Programmed cell death in the aspergilli and other filamentous fungi

References

• Strasser A, O'Connor L, Dixit VM. Apoptosis signaling. Annu Rev Biochem 2000; 69: 217–245
   PubMed Web of Science ®Google Scholar
• Kaufmann SH, Hengartner MO. Programmed cell death: alive and well in the new millennium. Trends Cell Biol 2001; 11: 526–534
   PubMed Web of Science ®Google Scholar
• Miller LK. Baculovirus interaction with host apoptotic pathways. J Cell Physiol 1997; 173: 178–182
   PubMed Web of Science ®Google Scholar
• Metzstein M, Stanfield G, Horvitz H. Genetics of programmed cell death in C. elegans: Past, present and future. Trends Genet 1998; 14: 410–416
   PubMed Web of Science ®Google Scholar
• Lam E, Kato N, Lawton M. Programmed cell death, mitochondria and the plant hypersensitive response. Nature 2001; 411: 848–853
   PubMed Web of Science ®Google Scholar
• Liu Y, Schiff M, Czymmek K, et al. Autophagy regulates programmed cell death during the plant innate immune response. Cell 2005; 121: 567–577
   PubMed Web of Science ®Google Scholar
• Fröhlich K-U, Madeo F. Apoptosis in yeast – a monocellular organism exhibits altruistic behaviour. FEBS Letters 2000; 473: 6–9
   PubMed Web of Science ®Google Scholar
• Madeo F, Engelhardt S, Herker E, et al. Apoptosis in yeast: a new model system with applications in cell biology and medicine. Curr Genet 2002; 41: 208–216
   PubMed Web of Science ®Google Scholar
• Ludovico P, Madeo F, Silva MT. Yeast programmed cell death: an intricate puzzle. IUBMB Life 2005; 57: 129–135
   PubMed Web of Science ®Google Scholar
• Madeo F, Frohlich E, Ligr M, et al. Oxygen stress: a regulator of apoptosis in yeast. J Cell Biol 1999; 145: 757–767
   PubMed Web of Science ®Google Scholar
• Ludovicho P, Sousa MJ, Siva MT, et al. Saccharomyces cerevisiae commits to a programmed cell death process in response to acetic acid. Microbiology 2001; 147: 2409–2415
   PubMed Web of Science ®Google Scholar
• Del Carratore R, Della Croce C, Simili M, et al. Cell cycle and morphological alterations as indicative of apoptosis promoted by UV irradiation in S. cerevisiae. Mutat Res Genet Toxicol Environ Mutagen 2002; 513: 183–191
   PubMed Web of Science ®Google Scholar
• Granot D, Levine A, Dor-Hefetz E. Sugar-induced apoptosis in yeast cells. FEMS Yeast Res 2003; 4: 7–13
   PubMed Web of Science ®Google Scholar
• Balzan R, Sapienza K, Galea DR, et al. Aspirin commits yeast cells to apoptosis depending on carbon source. Microbiology 2004; 150: 109–115
   PubMed Web of Science ®Google Scholar
• Silva RD, Sotoca R, Johansson B, et al. Hyperosmotic stress induces metacaspase- and mitochondria-dependent apoptosis in Saccharomyces cerevisiae. Mol Microbiol 2005; 58: 824–834
   PubMed Web of Science ®Google Scholar
• Hauptmann P, Riel C, Kunz-Schughart LA, et al. Defects in N-glycosylation induce apoptosis in yeast. Mol Microbiol 2006; 59: 765–778
   PubMed Web of Science ®Google Scholar
• Madeo F, Herker E, Maldener C, et al. A caspase-related protease regulates apoptosis in yeast. Mol Cell 2002; 9: 911–917
   PubMed Web of Science ®Google Scholar
• Herker E, Jungwirth H, Lehmann KA, et al. Chronological ageing leads to apoptosis in yeast. J Cell Biol 2004; 164: 501–507
   PubMed Web of Science ®Google Scholar
• Fannjiang Y, Cheng WC, Lee SJ, et al. Mitochondrial fusion proteins regulate programmed cell death in yeast. Genes Dec 2004; 18: 2785–2797
   PubMed Web of Science ®Google Scholar
• Wadskog I, Maldener C, Proksch A, et al. Yeast lacking SR07/SOP1-encoded tumor suppressor homologue show increased susceptibility to apoptosis-like cell death on exposure to NaCl stress. Mol Biol Cell 2004; 15: 1436–1444
   PubMed Web of Science ®Google Scholar
• Vanovska I, Hardwick JM. Viruses activate a genetically conserved cell death pathway in a unicellular organism. J Cell Biol 2005; 170: 391–399
   PubMed Web of Science ®Google Scholar
