This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow E-mail 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 arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Moseley, J. B.
Right arrow Articles by Goode, B. L.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Moseley, J. B.
Right arrow Articles by Goode, B. L.

 Previous Article  |  Next Article 

Microbiology and Molecular Biology Reviews, September 2006, p. 605-645, Vol. 70, No. 3
1092-2172/06/$08.00+0     doi:10.1128/MMBR.00013-06
Copyright © 2006, American Society for Microbiology. All Rights Reserved.

The Yeast Actin Cytoskeleton: from Cellular Function to Biochemical Mechanism

James B. Moseley and Bruce L. Goode*

Department of Biology and The Rosenstiel Basic Medical Sciences Research Center, Brandeis University, Waltham, Massachusetts 02454

All cells undergo rapid remodeling of their actin networks to regulate such critical processes as endocytosis, cytokinesis, cell polarity, and cell morphogenesis. These events are driven by the coordinated activities of a set of 20 to 30 highly conserved actin-associated proteins, in addition to many cell-specific actin-associated proteins and numerous upstream signaling molecules. The combined activities of these factors control with exquisite precision the spatial and temporal assembly of actin structures and ensure dynamic turnover of actin structures such that cells can rapidly alter their cytoskeletons in response to internal and external cues. One of the most exciting principles to emerge from the last decade of research on actin is that the assembly of architecturally diverse actin structures is governed by highly conserved machinery and mechanisms. With this realization, it has become apparent that pioneering efforts in budding yeast have contributed substantially to defining the universal mechanisms regulating actin dynamics in eukaryotes. In this review, we first describe the filamentous actin structures found in Saccharomyces cerevisiae (patches, cables, and rings) and their physiological functions, and then we discuss in detail the specific roles of actin-associated proteins and their biochemical mechanisms of action.


* Corresponding author. Mailing address: Rosenstiel Center, Brandeis University, 415 South Street, Waltham, MA 02454. Phone: (781) 736-2464. Fax: (781) 736-2405. E-mail: goode{at}brandeis.edu.


Microbiology and Molecular Biology Reviews, September 2006, p. 605-645, Vol. 70, No. 3
1092-2172/06/$08.00+0     doi:10.1128/MMBR.00013-06
Copyright © 2006, American Society for Microbiology. All Rights Reserved.




This article has been cited by other articles:

