4.5 Article

The Transcriptome of the Zoanthid Protopalythoa variabilis (Cnidaria, Anthozoa) Predicts a Basal Repertoire of Toxin-like and Venom-Auxiliary Polypeptides

Journal

GENOME BIOLOGY AND EVOLUTION
Volume 8, Issue 9, Pages 3045-3064

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/gbe/evw204

Keywords

Zoanthidea; Hexacorallia; transcriptome; venomics; peptide toxin; RNA-seq; molecular toxinology

Funding

  1. Science and Technology Development Fund (FDCT) of Macau SAR [134/2014/A3, FDCT078/2011/A3, 069/2015/A2]
  2. Research Committee of University of Macau [MYRG2015-00214-ICMS-QRCM, MYRG2016-00133-ICMS-QRCM]
  3. Program on Toxinology
  4. Coordination for the Improvement of Higher Education Personnel (CAPES)
  5. Ministry of Education of the Federal Government of Brazil
  6. Brazilian National Council for Scientific and Technological Development, CNPq [408835/2013-3, 408934/2013-1]
  7. Ministry of Science, Technology and Innovation (MCTI)
  8. Brazilian National Council for Scientific and Technological Development (CNPq/MCTI-PROTAX)
  9. FACEPE [APQ-2012]

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Protopalythoa is a zoanthid that, together with thousands of predominantly marine species, such as hydra, jellyfish, and sea anemones, composes the oldest eumetazoan phylum, i.e., the Cnidaria. Some of these species, such as sea wasps and sea anemones, are highly venomous organisms that can produce deadly toxins for preying, for defense or for territorial disputes. Despite the fact that hundreds of organic and polypeptide toxins have been characterized from sea anemones and jellyfish, practically nothing is known about the toxin repertoire in zoanthids. Here, based on a transcriptome analysis of the zoanthid Protopalythoa variabilis, numerous predicted polypeptides with canonical venom protein features are identified. These polypeptides comprise putative proteins from different toxin families: neurotoxic peptides, hemostatic and hemorrhagic toxins, membrane-active (pore-forming) proteins, protease inhibitors, mixed-function venom enzymes, and venom auxiliary proteins. The synthesis and functional analysis of two of these predicted toxin products, one related to the ShK/Aurelin family and the other to a recently discovered anthozoan toxin, displayed potent in vivo neurotoxicity that impaired swimming in larval zebrafish. Altogether, the complex array of venom-related transcripts that are identified in P. variabilis, some of which are first reported in Cnidaria, provides novel insight into the toxin distribution among species and might contribute to the understanding of composition and evolution of venom polypeptides in toxiferous animals.

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