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      Apoptotic-like programed cell death in fungi: the benefits in filamentous species

      research-article
      , ,
      Frontiers in Oncology
      Frontiers Research Foundation
      apoptosis, botrytis, fungi, PCD, Saccharomyces

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          Abstract

          Studies conducted in the early 1990s showed for the first time that Saccharomyces cerevisiae can undergo cell death with hallmarks of animal apoptosis. These findings came as a surprise, since suicide machinery was unexpected in unicellular organisms. Today, apoptosis in yeast is well-documented. Apoptotic death of yeast cells has been described under various conditions and S. cerevisiae homologs of human apoptotic genes have been identified and characterized. These studies also revealed fundamental differences between yeast and animal apoptosis; in S. cerevisiae apoptosis is mainly associated with aging and stress adaptation, unlike animal apoptosis, which is essential for proper development. Further, many apoptosis regulatory genes are either missing, or highly divergent in S. cerevisiae. Therefore, in this review we will use the term apoptosis-like programed cell death (PCD) instead of apoptosis. Despite these significant differences, S. cerevisiae has been instrumental in promoting the study of heterologous apoptotic proteins, particularly from human. Work in fungi other than S. cerevisiae revealed differences in the manifestation of PCD in single cell (yeasts) and multicellular (filamentous) species. Such differences may reflect the higher complexity level of filamentous species, and hence the involvement of PCD in a wider range of processes and life styles. It is also expected that differences might be found in the apoptosis apparatus of yeast and filamentous species. In this review we focus on aspects of PCD that are unique or can be better studied in filamentous species. We will highlight the similarities and differences of the PCD machinery between yeast and filamentous species and show the value of using S. cerevisiae along with filamentous species to study apoptosis.

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          Nonfilamentous C. albicans mutants are avirulent.

          Candida albicans and Saccharomyces cerevisiae switch from a yeast to a filamentous form. In Saccharomyces, this switch is controlled by two regulatory proteins, Ste12p and Phd1p. Single-mutant strains, ste12/ste12 or phd1/phd1, are partially defective, whereas the ste12/ste12 phd1/phd1 double mutant is completely defective in filamentous growth and is noninvasive. The equivalent cph1/cph1 efg1/efg1 double mutant in Candida (Cph1p is the Ste12p homolog and Efg1p is the Phd1p homolog) is also defective in filamentous growth, unable to form hyphae or pseudohyphae in response to many stimuli, including serum or macrophages. This Candida cph1/cph1 efg1/efg1 double mutant, locked in the yeast form, is avirulent in a mouse model.
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            Autophagic fungal cell death is necessary for infection by the rice blast fungus.

            Rice blast is caused by the fungus Magnaporthe grisea, which elaborates specialized infection cells called appressoria to penetrate the tough outer cuticle of the rice plant Oryza sativa. We found that the formation of an appressorium required, sequentially, the completion of mitosis, nuclear migration, and death of the conidium (fungal spore) from which the infection originated. Genetic intervention during mitosis prevented both appressorium development and conidium death. Impairment of autophagy, by the targeted mutation of the MgATG8 gene, arrested conidial cell death but rendered the fungus nonpathogenic. Thus, the initiation of rice blast requires autophagic cell death of the conidium.
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              Penetration of hard substrates by a fungus employing enormous turgor pressures.

              Many fungal pathogens penetrate plant leaves from a specialized cell called an appressorium. The rice blast pathogen Magnaporthe grisea can also penetrate synthetic surfaces such as poly(vinyl chloride). Previous experiments have suggested that penetration requires an elevated appressorial turgor pressure. In the present report we have used nonbiodegradable Mylar membranes, exhibiting a range of surface hardness, to test the proposition that penetration is driven by turgor. Reducing appressorial turgor by osmotic stress inhibited penetration of these membranes. The size of the turgor deficit required to inhibit penetration was a function of the surface hardness. Penetration of the hardest membranes was inhibited by small decreases in appressorial turgor, while penetration of the softer membranes was sensitive only to large decreases in turgor. Similarly, penetration of the host surface was inhibited in a manner comparable to penetration of the hardest Mylar membranes. Indirect measurements of turgor, obtained through osmotically induced collapse of appressoria, indicated that the infection apparatus can generate turgor pressures in excess of 8.0 MPa (80 bars). We conclude that penetration of synthetic membranes, and host epidermal cells, is accomplished by application of the physical force derived from appressorial turgor.
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                Author and article information

                Journal
                Front Oncol
                Front Oncol
                Front. Oncol.
                Frontiers in Oncology
                Frontiers Research Foundation
                2234-943X
                07 August 2012
                2012
                : 2
                : 97
                Affiliations
                simpleDepartment of Molecular Biology and Ecology of Plants, Tel Aviv University, Tel Aviv, Israel
                Author notes

                Edited by: Manuela Côrte-Real, Universidade do Minho, Portugal

                Reviewed by: Gustavo Henrique Goldman, Universidade de Sao Paulo, Brazil Heinz D. Osiewacz, Goethe University, Germany Sathish Kumar Mungamuri, Mount Sinai School of Medicine, USA

                *Correspondence: Amir Sharon, Department of Molecular Biology and Ecology of Plants, Tel Aviv University, Tel Aviv 69978, Israel. e-mail: amirsh@ 123456ex.tau.ac.il
                Neta Shlezinger and Nir Goldfinger have contributed equally to this work.

                This article was submitted to Frontiers in Molecular and Cellular Oncology, a specialty of Frontiers in Oncology.

                Article
                10.3389/fonc.2012.00097
                3412994
                22891165
                d1e2dfb1-07c4-406f-8840-5a6523b24724
                Copyright © Shlezinger, Goldfinger and Sharon.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.

                History
                : 29 April 2012
                : 23 July 2012
                Page count
                Figures: 0, Tables: 0, Equations: 0, References: 102, Pages: 8, Words: 0
                Categories
                Oncology
                Review Article

                Oncology & Radiotherapy
                botrytis,saccharomyces,pcd,fungi,apoptosis
                Oncology & Radiotherapy
                botrytis, saccharomyces, pcd, fungi, apoptosis

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