• Váchová L, Palková Z. Physiological regulation of yeast cell death in multicellular colonies is triggered by ammonia. J Cell Biol 2005; 169: 711–715
   PubMed Web of Science ®Google Scholar
• Wissing S, Ludovico P, Herker E, et al. An AIF orthologue regulates apoptosis in yeast. J Cell Biol 2004; 166: 969–974
   PubMed Web of Science ®Google Scholar
• Ludovico O, Rodrigues F, Almeida A, et al. Cytochrome c release and mitochondrial involvement in programmed cell death induced by acetic acid in Saccharomyces cerevisiae. Mol Biol Cell 2002; 13: 2598–2606
   PubMed Web of Science ®Google Scholar
• Severin FF, Hyman AA. Pheromone induces programmed cell death in S. cerevisiae. Curr Biol 2002; 12: R233–235
   PubMed Web of Science ®Google Scholar
• Li W, Sun L, Liang Q, et al. Yeast AMID homologue Ndi1p displays respiration-restricted apoptotic activity and is involved in chronological ageing. Mol Biol Cell 2006; 17: 1802–1811
   PubMed Web of Science ®Google Scholar
• Laun P, Pichova A, Madeo F, et al. Aged mother cells of Saccharomyces cerevisiae show markers of oxidative stress and apoptosis. Mol Microbiol 2001; 39: 1166–1173
   PubMed Web of Science ®Google Scholar
• Mazzoni C, Mancini L, Verdone F, et al. Atruncated form of KILsm4p and the absence of factors involved in mRNA decapping trigger apoptosis in yeast. Mol Biol Cell 2003; 14: 721–729
   PubMed Web of Science ®Google Scholar
• Weinberger M, Ramachandran L, Burhans WC. Apoptosis in yeasts. IUBMB Life 2003; 55: 467–472
   PubMed Web of Science ®Google Scholar
• Machida K, Tanaka T, Fujita K, et al. Farnesol-induced generation of reactive oxygen species via indirect inhibition of the mitochondrial electron transport chain in the yeast Saccharomyces cerevisiae. J Bacteriol 1998; 180: 4460–4465
   PubMed Web of Science ®Google Scholar
• Fujita KI, Tani K, Usuki Y, et al. Growth inhibition dependent on reactive oxygen species generated by C9-UK-2A, a derivative of the antifungal antibiotic UK-2A, in Saccharomyces cerevisae. J Antibiot 2004; 57: 511–517
   PubMed Web of Science ®Google Scholar
• Brace JL, Van der Weele DJ, Rudin CM. SvfI inhibits reactive oxygen species generation and promotes survival under conditions of oxidative stress in Saccharomyces cerevisiae. Yeast 2005; 22: 641–652
   PubMed Web of Science ®Google Scholar
• Weinberger M, Ramachandran L, Feng L, et al. Apoptosis in budding yeast caused by defects in initiation of DNA replication. J Cell Sci 2005; 118: 3543–3553
   PubMed Web of Science ®Google Scholar
• Mazzoni C, Herker E, Palermo V, et al. Yeast caspase 1 links messenger RNA stability to apoptosis in yeast. EMBO Rep 2005; 6: 1076–1081
   Google Scholar
• Gourlay CW, Ayscough KR. A role for actin in aging and apoptosis. Biochem Soc Trans 2005; 33: 1260–1264
   PubMedGoogle Scholar
• Fedorova ND, Badger JH, Robson GD, et al. Comparative analysis of programmed cell death pathways in filamentous fungi. BMC Genomics 2005; 6: 177
   Google Scholar
• Leipe DD, Koonin EV, Aravind L. STAND, a class of P-loop NTPases including animal and plant regulators of programmed cell death: multiple, complex domain architectures, unusual phyletic patterns, and evolution by horizontal gene transfer. J Mol Biol 2004; 343: 1–28
   PubMed Web of Science ®Google Scholar
• Hong SJ, Dawson TM, Dawson VL. Nuclear and mitochondrial conversations in cell death: PARP-1 and AIF signaling. Trends Pharmacol Sci 2004; 25: 259–264
   PubMed Web of Science ®Google Scholar
• Trinci AP, Righelato RC. Changes in constituents and ultrastructure of hyphal compartments during autolysis of glucose-starved Penicillium chrysogenum. J Gen Microbiol 1970; 60: 239–249
   PubMedGoogle Scholar
• White S, McIntyre M, Berry DR, et al. The autolysis of industrial filamentous fungi. Crit Rev Biotechnol 2002; 22: 1–14
   PubMed Web of Science ®Google Scholar
• Hernawan T, Fleet G. Chemical and cytological changes during the autolysis of yeasts. J Ind Microbiol 1995; 14: 440–450
