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Gene Duplication and Spectral Diversification of Cone Visual Pigments of Zebrafish
Akito Chinena, Takanori Hamaokaa, Yukihiro Yamadaa, and Shoji Kawamuraaa Department of Integrated Biosciences, Graduate School of Frontier Sciences, The University of Tokyo, Chiba 277-8562, Japan
Corresponding author: Shoji Kawamura, Graduate School of Frontier Sciences, The University of Tokyo, Seimeitou #502, 5-1-5 Kashiwanoha, Kashiwa, Chiba 277-8562, Japan., kawamura{at}k.u-tokyo.ac.jp (E-mail)
Communicating editor: S. YOKOYAMA
max) of the reconstituted photopigments from the opsin cDNAs differed markedly among them: 558 nm (LWS-1), 548 nm (LWS-2), 467 nm (RH2-1), 476 nm (RH2-2), 488 nm (RH2-3), 505 nm (RH2-4), 355 nm (SWS1), 416 nm (SWS2), and 501 nm (RH1, rod opsin). The quantitative RT-PCR revealed a considerable difference among the opsin genes in the expression level in the retina. The expression of the two red opsin genes and of three green opsin genes, RH2-1, RH2-3, and RH2-4, is significantly lower than that of RH2-2, SWS1, and SWS2. These findings must contribute to our comprehensive understanding of visual capabilities of zebrafish and the evolution of the fish visual system and should become a basis of further studies on expression and developmental regulation of the opsin genes.
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