Summary
We found a new type of morphogenesis in the plasmodia of the true slime moldPhysarum polycephalum: The plasmodium broke temporarily into pieces with uniform size at low temperatures. This fragmentation took place sharply around 5 h after the organism was transferred to low temperatures, and, unlike dormant spherulation, the fragments coalesced to recover the large plasmodium in about 15 h. Each fragment contained about 8 nuclei. The volume of the fragments remained constant under slight compression, but was halved under strong compression. The fragmentation showed a sharp temperature transition. The transition temperature was constant at 16 °C when plasmodia had been cultured above 16 °C, and decreased gradually as the culture temperature decreased below 16 °C. Both cycloheximide and actinomycin D inhibited the fragmentation in a dose-dependent manner, indicating that the transcription and protein synthesis took a part in the fragmentation. The tested strains with a high chemoreception sensitivity exhibited fragmentation similar to that of the strain with low sensitivity, but the transition temperature was lower. The biological significance of the fragmentation and its relationship with the other morphogenetic processes are discussed.
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References
Alexopoulos CJ (1998) Morphology and laboratory cultivation ofEchinostelium minutum. Am J Bot 47: 37–43
—, Mims CW (1979) Introductory mycology, 3rd edn. Wiley, New York
Ashworth JM, Dee J (1975) The biology of slime moulds. Arnold, London
Bailey J (1995) Plasmodial development in the myxomycetePhysarum polycephalum: genetic control and cellular events. Microbiology 141: 2355–2365
Carlile MJ, Watkinson SC (1994) The fungi. Academic Press, London
Chet I, Rusch HP (1969) Induction of spherule formation inPhysarum polycephalum by polyols. J Bacteriol 100: 673–678
Dove WF, Rusch HP (eds) (1980) Growth and differentiation inPhysarum polycephalum. Princeton University Press, Princeton
Goodman EM, Beck T (1974) Metabolism during differentiation in the slime moldPhysarum polycephalum. Can J Microbiol 20: 107–111
Gray WD, Alexopoulos CJ (1968) Biology of the Myxomycetes. Ronald Press, New York
Haskins EF (1968) Developmental studies on the true slime moldEchinostelium minutum. Can J Microbiol 14: 1309–1315
Heads RJ, Carpenter BG (1990) Differential synthesis of histone H1 during early spherulation inPhysarum polycephalum. Biochim Biophys Acta 1053: 56–62
Hüttermann A (1973) Biochemical events during spherule formation ofPhysarum polycephalum. Ber Deutsch Bot Ges 86: 55–76
— (1982) Enzyme and protein synthesis during differentiation ofPhysarum polycephalum. In: Aldrich HC, Daniel JW (eds) Cell biology ofPhysarum andDidymium, vol 2. Academic Press, New York, pp 77–99
Ishigam M, Kuroda K, Hatano S (1987) Dynamic aspects of the contractile system inPhysarum plasmodium III: cyclic contraction-relaxation of the plasmodial fragment in accordance with the generation—degeneration of cytoplasmic actomyosin fibrils. J Cell Biol 105: 381–386
Koya S, Ueda T (1998) The onset of rhythmic streaming in thePhysarum plasmodium: cooperative hierarchic organization of a multi-nucleate cell. ACH Models Chem 135: 297–304
Loidl P, Grobner P (1986) Biosynthesis and posttranslational acetylation of histones during spherulation ofPhysarum polycephalum. Nucleic Acid Res 14: 3745–3762
Raub TJ, Aldrich HC (1982) Sporangia, spherules and microcysts. In: Aldrich HC, Daniel JW (eds) Cell biology ofPhysarum andDidymium, vol 2. Academic Press, New York, pp 21–75
Rundquist A, Gott JM (1995) RNA editing of thecol mRNA throughout the life cycle ofPhysarum polycephalum. Mol Gen Genet 247: 306–311
Sauer H (1982) Developmental biology ofPhysarum. Cambridge University Press, Cambridge
Saunders DS (1978) An introduction to biological rhythms. Blackies and Sons, Bishopbriggs
Schreckenbach T, Walckhoff B, Verfuerth C (1981) Blue-light receptor in a white mutant ofPhysarum polycephalum mediates inhibition of spherulation and regulation of glucose metabolism. Proc Natl Acad Sci USA 78: 1009–1013
Starostzik C, Marwan W (1995) Functional mapping of the branched signal transduction pathway that controls sporulation inPhysarum polycephalum. Photochem Photobiol 62: 930–933
Ueda T (1996) Photobehavior and photomorphogenesis in the true slime moldPhysarum polycephalum. In: NIBB International Symposium on new prospects of photobiology, Okazaki, Japan, November 12–14, 1996, Session II-6
—, Carlile MJ (1983) The genetic basis of differences in cation chemoreception sensitivity in plasmodia of the myxomycetePhysarum polycephalum. J Gen Microbiol 129: 2475–2480
—, Kobatake Y (1978) Discontinuous changes in membrane activities of plasmodium ofPhysarum polycephalum caused by temperature variation: Effects on chemoreception and amoeboid motility. Cell Struct Funct 3: 129–139
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Kakiuchi, Y., Ueda, T. Fragmentation of the plasmodium into equally sized pieces by low temperatures in the true slime moldPhysarum polycephalum: A new morphogenesis. Protoplasma 206, 131–136 (1999). https://doi.org/10.1007/BF01279259
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DOI: https://doi.org/10.1007/BF01279259