., February 1, 2004; 19(2): 294 - 299.
[Abstract] [Full Text] [PDF]




© The Company of Biologists Ltd 1999