Literature DB >> 21172834

Reverse evolution in RH1 for adaptation of cichlids to water depth in Lake Tanganyika.

Haruka Nagai1, Yohey Terai, Tohru Sugawara, Hiroo Imai, Hidenori Nishihara, Michio Hori, Norihiro Okada.   

Abstract

Reverse evolution is a widespread phenomenon in biology, but the genetic mechanism for the reversal of a genetic change for adaptation to the ancestral state is not known. Here, we report the first case of complete reverse evolution of two amino acids, serine and alanine, at a single position in RH1 opsin pigment for adaptation to water depth. We determined RH1 sequences of cichlid fishes from four tribes of Lake Tanganyika with different habitat depths. Most of the species were divided into two types: RH1 with 292A for species in shallow water or 292S for species in deep water. Both types were adapted to their ambient light environments as indicated by the absorption spectra of the RH1 pigments. Based on the RH1 locus tree and ecological data, we inferred the ancestral amino acids at position 292 and the distribution of the depth ranges (shallow or deep) of ancestral species of each tribe. According to these estimates, we identified two distinct parallel adaptive evolutions: The replacement A292S occurred at least four times for adaptation from shallow to deep water, and the opposite replacement S292A occurred three times for adaptation from deep to shallow water. The latter parallelism represents the complete reverse evolution from the derived to the ancestral state, following back adaptive mutation with reversal of the RH1 pigment function accompanied by reversal of the species habitat shift.

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Year:  2010        PMID: 21172834     DOI: 10.1093/molbev/msq344

Source DB:  PubMed          Journal:  Mol Biol Evol        ISSN: 0737-4038            Impact factor:   16.240


  11 in total

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Review 3.  Proximate and ultimate causes of variable visual sensitivities: Insights from cichlid fish radiations.

Authors:  Karen L Carleton; Brian E Dalton; Daniel Escobar-Camacho; Sri Pratima Nandamuri
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4.  Group size adjustment to ecological demand in a cooperative breeder.

Authors:  Markus Zöttl; Joachim G Frommen; Michael Taborsky
Journal:  Proc Biol Sci       Date:  2013-02-06       Impact factor: 5.349

5.  Opsin evolution in damselfish: convergence, reversal, and parallel evolution across tuning sites.

Authors:  Christopher M Hofmann; N Justin Marshall; Kawther Abdilleh; Zil Patel; Ulrike E Siebeck; Karen L Carleton
Journal:  J Mol Evol       Date:  2012-10-19       Impact factor: 2.395

6.  Depth and substratum differentiations among coexisting herbivorous cichlids in Lake Tanganyika.

Authors:  Hiroki Hata; Haruki Ochi
Journal:  R Soc Open Sci       Date:  2016-11-16       Impact factor: 2.963

7.  Visual adaptation in Lake Victoria cichlid fishes: depth-related variation of color and scotopic opsins in species from sand/mud bottoms.

Authors:  Yohey Terai; Ryutaro Miyagi; Mitsuto Aibara; Shinji Mizoiri; Hiroo Imai; Takashi Okitsu; Akimori Wada; Shiho Takahashi-Kariyazono; Akie Sato; Herbert Tichy; Hillary D J Mrosso; Semvua I Mzighani; Norihiro Okada
Journal:  BMC Evol Biol       Date:  2017-08-22       Impact factor: 3.260

8.  Parallel evolution of gene expression between trophic specialists despite divergent genotypes and morphologies.

Authors:  Joseph A McGirr; Christopher H Martin
Journal:  Evol Lett       Date:  2018-02-14

9.  Plasticity of opsin gene expression in the adult red shiner (Cyprinella lutrensis) in response to turbid habitats.

Authors:  Chia-Hao Chang; Hong Young Yan
Journal:  PLoS One       Date:  2019-04-12       Impact factor: 3.240

10.  Visual adaptation of opsin genes to the aquatic environment in sea snakes.

Authors:  Takashi Seiko; Takushi Kishida; Mina Toyama; Takahiko Hariyama; Takashi Okitsu; Akimori Wada; Mamoru Toda; Yoko Satta; Yohey Terai
Journal:  BMC Evol Biol       Date:  2020-11-26       Impact factor: 3.260

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