Acetabularia is a genus of green algae, specifically of the Polyphysaceae family, Typically found in subtropical waters, Acetabularia is a single-celled organism, but gigantic in size and complex in form, making it an excellent model organism for studying cell biology. In form, the mature Acetabularia resembles the round leaves of a nasturtium, is 0.5 to 10 cm tall and has three anatomical parts: a bottom rhizoid that resembles a set of short roots; a long stalk in the middle; and a top umbrella of branches that may fuse into a cap. The single nucleus of Acetabularia is located in the rhizoid, and allows the cell to regenerate completely if its cap is removed. The caps of two Acetabularia may also be exchanged, even from two different species. In addition, if a piece of the stem is removed, with no access to the nucleus in the rhizoid, this isolated stem piece will also grow a new cap.
In the 1930s–1950s Joachim Hämmerling conducted experiments in which he demonstrated Acetabularia's genetic information is contained in the nucleus. This was the first demonstration that genes are encoded by DNA in eukaryotes; earlier studies by Oswald Avery and others had shown that this was true for prokaryotes.
The name, Acetabularia, derives from the Latin word acetabulum, a broad, shallow cup used for dipping bread; the upturned cap of Acetabularia resembles such a cup. For this reason, it is also sometimes called mermaid's wineglass.
Anatomy and life cycle
Acetabularia has three basic parts: its rhizoid, a short set of root-like appendages that contain the nucleus and anchor the cell to fissures in a substrate; its median stalk, which accounts for most of its length; and its apex, where its cap forms. There are usually several whorls of hair-like appendages close to the apex.
Acetabularia are among the largest single-celled organisms, having also a remarkably large nucleus. During sexual reproduction, the nucleus undergoes multiple rounds of mitosis, forming many daughter nuclei all within one nuclear membrane. These nuclei undergo meiosis and are transported to the tips of the branches, the sporangia, where they are released as gametes.
Each Acetabularia cell is composed of three segments: the "foot" or base which contains the nucleus, the "stalk," and the "cap." Hämmerling exchanged caps between individuals from two species, A. mediterranea and A. crenulata. A. mediterranea has a smooth, disc shaped cap, while A. crenulata has a branched, flower-like cap.
After the exchange, each transplanted cap gradually changed from its original form to the form typical for the species of the base it was now attached to. This showed that the nucleus controlled the form of the cap.
In another experiment, Hämmerling inserted a nucleus from one species of Acetabularia into an intact Acetabularia of a different species. The Acetabularia then produced a hybrid cap with characteristics of both species. This showed that both nuclei influenced the form of the cap.
Hammerling's results showed that the nucleus of a cell contains the genetic information that directs cellular development.
Although a single cell, Acetabularia exhibits a remarkably complex shape and has therefore long been a model organism for studying gene expression and morphogenesis. It seems to transport messenger RNA molecules (in an inactive riboprotein form) from the nucleus to its apical tips, where they are translated into proteins. These molecules may be activated by proteolysis of their protein carrier molecules, but this has not been verified as yet.
Internal chemical gradients
In addition to its gradient in specific mRNA molecules, Acetabularia exhibits concentration gradients in several types of molecules, such as ascorbic acid.
Acetabularia has been used to study circadian rhythms.
Acetabularia species occasionally make their way into the aquarium trade. They are generally considered to be more difficult or unappealing macroalgae to care for in the reef aquarium, a fish-only, or a FOWLR (Fish Only With Live Rock) system, as they are delicate, readily eaten by herbivorous fish, grow slowly, and do not have the high nutrient uptake that reef aquarium refugium species (such as Chaetomorpha and Caulerpa) do. However, they are suitable for a macroalgae display tank, and thus macroalgae suppliers often carry species of Acetabularia.
- Lamouroux JVF (1812). "Extrait d'un mémoire sur la classification des Polypiers coralligènes non entièrement pierreux". Nouveaux Bulletin des Sciences, par la Société Philomathique de Paris 3: 181–188.
- Guiry, M.D. & Guiry, G.M. (2007). "Genus: Acetabularia taxonomy browser". AlgaeBase version 4.2 World-wide electronic publication, National University of Ireland, Galway. Retrieved 2007-09-27.
- Mandoli, DF (1998). "Elaboration of Body Plan and Phase Change during Development of Acetabularia: How Is the Complex Architecture of a Giant Unicell Built?". Annual Review of Plant Physiology and Plant Molecular Biology 49: 173–198. doi:10.1146/annurev.arplant.49.1.173. PMID 15012232.
- B. Goodwin (1994) "How the Leopard Changed its Spots" Weidenfeld & Nicolson, London
- Hämmerling, J (1953). "Nucleo-cytoplasmic relationships in the development of Acetabularia". J. Intern. Rev. Cytol. International Review of Cytology 2: 475–498. doi:10.1016/S0074-7696(08)61042-6. ISBN 978-0-12-364302-5.