  • Mata, J. (2010). Genome-wide mapping of myosin protein-RNA networks suggests the existence of specialized protein production sites. FASEB J. 24: 479-484 [Abstract] [Full Text]  
  • Maerz, S., Funakoshi, Y., Negishi, Y., Suzuki, T., Seiler, S. (2010). The Neurospora Peptide:N-Glycanase Ortholog PNG1 Is Essential for Cell Polarity despite Its Lack of Enzymatic Activity. J. Biol. Chem. 285: 2326-2332 [Abstract] [Full Text]  
  • Rohn, J. L., Baum, B. (2010). Actin and cellular architecture at a glance. J. Cell Sci. 123: 155-158 [Full Text]  
  • Gale, C. A., Leonard, M. D., Finley, K. R., Christensen, L., McClellan, M., Abbey, D., Kurischko, C., Bensen, E., Tzafrir, I., Kauffman, S., Becker, J., Berman, J. (2009). SLA2 mutations cause SWE1-mediated cell cycle phenotypes in Candida albicans and Saccharomyces cerevisiae. Microbiology 155: 3847-3859 [Abstract] [Full Text]  
  • Geymonat, M., Spanos, A., de Bettignies, G., Sedgwick, S. G. (2009). Lte1 contributes to Bfa1 localization rather than stimulating nucleotide exchange by Tem1. JCB 187: 497-511 [Abstract] [Full Text]  
  • Yamaguchi, M., Kopecka, M. (2009). Ultrastructural disorder of the secretory pathway in temperature-sensitive actin mutants of Saccharomyces cerevisiae. J Electron Microsc (Tokyo) 0: dfp050v1-dfp050 [Abstract] [Full Text]  
  • Huttenhower, C., Hibbs, M. A., Myers, C. L., Caudy, A. A., Hess, D. C., Troyanskaya, O. G. (2009). The impact of incomplete knowledge on evaluation: an experimental benchmark for protein function prediction. Bioinformatics 25: 2404-2410 [Abstract] [Full Text]  
  • Slaughter, B. D., Smith, S. E., Li, R. (2009). Symmetry Breaking in the Life Cycle of the Budding Yeast. Cold Spring Harb. Perspect. Biol. 1: a003384-a003384 [Abstract] [Full Text]  
  • Tessarz, P., Schwarz, M., Mogk, A., Bukau, B. (2009). The Yeast AAA+ Chaperone Hsp104 Is Part of a Network That Links the Actin Cytoskeleton with the Inheritance of Damaged Proteins. Mol. Cell. Biol. 29: 3738-3745 [Abstract] [Full Text]  
  • Burston, H. E., Maldonado-Baez, L., Davey, M., Montpetit, B., Schluter, C., Wendland, B., Conibear, E. (2009). Regulators of yeast endocytosis identified by systematic quantitative analysis. JCB 185: 1097-1110 [Abstract] [Full Text]  
  • Goranov, A. I., Cook, M., Ricicova, M., Ben-Ari, G., Gonzalez, C., Hansen, C., Tyers, M., Amon, A. (2009). The rate of cell growth is governed by cell cycle stage. Genes Dev. 23: 1408-1422 [Abstract] [Full Text]  
  • Gao, L., Bretscher, A. (2009). Polarized Growth in Budding Yeast in the Absence of a Localized Formin. Mol. Biol. Cell 20: 2540-2548 [Abstract] [Full Text]  
  • He, Y., Linder, M. E. (2009). Differential palmitoylation of the endosomal SNAREs syntaxin 7 and syntaxin 8. J. Lipid Res. 50: 398-404 [Abstract] [Full Text]  
  • Stokasimov, E., McKane, M., Rubenstein, P. A. (2008). Role of Intermonomer Ionic Bridges in the Stabilization of the Actin Filament. J. Biol. Chem. 283: 34844-34854 [Abstract] [Full Text]  
  • Delgehyr, N., Lopes, C. S. J., Moir, C. A., Huisman, S. M., Segal, M. (2008). Dissecting the involvement of formins in Bud6p-mediated cortical capture of microtubules in S. cerevisiae. J. Cell Sci. 121: 3803-3814 [Abstract] [Full Text]  
  • Nikitin, D., Tosato, V., Zavec, A. B., Bruschi, C. V. (2008). Cellular and molecular effects of nonreciprocal chromosome translocations in Saccharomyces cerevisiae. Proc. Natl. Acad. Sci. USA 105: 9703-9708 [Abstract] [Full Text]  
  • Daugherty, K. M., Goode, B. L. (2008). Functional Surfaces on the p35/ARPC2 Subunit of Arp2/3 Complex Required for Cell Growth, Actin Nucleation, and Endocytosis. J. Biol. Chem. 283: 16950-16959 [Abstract] [Full Text]  
  • Gheorghe, D. M., Aghamohammadzadeh, S., Rooij, I. I. S.-d., Allwood, E. G., Winder, S. J., Ayscough, K. R. (2008). Interactions between the Yeast SM22 Homologue Scp1 and Actin Demonstrate the Importance of Actin Bundling in Endocytosis. J. Biol. Chem. 283: 15037-15046 [Abstract] [Full Text]  
  • Gao, L., Bretscher, A. (2008). Analysis of Unregulated Formin Activity Reveals How Yeast Can Balance F-Actin Assembly between Different Microfilament-based Organizations. Mol. Biol. Cell 19: 1474-1484 [Abstract] [Full Text]  
  • Yu, L., Qi, M., Sheff, M. A., Elion, E. A. (2008). Counteractive Control of Polarized Morphogenesis during Mating by Mitogen-activated Protein Kinase Fus3 and G1 Cyclin-dependent Kinase. Mol. Biol. Cell 19: 1739-1752 [Abstract] [Full Text]  
  • Rouiller, I., Xu, X.-P., Amann, K. J., Egile, C., Nickell, S., Nicastro, D., Li, R., Pollard, T. D., Volkmann, N., Hanein, D. (2008). The structural basis of actin filament branching by the Arp2/3 complex. JCB 180: 887-895 [Abstract] [Full Text]  
  • Querin, L., Sanvito, R., Magni, F., Busti, S., Van Dorsselaer, A., Alberghina, L., Vanoni, M. (2008). Proteomic Analysis of a Nutritional Shift-up in Saccharomyces cerevisiae Identifies Gvp36 as a BAR-containing Protein Involved in Vesicular Traffic and Nutritional Adaptation. J. Biol. Chem. 283: 4730-4743 [Abstract] [Full Text]  
  • Frederick, R. L., Okamoto, K., Shaw, J. M. (2008). Multiple Pathways Influence Mitochondrial Inheritance in Budding Yeast. Genetics 178: 825-837 [Abstract] [Full Text]  
  • Jin, M., Cai, M. (2008). A Novel Function of Arp2p in Mediating Prk1p-specific Regulation of Actin and Endocytosis in Yeast. Mol. Biol. Cell 19: 297-307 [Abstract] [Full Text]  
  • Mseka, T., Bamburg, J. R., Cramer, L. P. (2007). ADF/cofilin family proteins control formation of oriented actin-filament bundles in the cell body to trigger fibroblast polarization. J. Cell Sci. 120: 4332-4344 [Abstract] [Full Text]  
  • Isgandarova, S., Jones, L., Forsberg, D., Loncar, A., Dawson, J., Tedrick, K., Eitzen, G. (2007). Stimulation of Actin Polymerization by Vacuoles via Cdc42p-dependent Signaling. J. Biol. Chem. 282: 30466-30475 [Abstract] [Full Text]  
  • Wolyniak, M. J., Sundstrom, P. (2007). Role of Actin Cytoskeletal Dynamics in Activation of the Cyclic AMP Pathway and HWP1 Gene Expression in Candida albicans. Eukaryot Cell 6: 1824-1840 [Abstract] [Full Text]  
  • Okreglak, V., Drubin, D. G. (2007). Cofilin recruitment and function during actin-mediated endocytosis dictated by actin nucleotide state. JCB 178: 1251-1264 [Abstract] [Full Text]  
  • Gao, X.-D., Sperber, L. M., Kane, S. A., Tong, Z., Tong, A. H. Y., Boone, C., Bi, E. (2007). Sequential and Distinct Roles of the Cadherin Domain-containing Protein Axl2p in Cell Polarization in Yeast Cell Cycle. Mol. Biol. Cell 18: 2542-2560 [Abstract] [Full Text]  
  • Buttery, S. M., Yoshida, S., Pellman, D. (2007). Yeast Formins Bni1 and Bnr1 Utilize Different Modes of Cortical Interaction during the Assembly of Actin Cables. Mol. Biol. Cell 18: 1826-1838 [Abstract] [Full Text]  
  • Park, H.-O., Bi, E. (2007). Central Roles of Small GTPases in the Development of Cell Polarity in Yeast and Beyond. Microbiol. Mol. Biol. Rev. 71: 48-96 [Abstract] [Full Text]