Developmental expression of S-antigen in fetal human and rat eye

References

• Wacker W. B., Donoso L A., Kalsow C M., Yankeelov J. A., Jr., Organisciak D. T. Experimental allergic uveitis. Isolation, characterization, and localization of a soluble uveitopathogenic antigen from bovine retina. J. Immunol. 1977; 119: 1949–1958
   PubMed Web of Science ®Google Scholar
• Kalsow C., Wacker W. B. Pineal reactivity of anti-retina sera. Invest. Ophthalmol. Vis. Sci. 1977; 16: 181–184
   PubMed Web of Science ®Google Scholar
• Kuhn H., Hall S. C., Wilden U. Light induced binding of 48-kDa protein to photoreceptor membranes is highly enhanced by phosphorylation of rhodopsin. FEBS Lett. 1984; 176: 473–478
   PubMed Web of Science ®Google Scholar
• Pfister C., Chabre M., Plouet J., Tuyen V. V., Dekozak Y., Faure J.-P., Kuhn H. Retinal S antigen identified as the 48K protein regulating light-dependent phosphodiesterase in rods. Science 1985; 228: 891–893
   PubMed Web of Science ®Google Scholar
• Zukerman R., Cheasty J. E. A 48 kDa protein arrests cGMP phosphodiesterase activation in retinal rod disk membrane. FEBS Lett. 1986; 207: 35–41
   PubMed Web of Science ®Google Scholar
• Faure J.-P. Autoimmunity and the retina. Curr. Topics Eye Res. 1980; 2: 215–302
   PubMedGoogle Scholar
• Gery I., Mochizuki M., Nussenblatt R. B. Retinal specific antigens and immunopathogenic processes they provoke. “Progress in retinal Research”, N. N. Obsborne, G. J. Chader. Pergamon Press, Oxford 1986; 75–109
   Google Scholar
• Dorey C., Faure J.-P. Isolement et characterisation partielle d'un antigene retinien responsable de l-uveo-rerinite autoimmune experimentale. Ann. Immunol. (Inst. Pasteur) 1977; 128: 229–232
   Google Scholar
• Wacker W. B. Retinal autoimmunity and the pathogenesis of uveitis. “Proc. Immunology of the Eye; Workshop II”, R. J. Helmsen, A. Suran, I. Gery, R. B. Nussenblatt. Information Retrieval, Washington, D.C 1981; 11–32
   Google Scholar
• Faure J.-P., Mirshani M., Dorey C., Thillaye B., De Kozak Y., Boucheix C. Production and specificity of monoclonal antibodies to retinal S- antigen. Curr. Eye Res. 1984; 2: 867–873
   Google Scholar
• Mirshahi M., Faure J.-P., Brisson P., Falcon J. L, Guerlotte J., Collin J. P. S-antigen immunoreactivity in retinal rods and cones and pineal photosensitive cells. Biol. Cell 1984; 52: 195–198
   PubMed Web of Science ®Google Scholar
• van Veen T., Elofsson R., Hartwig H. G., Gery I., Mochizuki M., Cena Y., Klein D. C. Retinal S-antigen: immunocytochemical and immunochemical studies on distribution in animal photoreceptors and pineal organs. Exp. Biol. 1986; 45: 15–25
   PubMedGoogle Scholar
• Tsuda M., Kikuchi T., Yamaki K., Shinohara T. The mouse S-antigen gene: comparison with human and Drosophila. Eur. J. Biol. 1991; 200: 95–101
   Google Scholar
• Yamaki K., Tsuda M., Shinohoara T. The sequence of human retinal S-antigen reveals similarities with a-transducin. FEBS Lett. 1988; 234: 39–43
   PubMed Web of Science ®Google Scholar
• Shinohara T., Dietzschold B., Craft C M., Wistow G., Early J. J., Donoso L A., Horwitz J., Tao R. Primary and secondary structure of bovine retinal S-antigen (48KDa protein). Proc. Natl. Acad. Sci. USA 1987; 86: 6975–6979
   Google Scholar
• Yamaki K., Takahashi Y., Sakuragi S., Matsubara K. Molecular cloning of the S-antigen cDNA from bovine retina. Biochem. Biophys. Res. Commun. 1987; 142: 904–910
   PubMed Web of Science ®Google Scholar
• Abe T., Yamaki K., Tsuda M., Singh V. K., Suzuki S., McKinnon R., Klein D. C., Donoso L A., Shinohara T. Rat pineal S-antigen: sequence analysis reveals presence of a-transducin homologous sequence. FEBS Lett. 1989; 247: 307–311
   PubMed Web of Science ®Google Scholar
