|
|
|
|||
| Home Help Feedback Subscriptions Archive Search Table of Contents | ||||
Development, Vol 127, Issue 23 5021-5031, Copyright © 2000 by Company of Biologists
JOURNAL ARTICLES |
M Nakaya, A Fukui, Y Izumi, K Akimoto, M Asashima and S Ohno
Department of Molecular Biology, Yokohama City University School of Medicine, Yokohama 236-0004, Japan.
The asymmetric distribution of cellular components is an important clue for understanding cell fate decision during embryonic patterning and cell functioning after differentiation. In C. elegans embryos, PAR-3 and aPKC form a complex that colocalizes to the anterior periphery of the one-cell embryo, and are indispensable for anterior-posterior polarity that is formed prior to asymmetric cell division. In mammals, ASIP (PAR-3 homologue) and aPKCgamma form a complex and colocalize to the epithelial tight junctions, which play critical roles in epithelial cell polarity. Although the mechanism by which PAR-3/ASIP and aPKC regulate cell polarization remains to be clarified, evolutionary conservation of the PAR-3/ASIP-aPKC complex suggests their general role in cell polarity organization. Here, we show the presence of the protein complex in Xenopus laevis. In epithelial cells, XASIP and XaPKC colocalize to the cell-cell contact region. To our surprise, they also colocalize to the animal hemisphere of mature oocytes, whereas they localize uniformly in immature oocytes. Moreover, hormonal stimulation of immature oocytes results in a change in the distribution of XaPKC 2-3 hours after the completion of germinal vesicle breakdown, which requires the kinase activity of aPKC. These results suggest that meiotic maturation induces the animal-vegetal asymmetry of aPKC.
This article has been cited by other articles:
![]() |
O. Ossipova, J. Tabler, J. B. A. Green, and S. Y. Sokol PAR1 specifies ciliated cells in vertebrate ectoderm downstream of aPKC Development, December 1, 2007; 134(23): 4297 - 4306. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. D. Chalmers, M. Pambos, J. Mason, S. Lang, C. Wylie, and N. Papalopulu aPKC, Crumbs3 and Lgl2 control apicobasal polarity in early vertebrate development Development, March 1, 2005; 132(5): 977 - 986. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. Plusa, S. Frankenberg, A. Chalmers, A.-K. Hadjantonakis, C. A. Moore, N. Papalopulu, V. E. Papaioannou, D. M. Glover, and M. Zernicka-Goetz Downregulation of Par3 and aPKC function directs cells towards the ICM in the preimplantation mouse embryo J. Cell Sci., February 1, 2005; 118(3): 505 - 515. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. D. Chalmers, B. Strauss, and N. Papalopulu Oriented cell divisions asymmetrically segregate aPKC and generate cell fate diversity in the early Xenopus embryo Development, June 15, 2003; 130(12): 2657 - 2668. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Suzuki, K. Akimoto, and S. Ohno Protein Kinase C {lambda}/{iota} (PKC{lambda}/{iota}): A PKC Isotype Essential for the Development of Multicellular Organisms J. Biochem., January 1, 2003; 133(1): 9 - 16. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. E. Basham and L. S. Rose The Caenorhabditis elegans polarity gene ooc-5 encodes a Torsin-related protein of the AAA ATPase superfamily Development, November 15, 2001; 128(22): 4645 - 4656. [Abstract] [Full Text] [PDF] |
||||