Synopsis
Unicellular organisms, such as related ciliates Blepharisma and Stentor, show a number of light-induced motile responses to spatial and temporal variations in the photic environment. Thanks to these photosensory capabilities, in unevenly lighted areas both species accumulate in places of optimal light intensity (photodispersal) most suitable for their growth, survival, and development. Both microorganisms lack clearly specified sense organs, as are found in multicellular organisms, however they bear conspicuous subpellicular granules (photoreceptive units) able to perceive the quantity and quality of light. The absorption of photons by cells is thereby converted to internal biophysical/biochemical signals, resulting in the modification of ciliary beating and hence the pattern of motile behavior. Blepharisma and Stentorhave been found quite suitable for the study of cellular photoreception employing different biophysical or biochemical experimental methods as well as...
References
Fabczak H (2000) Protozoa as model system for studies of sensory light transduction: photophobic response in the ciliate Stentor and Blepharisma. Acta Protozool 39:171–181
Fabczak H, Sobierajska K, Fabczak S (2008) A rhodopsin immunoanalog in the related photosensitive Blepharisma japonicum and Stentor coeruleus. Photochem Photobiol Sci 7:1041–1045
Ishida M, Shigenaka Y, Taneda K (1989) Studies on the mechanism of cell elongation in Blepharisma japonicum. I. Physiological mechanism how light stimulation evokes cell eleongation. Eur J Protistol 25:182–186
Krispel CM, Sokolov M, Chen YM, Song H, Herrmann R, Arshavsky VY, Burns ME (2007) Phosducin regulates the expression of transducin βγ-subunits in rod photoreceptors and does not contribute to phototransduction adaptation. J Gen Physiol 130:303–312
Marino MJ, Sherman TG, Wood DC (2001) Partial cloning of putative G-proteins modulating mechanotransduction in the ciliate Stentor. J Eukaryot Microbiol 48:527–536
Nakaoka Y, Tokioka R, Shinozawa T, Usukura J (1991) Photoreception of Paramecium cilia: localization of photosensitivity and binding with anti-frog-rhodopsin IgG. J Cell Sci 99:67–72
Podesta A, Marangoni R, Villani C, Colombetti G (2007) A rhodopsin-like molecule on the plasma membrane of Fabrea salina. J Eukaryot Microbiol 41:565–569
Schulz R (2001) The pharmacology of phosducin. Pharmacol Res 43:1–10
Sobierajska K, Fabczak H, Fabczak S (2006) Photosensory transduction in unicellular eukaryotes: a comparison between related ciliates Blepharisma japonicum and Stentor coeruleus and photoreceptor cells of higher organisms. J Photochem Photobiol B 83:163–171
Sobierajska K, Głos J, Daborowska J, Kucharska J, Bregier C, Fabczak S, Fabczak H (2010) Visualization of the interaction between Gβγ and tubulin during light-induced cell elongation of Blepharisma japonicum. Photochem Photobiol Sci 9:1101–1110
Sobierajska K, Joachimiak E, Bregier C, Fabczak S, Fabczak H (2011) Effect of phosducin silincing on the photokinetic motile response of Blepharisma japonicum. Photochem Photobiol Sci 9:19–24
Tao N, Deforce L, Romanowski M, Meza-Keuthen S, Song P-S, Furuja M (1994) Stentor and Blepharisma photoreceptors. Structure and function. Acta Protozool 33:199–211
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Fabczak, H., Fabczak, S. (2015). Signal Recognition in Lower Organisms: Light-Induced Control of Cell Movement in the Ciliates Blepharisma and Stentor . In: Wells, R., Bond, J., Klinman, J., Masters, B., Bell, E. (eds) Molecular Life Sciences. Springer, New York, NY. https://doi.org/10.1007/978-1-4614-6436-5_734-1
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DOI: https://doi.org/10.1007/978-1-4614-6436-5_734-1
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