   PubMedGoogle Scholar
• McNeil B, Berry DR, Harvey LM, et al. Measurement of autolysis in submerged batch cultures of Penicillium chrysogenum. Biotechnol Bioeng 1998; 57: 297–305
   PubMed Web of Science ®Google Scholar
• McIntyre M, Berry DR, McNeil B. Role of proteases in autolysis of Penicillium chrysogenum chemostat cultures in response to nutrient depletion. Appl Microbiol Biotechnol 2000; 53: 235–242
   PubMed Web of Science ®Google Scholar
• Mousavi SA, Robson GD. Entry into the stationary phase is associated with a rapid loss of viability and an apoptotic-like phenotype in the opportunistic pathogen Aspergillus fumigatus. Fungal Genet Biol 2003; 39: 221–229
   PubMed Web of Science ®Google Scholar
• Emri T, Molnár Z, Pócsi I. The appearances of autolytic and apoptotic markers are concomitant but differently regulated in carbon-starving Aspergillus nidulans cultures. FEMS Microbiol Lett 2005; 251: 297–303
   PubMed Web of Science ®Google Scholar
• Mousavi SA, Robson GD. Oxidative and amphotericin B-mediated cell death in the opportunistic pathogen Aspergillus fumigatus is associated with an apoptotic-like phenotype. Microbiology 2004; 150: 1937–1945
   PubMed Web of Science ®Google Scholar
• Cheng J, Park TS, Chio LC, et al. Induction of apoptosis by sphingoid long-chain bases in Aspergillus nidulans. Mol Cell Biol 2003; 23: 163–177
   PubMed Web of Science ®Google Scholar
• Leiter E, Szappanos H, Oberparleiter C, et al. Antifungal protein PAF severely affects the integrity of the plasma membrane of Aspergillus nidulans and induces an apoptosis-like phenotype. Antimicrob Agents Chemother 2005; 49: 2445–24453
   PubMed Web of Science ®Google Scholar
• Semighini CP, Hornby JM, Dumitru R, et al. Farnesol-induced apoptosis in Aspergillus nidulansreveals a possible mechanism for antagonistic interactions between fungi. Mol Microbiol 2006; 59: 753–764
   PubMed Web of Science ®Google Scholar
• Glass NL, Jacobson DJ, Shiu PK. The genetics of hyphal fusion and vegetative incompatibility in filamentous ascomycete fungi. Annu Rev Genet 2000; 34: 165–186
   PubMed Web of Science ®Google Scholar
• Saupe SJ: Molecular genetics of heterokaryon incompatibility in filamentous ascomycetes. Microbiol Mol Biol Rev 2000; 64: 489–502.
   PubMed Web of Science ®Google Scholar
• Saupe SJ, Clave C, Begueret J. Vegetative incompatibility in filamentous fungi: Podospora and Neurospora provide some clues. Curr Opin Microbiol 2000; 3: 608–612
   PubMed Web of Science ®Google Scholar
• Umar MH, Van Griensven LJLD. Morphogenetic cell death in developing primordia of Agaricus bisporus. Mycologia 1997; 89: 274–277
   Web of Science ®Google Scholar
• Umar MH, Van Griensven LJLD. The role of morphogenetic cell death in the histogenesis of the mycelial cord of Agaricus bisporus and in the development of macrofungi. Mycol Res 1998; 102: 719–735
   Google Scholar
• Lu BC, Gallo N, Kues U. White-cap mutants and meiotic apoptosis in the basidiomycete Coprinus cinereus. Fung Genet Biol 2003; 39: 82–93
   PubMed Web of Science ®Google Scholar
• Thrane C, Kaufmann U, Stummann BM, et al. Activation of caspase-like activity and poly (ADP-ribose) polymerase degradation during sporulation in Aspergillus nidulans. Fung Genet Biol 2004; 41: 361–368
   PubMed Web of Science ®Google Scholar
• Chen C, Dickman MB. Proline suppresses apoptosis in the fungal pathogen Colletotrichum trifolii. Proc Natl Acad Sci USA 2005; 102: 3459–3464
   PubMed Web of Science ®Google Scholar
• Phillips AJ, Crowe JD, Ramsdale M. Ras pathway signaling accelerates programmed cell death in the pathogenic fungus Candida albicans. Proc Natl Acad Sci USA 2006; 103: 726–731
   PubMed Web of Science ®Google Scholar
• Marek SM, Wu J, Glass LN, et al. Nuclear DNA degradation during heterokaryon incompatibility in Neurosporia crassa. Fung Genet Biol 2003; 40: 126–137
   PubMed Web of Science ®Google Scholar