The de novo formation of the spore wall during the process of sporulation in the budding yeast S. cerevisiae provides a powerful, tractable model for the study of fungal cell wall assembly. This grant is focused on elucidating the structure and mechanism of assembly of the outer two layers of the spore wall. These two layers, comprised of the polysaccharide chitosan and the polyphenol dityrosine, are absent from vegetative cells and enable spores to resist a variety of environmental stresses. Importantly, although chitosan and dityrosine are absent from vegetative cell walls in budding yeast they are present in the walls of many pathogenic fungi such as Candida albicans. Chitosan and dityrosine are not found in mammalian extracellular matrices, meaning that drugs may be found that specifically inhibit fungal cell wall assembly without affecting mammalian cells. The budding yeast spore wall provides an excellent model system to study fungal wall morphogenesis. Experiments in this grant are divided into three interrelated aims: (1) define the composition and structure of the outer spore wall and elucidate the biosynthetic pathways by which the components are synthesized and incorporated into the spore wall;(2) elaborate on our studies which have indicated that dolichol, an essential lipid required for glycosylation in vegetative cells, has a novel role in coordinating outer spore wall formation and (3) apply the knowledge gained from our studies of spore wall assembly to define the conserved genetic toolkit essential for construction of the chitosan/dityrosine module of in cell walls of Candida albicans.
The wall of fungal cells surrounds the cell and is the interface between the cell and its environment. In pathogenic fungi, proper function of the cell wall is important for survival in the host and drugs targeting cell wall assembly are effective antifungal agents. The spores of baker's yeast Saccharomyces cerevisiae are not pathogenic but are surrounded by a complex coat, the spore wall, which includes many of the same components found in the walls of pathogenic fungi. We are using spore wall formation as a model system to unravel the biochemistry and genetics of fungal wall assembly. In particular, this application focuses on two polymers, chitosan and dityrosine, that are incorporated together into the wall. The chemical linkages between these polymers will be defined as well as the conserved genes required for their incorporation. The genes and activities identified in these studies will provide potential targets for the development of new antifungal drugs.
|Park, Jae-Sook; Thorsness, Mary K; Policastro, Robert et al. (2016) Yeast Vps13 promotes mitochondrial function and is localized at membrane contact sites. Mol Biol Cell 27:2435-49|
|Park, Jae-Sook; Halegoua, Simon; Kishida, Shosei et al. (2015) A conserved function in phosphatidylinositol metabolism for mammalian Vps13 family proteins. PLoS One 10:e0124836|
|Ucisik-Akkaya, Esma; Leatherwood, Janet K; Neiman, Aaron M (2014) A genome-wide screen for sporulation-defective mutants in Schizosaccharomyces pombe. G3 (Bethesda) 4:1173-82|
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|Park, Jae-Sook; Okumura, Yuuya; Tachikawa, Hiroyuki et al. (2013) SPO71 encodes a developmental stage-specific partner for Vps13 in Saccharomyces cerevisiae. Eukaryot Cell 12:1530-7|
|Park, Jae-Sook; Neiman, Aaron M (2012) VPS13 regulates membrane morphogenesis during sporulation in Saccharomyces cerevisiae. J Cell Sci 125:3004-11|
|Neiman, Aaron M (2011) Sporulation in the budding yeast Saccharomyces cerevisiae. Genetics 189:737-65|
|Suda, Yasuyuki; Rodriguez, Rachael K; Coluccio, Alison E et al. (2009) A screen for spore wall permeability mutants identifies a secreted protease required for proper spore wall assembly. PLoS One 4:e7184|
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