- Lee, Robert E. (1999). Phycology. Cambridge, [England]: Cambridge University Press. p. 217. ISBN 978-0-521-63883-8.
- Shihira-Ishikawa, I (1984). "Chromosome behavior in the primary nucleus of Acetabularia calyculus as revealed by epifluorescent microscopy". Protoplasma 122: 27–34. doi:10.1007/BF01279434.
- Serio, D., Alongi, G., Catra, M., Cormaci, M. & Furnari, G. (2006). Changes in the benthic algal flora of Linosa Island (Straits of Sicily, Mediterranean Sea). Botanica Marina 49: 135–144.
- Berger, S. & Liddle. L.B. (2003). The life cycle of Acetabularia (Dasycladales, Chlorophyta): textbook accounts are wrong (Commentary). Phycologia 42(2): 204–207, 3 figs.
- Berger, S., Fettweiss, U., Gleissberg, S., Liddle, L.B., Richter, U., Sawitsky, H. & Zuccarello, G.C. (2003). 18S rDNA phylogeny and evaluation of cap development in Polyphysaceae (formerly Acetabulariaceae; Dasyladales, Chlorophyta). Phycologia 42: 506–561.
- Bonotto S (1994). "Developmental biology of Acetabularia". J. Mar. Biol. Ass. U.K. 74: 93–106. doi:10.1017/S0025315400035694.
- Berger S, de Groot E, Heuhaus G, Schweiger M (1987). "Acetabularia: a giant single cell organism with valuable advantages for cell biology". European Journal of Cell Biology 44: 349–370.
- Schweiger H? (1969). "Cell biology of Acetabularia". Current Topics in Microbiology and Immunology 50: 1–36.
- Cinelli, F. (1979). Acetabularia acetabulum (L.) Silva, Acetabularia parvula Solms-Laubach and Dasycladus vermicularis (Scopoli) Krasser (Chlorophyta, Dasycladales): ecology and distribution in the Mediterranean Sea.. In: Developmental Biology of Acetabularia. (Bonotto, S., Kefeli, V. & Puiseux-Dao, S. Eds), pp. 3–14. Amsterdam: Elsevier North Holland Biomedical Press.
- Cooper, J.J. & Mandoli, D.F. (1999). Physiological factors that aid differentiation of zygotes and early juveniles of Acetabularia acetabulum (Chlorophyta). Journal of Psychology 35: 143–151, 9 figs.
- Dazy, A. C., Borghi, H., Durand, M. & Puiseux-Dao, S. (1984). The effects of blue and red light on the transcellular electric potential, cytoplasmic streaming and rRNA transport in Acetabularia acetabulum. Proceedings of the International Seaweed Symposium 11: 193–197.
- Hunt, B.E. & Mandoli, D.F. (1996). A new, artificial seawater that facilitates growth of large numbers of cells of Acetabularia acetabulum (Chlorophyta) and reduces the labor inherent in cell culture. Journal of Psychology 32: 483–495, 6 figs, 3 tables.
- Kingsley, R.J., Van Gilder, R., LeGeros, R.Z. & Watabe, N. (2003). Multimineral calcareous deposits in the marine alga Acetabularia acetabulum (Chlorophyta; Dasycladaceae). Journal of Psychology 39: 937–947.
- Kratz, R.F., Young, P.A. & Mandoli, D.F. (1998). Timing and light regulation of apical morphogenesis during reproductive development in wild-type populations of Acetabularia acetabulum (Chlorophyceae). Journal of Psychology 34: 138–146, 6 figs, 2 tables.
- Lüttke, A. (1988). The lack of chloroplast DNA in Acetabularia mediterranea (acetabulum) (Chlorophyceae): A reinvestigation. Journal of Psychology 24: 173–180, 12 figs.
- Mandoli, D.F., Wexler, A., Teschmacher, J. & Zukowski, A. (1995). Note: Brief incubation of gametangia-bearing caps in antibiotics eliminates branching in progeny of Acetabularia acetabulum (Chlorophyta). Journal of Psychology 31: 844–848, 4 figs, 3 tables.
- Menzel, D. (1981). Development and fine structure of plugs in the cap rays of Acetabularia acetabulum (mediterranea) (L.) Silva (Dasycladales). Phycologia 20: 56–64, 21 figs.
- Nishimura, N.J. & Mandoli, D.F. (1992). Population analysis of reproductive cell structures of Acetabularia acetabulum (Chlorophyta). Phycologia 31: 351–358, 9 figs, 2 tables.
- Nishimura, N.J. & Mandoli, D.F. (1992). Vegetative growth of Acetabularia acetabulum (Chlorophyta): structural evidence for juvenile and adult phases in development. Journal of Psychology 28: 669–677, 7 figs.
- Zeller, A. & Mandoli, D.F. (1993). Growth of Acetabularia acetabulum (Dasycladales, Chlorophyta) on solid substrata at specific cell densities. Phycologia 32: 136–142