Eighteen Coral Genomes Reveal the Evolutionary Origin of <i>Acropora</i> Strategies to Accommodate Environmental Changes

Chuya Shinzato(The University of Tokyo), Konstantin Khalturin(Okinawa Institute of Science and Technology Graduate University), Jun Inoue(Okinawa Institute of Science and Technology Graduate University), Yuna Zayasu(Okinawa Institute of Science and Technology Graduate University), Miyuki Kanda(Okinawa Institute of Science and Technology Graduate University), Mayumi Kawamitsu(Okinawa Institute of Science and Technology Graduate University), Yuki Yoshioka(The University of Tokyo), Hiroshi Yamashita(Japan Fisheries Research and Education Agency), Go Suzuki(Japan Fisheries Research and Education Agency), Noriyuki Satoh(Okinawa Institute of Science and Technology Graduate University)
Molecular Biology and Evolution
September 1, 2020
Cited by 161Open Access
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Abstract

The genus Acropora comprises the most diverse and abundant scleractinian corals (Anthozoa, Cnidaria) in coral reefs, the most diverse marine ecosystems on Earth. However, the genetic basis for the success and wide distribution of Acropora are unknown. Here, we sequenced complete genomes of 15 Acropora species and 3 other acroporid taxa belonging to the genera Montipora and Astreopora to examine genomic novelties that explain their evolutionary success. We successfully obtained reasonable draft genomes of all 18 species. Molecular dating indicates that the Acropora ancestor survived warm periods without sea ice from the mid or late Cretaceous to the Early Eocene and that diversification of Acropora may have been enhanced by subsequent cooling periods. In general, the scleractinian gene repertoire is highly conserved; however, coral- or cnidarian-specific possible stress response genes are tandemly duplicated in Acropora. Enzymes that cleave dimethlysulfonioproprionate into dimethyl sulfide, which promotes cloud formation and combats greenhouse gasses, are the most duplicated genes in the Acropora ancestor. These may have been acquired by horizontal gene transfer from algal symbionts belonging to the family Symbiodiniaceae, or from coccolithophores, suggesting that although functions of this enzyme in Acropora are unclear, Acropora may have survived warmer marine environments in the past by enhancing cloud formation. In addition, possible antimicrobial peptides and symbiosis-related genes are under positive selection in Acropora, perhaps enabling adaptation to diverse environments. Our results suggest unique Acropora adaptations to ancient, warm marine environments and provide insights into its capacity to adjust to rising seawater temperatures.


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