|
|
|
|
A more recent version of this article appeared on September 1, 2003
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Submitted on October 17, 2002
Accepted on May 14, 2003
1 Department of Biophysics and Biochemistry, Graduate School of
Science, University of Tokyo, Hongo, Tokyo 113-0033, Japan,
Genetic Dynamics Research Unit-Laboratory, The Institute
of Physical and Chemical Research (RIKEN), Wako-shi, Saitama 351-0198,
Japan
2 Department of Biophysics and Biochemistry, Graduate School of
Science, University of Tokyo, Hongo, Tokyo 113-0033, Japan
3 Genetic Dynamics Research Unit-Laboratory, The Institute
of Physical and Chemical Research (RIKEN), Wako-shi, Saitama 351-0198,
Japan, Cellular & Molecular Biology Laboratory, The
Institute of Physical and Chemical Research (RIKEN)/CREST of the JST,
Wako-shi, Saitama 351-0198, Japan
* Corresponding author. E-mail address: myamamot{at}ims.u-tokyo.ac.jp..
Fission yeast Cdc42p, a small GTPase of the Rho family, is essential for cell proliferation and maintenance of the rod-like cell morphology. Scd1/Ral1p is a GDP-GTP exchange factor (GEF) for Cdc42p. This study and a parallel study by others establish that Gef1p is another GEF for Cdc42p. Deletions of gef1 and scd1 are synthetically lethal, generating round dead cells, and hence mimic the phenotype of cdc42 deletion. Gef1p is localized mainly to the cell division site. Scd1p is also there, but it is also detectable in other parts of the cell, including the nucleus, growing ends, and the tips of conjugation tubes. Gef1p and Scd1p form a ring structure at the cell division site, which shrinks during cytokinesis following the contraction of the actomyosin ring. Formation of the Gef1p/Scd1p ring apparently depends on the integrity of the actomyosin ring. In turn, recruitment of Cdc42p to the cell division site follows the shrinking Gef1p/Scd1p ring; the Cdc42p accumulates like a closing iris. These observations suggest that Gef1p and Scd1p may have a role in mediating between contraction of the actomyosin ring and formation of the septum, by recruiting active Cdc42p to the septation site.
This article has been cited by other articles:
![]() |
M. Pinar, P. M. Coll, S. A. Rincon, and P. Perez Schizosaccharomyces pombe Pxl1 Is a Paxillin Homologue That Modulates Rho1 Activity and Participates in Cytokinesis Mol. Biol. Cell, April 1, 2008; 19(4): 1727 - 1738. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. Garcia, V. Tajadura, I. Garcia, and Y. Sanchez Rgf1p Is a Specific Rho1-GEF That Coordinates Cell Polarization with Cell Wall Biogenesis in Fission Yeast Mol. Biol. Cell, April 1, 2006; 17(4): 1620 - 1631. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. L. Morrell-Falvey, L. Ren, A. Feoktistova, G. D. Haese, and K. L. Gould Cell wall remodeling at the fission yeast cell division site requires the Rho-GEF Rgf3p J. Cell Sci., December 1, 2005; 118(23): 5563 - 5573. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Mutoh, K. Nakano, and I. Mabuchi Rho1-GEFs Rgf1 and Rgf2 are involved in formation of cell wall and septum, while Rgf3 is involved in cytokinesis in fission yeast Genes Cells, December 1, 2005; 10(12): 1189 - 1202. [Abstract] [Full Text] [PDF] |
||||
![]() |
V. Tajadura, B. Garcia, I. Garcia, P. Garcia, and Y. Sanchez Schizosaccharomyces pombe Rgf3p is a specific Rho1 GEF that regulates cell wall {beta}-glucan biosynthesis through the GTPase Rho1p J. Cell Sci., December 1, 2004; 117(25): 6163 - 6174. [Abstract] [Full Text] [PDF] |
||||