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 Buscemi, G.
Right arrow Articles by Carbone, M. L.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Buscemi, G.
Right arrow Articles by Carbone, M. L.

Journal of Cell Science, Vol 113, Issue 7 1199-1211, Copyright © 2000 by Company of Biologists


JOURNAL ARTICLES

The Saccharomyces cerevisiae SDA1 gene is required for actin cytoskeleton organization and cell cycle progression

G Buscemi, F Saracino, D Masnada and ML Carbone
Dipartimento di Genetica e di Biologia dei Microrganismi, Universita degli Studi di Milano, Milano, Italy.

The organization of the actin cytoskeleton is essential for several cellular processes. Here we report the characterization of a Saccharomyces cerevisiae novel gene, SDA1, encoding a highly conserved protein, which is essential for cell viability and is localized in the nucleus. Depletion or inactivation of Sda1 cause cell cycle arrest in G(1) by blocking both budding and DNA replication, without loss of viability. Furthermore, sda1-1 temperature-sensitive mutant cells arrest at the non-permissive temperature mostly without detectable structures of polymerized actin, although a normal actin protein level is maintained, indicating that Sda1 is required for proper organization of the actin cytoskeleton. To our knowledge, this is the first mutation shown to cause such a phenotype. Recovery of Sda1 activity restores proper assembly of actin structures, as well as budding and DNA replication. Furthermore we show that direct actin perturbation, either in sda1-1 or in cdc28-13 cells released from G(1) block, prevents recovery of budding and DNA replication. We also show that the block in G(1) caused by loss of Sda1 function is independent of Swe1. Altogether our results suggest that disruption of F-actin structure can block cell cycle progression in G(1) and that Sda1 is involved in the control of the actin cytoskeleton.


This article has been cited by other articles:


Home page
Mol. Biol. CellHome page
K. A. Bernstein and S. J. Baserga
The Small Subunit Processome Is Required for Cell Cycle Progression at G1
Mol. Biol. Cell, November 1, 2004; 15(11): 5038 - 5046.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
M. Dosil and X. R. Bustelo
Functional Characterization of Pwp2, a WD Family Protein Essential for the Assembly of the 90 S Pre-ribosomal Particle
J. Biol. Chem., September 3, 2004; 279(36): 37385 - 37397.
[Abstract] [Full Text] [PDF]


Home page
RNAHome page
A. FATICA, M. OEFFINGER, D. TOLLERVEY, and I. BOZZONI
Cic1p/Nsa3p is required for synthesis and nuclear export of 60S ribosomal subunits
RNA, December 1, 2003; 9(12): 1431 - 1436.
[Abstract] [Full Text] [PDF]


Home page
Mol. Biol. CellHome page
Z. A. Zimmerman and D. R. Kellogg
The Sda1 Protein Is Required for Passage through Start
Mol. Biol. Cell, January 1, 2001; 12(1): 201 - 219.
[Abstract] [Full Text]




© The Company of Biologists Ltd 2000