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Differential regulation of actin polymerization and structure by yeast formin isoforms
Journal article   Open access   Peer reviewed

Differential regulation of actin polymerization and structure by yeast formin isoforms

Kuo-Kuang Wen and Peter A Rubenstein
The Journal of biological chemistry, Vol.284(25), pp.16776-16783
06/19/2009
DOI: 10.1074/jbc.M109.006981
PMCID: PMC2719313
PMID: 19386598
url
https://doi.org/10.1074/jbc.M109.006981View
Published (Version of record) Open Access

Abstract

The budding yeast formins, Bnr1 and Bni1, behave very differently with respect to their interactions with muscle actin. However, the mechanisms underlying these differences are unclear, and these formins do not interact with muscle actin in vivo. We use yeast wild type and mutant actins to further assess these differences between Bnr1 and Bni1. Low ionic strength G-buffer does not promote actin polymerization. However, Bnr1, but not Bni1, causes the polymerization of pyrene-labeled Mg-G-actin in G-buffer into single filaments based on fluorometric and EM observations. Polymerization by Bnr1 does not occur with Ca-G-actin. By cosedimentation, maximum filament formation occurs at a Bnr1:actin ratio of 1:2. The interaction of Bnr1 with pyrene-labeled S265C Mg-actin yields a pyrene excimer peak, from the cross-strand interaction of pyrene probes, which only occurs in the context of F-actin. In F-buffer, Bnr1 promotes much faster yeast actin polymerization than Bni1. It also bundles the F-actin in contrast to the low ionic strength situation where only single filaments form. Thus, the differences previously observed with muscle actin are not actin isoform-specific. The binding of both formins to F-actin saturate at an equimolar ratio, but only about 30% of each formin cosediments with F-actin. Finally, addition of Bnr1 but not Bni1 to pyrene-labeled wild type and S265C Mg-F actins enhanced the pyrene- and pyrene-excimer fluorescence, respectively, suggesting Bnr1 also alters F-actin structure. These differences may facilitate the ability of Bnr1 to form the actin cables needed for polarized delivery of nutrients and organelles to the growing yeast bud.
Saccharomyces cerevisiae Proteins - ultrastructure Microscopy, Electron, Transmission Saccharomyces cerevisiae - genetics Multiprotein Complexes Actins - metabolism Actins - ultrastructure Saccharomyces cerevisiae Proteins - genetics Cytoskeletal Proteins - ultrastructure Actins - genetics Saccharomyces cerevisiae - metabolism Osmolar Concentration Saccharomyces cerevisiae Proteins - metabolism Actins - chemistry Protein Binding Cytoskeletal Proteins - metabolism Microfilament Proteins - metabolism Microfilament Proteins - ultrastructure Kinetics Mutation Saccharomyces cerevisiae Proteins - chemistry

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