Two piranha parietopsins illuminate opsin diversification in teleosts
Abstract
Background: The teleost whole-genome duplication (TGD) contributed to functional diversification of opsins. Some TGD paralogs, including those of parapinopsin (PP), vertebrate ancient (VA) opsin, and long wavelength-sensitive opsin (LWS), show different absorption spectra and/or expression patterns. However, our knowledge of detailed evolutionary processes and mechanisms by which TGD contributed to opsin diversification is still limited.
Results: Here, we report that several characins, including the red piranha ( Pygocentrus nattereri ), have retained TGD paralogs of parietopsin (PT1 and PT2). While most teleosts, including zebrafish, have only PT1, the Mexican tetra ( Astyanax mexicanus ) and catfishes have only PT2. To assess the degree of functional diversification between PT1 and PT2, we characterized spectral properties, intracellular signaling properties, and expression patterns. Maximum absorption spectra differ slightly among PTs. Those of red piranha PT1, PT2, Mexican tetra PT2, and Japanese catfish ( Silurus asotus ) PT2 are located at 517 nm, 528 nm, 517 nm, and ~ 535 nm, respectively. In a heterologous cell-based assay, red piranha PT1 increased cellular cAMP in response to light, whereas PT2 decreased it, while neither induced a clear Ca ² ⁺ response under the conditions tested. Fluorescence in situ hybridization showed that (1) piranha PT1 and PT2 are expressed in the same pineal cells, and (2) they are also co-expressed with PP1 .
Conclusions: This study illustrates the importance of characterizing intracellular signaling properties to understand how TGD contributed to functional diversification of opsins.
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BibTeX
@article{sato2026piranha,
title = {{Two piranha parietopsins illuminate opsin diversification in teleosts}},
author = {Keita Sato and Takahiro Yamashita and Kazumi Sakai and Hideyo Ohuchi and Takehiro G. Kusakabe and Fuki Gyoja},
journal = {BMC Biology},
year = {2026},
month = oct,
doi = {10.1186/s12915-026-02759-5},
url = {https://link.springer.com/10.1186/s12915-026-02759-5},
note = {CC BY 4.0},
}
RIS
TY - JOUR
TI - Two piranha parietopsins illuminate opsin diversification in teleosts
AU - Keita Sato
AU - Takahiro Yamashita
AU - Kazumi Sakai
AU - Hideyo Ohuchi
AU - Takehiro G. Kusakabe
AU - Fuki Gyoja
PY - 2026
DA - 2026/10/07
JO - BMC Biology
DO - 10.1186/s12915-026-02759-5
UR - https://link.springer.com/10.1186/s12915-026-02759-5
AB - Background: The teleost whole-genome duplication (TGD) contributed to functional diversification of opsins. Some TGD paralogs, including those of parapinopsin (PP), vertebrate ancient (VA) opsin, and long wavelength-sensitive opsin (LWS), show different absorption spectra and/or expression patterns. However, our knowledge of detailed evolutionary processes and mechanisms by which TGD contributed to opsin diversification is still limited. Results: Here, we report that several characins, including the red piranha ( Pygocentrus nattereri ), have retained TGD paralogs of parietopsin (PT1 and PT2). While most teleosts, including zebrafish, have only PT1, the Mexican tetra ( Astyanax mexicanus ) and catfishes have only PT2. To assess the degree of functional diversification between PT1 and PT2, we characterized spectral properties, intracellular signaling properties, and expression patterns. Maximum absorption spectra differ slightly among PTs. Those of red piranha PT1, PT2, Mexican tetra PT2, and Japanese catfish ( Silurus asotus ) PT2 are located at 517 nm, 528 nm, 517 nm, and ~ 535 nm, respectively. In a heterologous cell-based assay, red piranha PT1 increased cellular cAMP in response to light, whereas PT2 decreased it, while neither induced a clear Ca ² ⁺ response under the conditions tested. Fluorescence in situ hybridization showed that (1) piranha PT1 and PT2 are expressed in the same pineal cells, and (2) they are also co-expressed with PP1 . Conclusions: This study illustrates the importance of characterizing intracellular signaling properties to understand how TGD contributed to functional diversification of opsins.
SN - 1741-7007
ER -