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Expression Analysis of Visual Arrestin gene during Ocular Development of Olive Flounder (Paralichthys olivaceus)

  • Received : 2013.08.25
  • Accepted : 2013.09.07
  • Published : 2013.09.30

Abstract

Olive flounder (Paralichthys olivaceus) is one of the commercial important flatfish species in Korea. The ocular signal transduction pathway is important in newly hatched flounders because it is closely involved in the initial feeding phase thus essential for survival during the juvenile period. However, the study of gene expression during ocular development is incomplete in olive flounder. Therefore we examined the expression analysis of specifically induced genes during the development of the visual system in newly hatched flounders. We searched ocular development-involved gene in the database of expressed sequence tags (ESTs) from olive flounder eye and this gene similar to arrestin with a partial sequence homology. Microscopic observation of retinal formation corresponded with the time of expression of the arrestin gene in the developmental stage. These results suggest that arrestin plays a vital role in the visual signal transduction pathway of the retina during ocular development. The expression of arrestin was strong in the ocular system during the entirety of the development stages. Our findings regarding arrestin have important implications with respect to its biological role and evolution of G-protein coupled receptor (GPCR) signaling in olive flounder. Further studies are required on the GPCR-mediated signaling pathway and to decipher the functional role of arrestin.

Keywords

References

  1. Attramadal H, Arriza JL, Aoki C, Dawson TM, Codina J, Kwatra MM, Snyder SH, Caron MG, Lefkowitz RJ (1992) Beta-arrestin2, a novel member of the arrestin/beta-arrestin gene family. J Biol Chem 267:17882-17890.
  2. Bohn LM, Lefkowitz RJ, Gainetdinov RR, Peppel K, Caron MG, Lin FT (1999) Enhanced morphine analgesia in mice lacking beta-arrestin 2. Science 286:2495-2498. https://doi.org/10.1126/science.286.5449.2495
  3. Burns ME, Arshavsky VY (2005) Beyond counting photons: trials and trends in vertebrate visual transduction. Neuron 48:387-401. https://doi.org/10.1016/j.neuron.2005.10.014
  4. Conner DA, Mathier MA, Mortensen RM, Christe M, Vatner SF, Seidman CE, Seidman JG (1997) beta-Arrestin1 knockout mice appear normal but demonstrate altered cardiac responses to beta-adrenergic stimulation. Circ Res 81:1021-1026. https://doi.org/10.1161/01.RES.81.6.1021
  5. Cook A (1996) Ontogeny of feeding morphology and kinematics in juvenile fishes: a case study of the cottid fish Clinocottus analis. J Exp Biol 199:1961-1971.
  6. Craft CM, Whitmore DH, Wiechmann AF (1994) Cone arrestin identified by targeting expression of a functional family. J Biol Chem 269:4613-4619.
  7. Easter SS Jr, Nicola GN (1996) The development of vision in the zebrafish (Danio rerio). Dev Biol 180:646-663. https://doi.org/10.1006/dbio.1996.0335
  8. Ferguson SS (2001) Evolving concepts in G proteincoupled receptor endocytosis: the role in receptor desensitization and signaling. Pharmacol Rev 53:1-24.
  9. Ferguson SS, Downey WE 3rd, Colapietro AM, Barak LS, Menard L, Caron MG (1996) Role of beta-arrestin in mediating agonist-promoted G protein-coupled receptor internalization. Science 271:363-366. https://doi.org/10.1126/science.271.5247.363
  10. Francis AW Jr, Turingan RG (2008) Morphological and biomechanical changes of the feeding apparatus in developing southern flounder, Paralichthys lethostigma. J Morphol 269:1169-1180. https://doi.org/10.1002/jmor.10631
  11. Freedman NJ, Lefkowitz RJ (1996) Desensitization of G protein-coupled receptors. Recent Prog Horm Res 51:319-351.
  12. Fu Y, Yau KW (2007) Phototransduction in mouse rods and cones. Pflugers Arch 454:805-819. https://doi.org/10.1007/s00424-006-0194-y
  13. Gibb A (1995) Kinematics of prey capture in a flatfish, Pleuronichthys verticalis. J Exp Biol 198:1173-1183.
  14. Goodman OB Jr, Krupnick JG, Santini F, Gurevich VV, Penn RB, Gagnon AW, Keen JH, Benovic JL (1996) Beta-arrestin acts as a clathrin adaptor in endocytosis of the beta2-adrenergic receptor. Nature 383:447-450. https://doi.org/10.1038/383447a0
  15. Gurevich VV (1998) The selectivity of visual arrestin for light-activated phosphorhodopsin is controlled by multiple nonredundant mechanisms. J Biol Chem 273:15501-15506. https://doi.org/10.1074/jbc.273.25.15501
