Cited by 855Coral and Marine Ecosystems StudiesMarine Invertebrate Physiology and EcologyGenomics and Phylogenetic Studies

Using the Acropora digitifera genome to understand coral responses to environmental change

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Shinzato, Chuya, Shoguchi, Eiichi, Kawashima, Takeshi, Hamada, Mayuko, Hisata, Kanako, Tanaka, Makiko, Fujie, Manabu, Fujiwara, Mayuki +5 more·2011·Nature

Abstract

Coral reefs are among the most biologically diverse ecosystems on the planet and are of great economic importance. They are under threat because the scleractinian corals at their core are susceptible to ocean acidification and rising seawater temperatures. The genome of the reef-building coral Acropora digitifera has been analysed with a view to understanding the molecular basis of symbiosis and responses to environmental change. The coral seems to have lost a key enzyme of cysteine biosynthesis, so may be dependent on its symbionts for this amino acid. It contains several genes with roles in protection from ultraviolet light that may have been acquired by horizontal transfer from prokaryotic organisms. The coral's innate immunity repertoire is more complex than that of the solitary sea anemone, suggesting that some of these genes are involved in symbiosis or coloniality. Despite the enormous ecological and economic importance of coral reefs, the keystone organisms in their establishment, the scleractinian corals, increasingly face a range of anthropogenic challenges including ocean acidification and seawater temperature rise1,2,3,4. To understand better the molecular mechanisms underlying coral biology, here we decoded the approximately 420-megabase genome of Acropora digitifera using next-generation sequencing technology. This genome contains approximately 23,700 gene models. Molecular phylogenetics indicate that the coral and the sea anemone Nematostella vectensis diverged approximately 500 million years ago, considerably earlier than the time over which modern corals are represented in the fossil record (∼240 million years ago)5. Despite the long evolutionary history of the endosymbiosis, no evidence was found for horizontal transfer of genes from symbiont to host. However, unlike several other corals, Acropora seems to lack an enzyme essential for cysteine biosynthesis, implying dependency of this coral on its symbionts for this amino acid. Corals inhabit environments where they are frequently exposed to high levels of solar radiation, and analysis of the Acropora genome data indicates that the coral host can independently carry out de novo synthesis of mycosporine-like amino acids, which are potent ultraviolet-protective compounds. In addition, the coral innate immunity repertoire is notably more complex than that of the sea anemone, indicating that some of these genes may have roles in symbiosis or coloniality. A number of genes with putative roles in calcification were identified, and several of these are restricted to corals. The coral genome provides a platform for understanding the molecular basis of symbiosis and responses to environmental changes.

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  • Much of the molecular architecture underlying neurogenesis and neuron functioning is conserved between bilaterians and cnidarians.

    “The publication of several cnidarian genomes has shown that much of the molecular architecture underlying neurogenesis and neuron functioning is conserved between bilaterians and cnidarians [17,47–51].”

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Authors
Shinzato, C., Shoguchi, E., Kawashima, T., Hamada, M., Hisata, K., Tanaka, M., Fujie, M., Fujiwara, M., Koyanagi, R., Ikuta, T., Fujiyama, A., Miller, D. J., & Satoh, N.
Affiliations
  • Okinawa Institute of Science and Technology Graduate University (JP)
  • National Institute of Genetics (JP)
  • ARC Centre of Excellence for Coral Reef Studies (AU)
Venue
Nature
Published
2011-07-24
Volume
476
Issue
7360
Pages
320-323
ISSN
  • 0028-0836 (ISSN-L)
  • 1476-4687
OpenAlex
W2171336109
Cited by
855
References
45
Citations by year
2026: 16 · 2025: 26 · 2024: 35 · 2023: 38 · 2022: 50 · 2021: 51 · 2020: 77 · 2019: 65 · 2018: 90 · 2017: 77 · 2016: 86 · 2015: 67 · 2014: 61 · 2013: 45 · 2012: 56
FWCI
49.03
Type
journal article
Language
en
Open access
Locations
  • Nature (publishedVersion, cc-by-nc-sa)
  • PubMed (publishedVersion)
  • ResearchOnline - JCU (James Cook University) (submittedVersion)
  • RePEc: Research Papers in Economics (submittedVersion)
Funders
  • Ministry of Education, Culture, Sports, Science and Technology
  • Okinawa Institute of Science and Technology Graduate University
  • University of the Ryukyus
  • Japan Society for the Promotion of Science (20121002)
Topics
  • Physical Sciences › Environmental Science › Ecology › Coral and Marine Ecosystems Studies
  • Physical Sciences › Earth and Planetary Sciences › Paleontology › Marine Invertebrate Physiology and Ecology
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Phylogenetic Studies
Keywords
Acropora digitifera, coral genome, cysteine biosynthesis, mycosporine-like amino acids, UV protection, horizontal gene transfer, innate immunity, Nematostella vectensis, ocean acidification, thermal stress (biology), coral reef degradation, coral evolution, gene loss
MeSH terms
Animals, Cyclohexylamines, Cystathionine beta-Synthase, Cysteine, DNA Damage, Fossils, Glycine, Molecular Sequence Data, Phylogeny, Sea Anemones, Symbiosis, Ultraviolet Rays, Genome, Protein Structure, Tertiary, Anthozoa, Climate Change, Coral Reefs

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