• Tsuda M., Syed M., Bugra K., Whelan J. P., McGinnis J. F., Shinohara T. Structural analysis of mouse S-antigen. Gene 1988; Z3: 11–20
   Google Scholar
• Yamaki K., Tsuda M., Kikuchi T., Chen K-H., Huang K-P., Shinohara T. Structural organization of the human S-antigen gene. J Biol. Chem. 1990; 265: 20757–20762
   PubMed Web of Science ®Google Scholar
• Donoso L A., Merryman C. F., Edelberg K. E., Naids R., Kalsow C. S-antigen in the developing retina and pineal gland: A monoclonal antibody study. Invest. Ophthalmol. Vis. Sci. 1985; 26: 561–567
   PubMed Web of Science ®Google Scholar
• Hebel R., Stromberg M. W. Anatomy and Embryology of the Laboratory Rat. BioMed Verlag, Worthsee 1986; 231–252
   Google Scholar
• Hsu S. M., Raine L., Fanger H. The use of avidin-biotin-peroxidase complex (ABC) in immunoperoxidase technique: A comparison between ABC and unlabeled antibody (PAP) procedure. J. Histochem. Cytochem. 1981; 22: 577–580
   Google Scholar
• Young W. S., Ill, Bonner T. I., Brann M. R. Mesencephalic dopamine neurons regulate the expression of neuropeptide mRNAs in the rat forebrain. PNAS. 1986; S3: 9827–9831
   Google Scholar
• Young W. S., Ill, Mezey E., Siegel R. E. Vasopressin and oxytocin mRNAs in adrenalectomized and Brattleboro rats: analysis by quantitative in situ hybridization histochemistry. Mol. Brain Res. 1986; 1: 231–241
   Google Scholar
• Benovic J. L., Kuhn H., Weyand I., Codina J., Caron M. G., Lefkowitz R. J. Functional desensitization of the isolated 13-adrenergic receptor kinase: retinal protein arrestin (48-kDa protein). Proc. Natl. Acad. Sci. USA 1987; S4: 8879–8882
   Google Scholar
• Yamada T., Takeuchi Y., Komori N., Kobayashi H., Sakai Y., Hotta Y., Matsumoto H. A 49-kilodalton phosphoprotein in the Drosophila photoreceptor is an arrestin homolog. Science 1990; 248: 483–486
   PubMed Web of Science ®Google Scholar
• Bonting S. L., Caravaggio L L., Gouras P. The rhodopin cycle in the developing vertebrate retina. I Relation of rhodopin content, electroretinogram and rod structure in the rat. Exp. Eye Res. 1961; 1: 14–24
   PubMed Web of Science ®Google Scholar
• Nir I., Cohen D., Papermaster D. S. Immunocytochemical localization of opsin in the cell membrane of rat retinal photoreceptors. J. Cell Biol. 1984; 2S: 1788–1795
   Google Scholar
• Broekhuyse R. M., Kuhlmann E. D. Assay of S-antigen immunoreactivity in mammalian retinas in relation to age, ocular dimension and retinal degeneration. Jpn. J. Ophthalmol. 1989; 22: 243–250
   Google Scholar
• Mirshahi M., Borgese F., Razaghi A., Scheuring U., Garcia-Romeu F., Faure J.-P., Motais R. Immunological detection of arrestin, a phototransduction regulatory protein, in the cytosol of nucleated erythrocytes. FEBS Lett. 1989; 252: 240–243
   Google Scholar
• Faure J.-P., Mirshahi M. S-antigen in non ocular tissues. Curr. Eye Res. 1990; 9: 163–167, Suppl)
   PubMed Web of Science ®Google Scholar
• Breitman M. L., Tsuda M., Usukura J., Kikuchi T., Zucconi A., Shinohara T. Expression of S-antigen in retina, pineal gland, lens and brain is directed by 5′ flanking sequences. J. Biol. Chem. 1991; 266: 15505–15510
   PubMed Web of Science ®Google Scholar
• Lohse M. J., Benovic J. L., Codina J., Caron M. G., Lefkowitz R. J. 13-arrestin: a protein that regulates G-adrenergic receptor function. Science 1990; 242: 1547–1549
   Google Scholar
• Smith D. P., Shieh B-H., Zuker C. Isolation and structure of an arrestin gene from Drosophila. Neurobiology 1990; 87: 1003–1007
   Google Scholar
• Hyde D. R., Mecklenburg K. L., Pollack J., Vihtelic T. S., Benzer S. Twenty Drosophilia visual system cDNA clones: One is a homolog of human arrestin. Proc. Natl. Acad. Sci. USA 1990; 87: 1008–1012
   PubMed Web of Science ®Google Scholar