  16. Kawamura S, Tachibanaki S (2008) Rod and cone photoreceptors: molecular basis of the difference in their physiology. Comp Biochem Physiol A Mol Integr Physiol 150:369-377. https://doi.org/10.1016/j.cbpa.2008.04.600
  17. Krupnick JG, Gurevich VV, Benovic JL (1997) Mechanism of quenching of phototransduction. Binding competition between arrestin and transducin for phosphorhodopsin. J Biol Chem 272:18125-18131. https://doi.org/10.1074/jbc.272.29.18125
  18. Lamb TD, Pugh EN Jr (2006) Phototransduction, dark adaptation, and rhodopsin regeneration the proctor lecture. Invest Ophthalmol Vis Sci 47:5137-5152. https://doi.org/10.1167/iovs.06-0187
  19. Lee JH, Noh JK, Kim HC, Park CJ, Min BH, Kim YO (2009) EST-based identification of genes expressed in the brain of the olive flounder Paralichthys olivaceus Fish Aqua Sci 12:286-292.
  20. Lee JH, Noh JK, Kim HC, Park CJ, Min BH, Ha SJ (2010) Molecular characterization of the ocular EST clones from olive flounder, Paralichthys olivaceus. Dev Reprod 14:107-113.
  21. Liem KF, Wallace JW, Whalen G (1985) Flatfishes breathe symmetrically: an experimental reappraisal. Exp Biol 44:159-172.
  22. Lohse MJ, Benovic JL, Codina J, Caron MG, Lefkowitz RJ (1990) Beta-Arrestin: a protein that regulates betaadrenergic receptor function. Science 248:1547-1550. https://doi.org/10.1126/science.2163110
  23. Luttrell LM, Lefkowitz RJ (2002) The role of betaarrestins in the termination and transduction of Gprotein-coupled receptor signals. J Cell Sci 115:455-465.
  24. Martinez GM, Bolker JA (2003) Embryonic and larval staging of summer flounder (Paralichthys dentatus). J Morphol 255:162-176. https://doi.org/10.1002/jmor.10053
  25. Miwa S, Inui Y (1987) Effects of various doses of thyroxine and triiodothyronine on the metamorphosis of flounder (Paralichthys olivaceus). Gen Comp Endocrinol 67:356-363. https://doi.org/10.1016/0016-6480(87)90190-0
  26. Miwa S, Tagawa M, Inui Y, Hirano T (1988) Thyroxine surge in metamorphosing flounder larvae. Gen Comp Endocrinol 70:158-163. https://doi.org/10.1016/0016-6480(88)90105-0
  27. Murakami A, Yajima T, Sakuma H, McLaren MJ, Inana G (1993) X-arrestin: a new retinal arrestin mapping to the X chromosome. FEBS Lett 334:203-209. https://doi.org/10.1016/0014-5793(93)81712-9
  28. Rahmann H, Jeserich G, Zeutzius I (1979) Ontogeny of visual acuity of rainbow trout under normal conditions and light deprivation. Behaviour 68:315-322. https://doi.org/10.1163/156853979X00359
  29. Roman G, He J, Davis RL (2000) Kurtz, a novel nonvisual arrestin, is an essential neural gene in Drosophila. Genetics 155:1281-1295.
  30. Schmitt E, Kunz YW (1989) Retinal morphogenesis in the rainbow trout, Salmo gairdneri. Brain Behav Evol 34:48-64. https://doi.org/10.1159/000116491
  31. Shand J, Doving KB, Collin SP (1999) Optics of the developing fish eye: comparisons of Matthiessen's ratio and the focal length of the lens in the black bream Acanthopagrus butcheri (Sparidae, Teleostei). Vision Res 39:1071-1078. https://doi.org/10.1016/S0042-6989(98)00215-6
  32. Shinohara T, Dietzschold B, Craft CM, Wistow G, Early JJ, Donoso LA, Horwitz J, Tao R (1987) Primary and secondary structure of bovine retinal S antigen (48-kDa protein). Proc Natl Acad Sci USA 84:6975-6979. https://doi.org/10.1073/pnas.84.20.6975
  33. Wilden U, Hall SW, Kuhn H (1986) Phosphodiesterase activation by photoexcited rhodopsin is quenched when rhodopsin is phosphorylated and binds the intrinsic 48-kDa protein of rod outer segments. Proc Natl Acad Sci USA 83:1174-1178. https://doi.org/10.1073/pnas.83.5.1174
  34. Yamaki K, Takahashi Y, Sakuragi S, Matsubara K (1987) Molecular cloning of the S-antigen cDNA from bovine retina. Biochem Biophys Res Commun 14:904-910.
  35. Yamano K, Miwa S (1998) Differential gene expression of thyroid hormone receptor alpha and beta in fish development. Gen Comp Endocrinol 109:75-85. https://doi.org/10.1006/gcen.1997.7011
  36. Yamano K, Miwa S, Obinata T, Inui Y (1991) Thyroid hormone regulates developmental changes in muscle during flounder metamorphosis. Gen Comp Endocrinol 81:464-472. https://doi.org/10.1016/0016-6480(91)90174-5
  37. Yamano K, Takano-Ohmuro H, Obinata T, Inui Y (1994) Effect of thyroid hormone on developmental transition of myosin light chains during flounder metamorphosis. Gen Comp Endocrinol 93:321-326. https://doi.org/10.1006/gcen.1994.1036
  38. Yue R, Kang J, Zhao C, Hu W, Tang Y, Liu X, Pei G (2009). Beta-arrestin1 regulates zebrafish hematopoiesis through binding to YY1 and relieving polycomb group repression. Cell 139:535-546. https://doi.org/10.1016/j.cell.2009.08.038