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A combined proteomic and transcriptomic analysis of slime secreted by the southern bottletail squid, Sepiadarium austrinum (Cephalopoda).
Caruana, Nikeisha J; Cooke, Ira R; Faou, Pierre; Finn, Julian; Hall, Nathan E; Norman, Mark; Pineda, Sandy S; Strugnell, Jan M.
Afiliação
  • Caruana NJ; Department of Ecology, Environment and Evolution, School of Life Sciences, La Trobe University, Melbourne, Vic 3086, Australia. Electronic address: njcaruana@students.latrobe.edu.au.
  • Cooke IR; Department of Molecular and Cell Biology, James Cook University, Townsville, Qld 4811, Australia; Department of Biochemistry and Genetics, La Trobe Institute for Molecular Sciences, La Trobe University, Melbourne, Vic 3086, Australia.
  • Faou P; Department of Biochemistry and Genetics, La Trobe Institute for Molecular Sciences, La Trobe University, Melbourne, Vic 3086, Australia.
  • Finn J; Sciences, Museum Victoria, Carlton, Vic 3053, Australia.
  • Hall NE; Life Sciences Computation Centre, Victorian Life Sciences Computation Initiative, Carlton, Vic 3053, Australia.
  • Norman M; Sciences, Museum Victoria, Carlton, Vic 3053, Australia.
  • Pineda SS; Institute for Molecular Bioscience, The University of Queensland, QLD 4072, Australia.
  • Strugnell JM; Department of Ecology, Environment and Evolution, School of Life Sciences, La Trobe University, Melbourne, Vic 3086, Australia.
J Proteomics ; 148: 170-82, 2016 10 04.
Article em En | MEDLINE | ID: mdl-27476034
ABSTRACT
UNLABELLED Sepiadarium austrinum, the southern bottletail squid, is a small squid that inhabits soft sediments along Australia's south-east coast. When provoked, it rapidly secretes large volumes of slime, presumably as a form of chemical defense. We analyzed the proteomic composition of this slime using tandem mass spectrometry and transcriptomics and found that it was remarkably complex with 1735 identified protein groups (FDR0.01). To investigate the chemical defense hypothesis we performed an Artemia toxicity assay and used sequence analysis to search for toxin-like molecules. Although the slime did not appear to be toxic to Artemia we found 13 proteins in slime with the hallmarks of toxins, namely cysteine richness, short length, a signal peptide and/or homology to known toxins. These included three short (80-130AA) cysteine rich secreted proteins with no homology to proteins on the NCBI or UniProt databases. Other protein families found included, CAP, phospholipase-B, ShKT-like peptides, peptidase S10, Kunitz BPTI and DNase II. Quantitative analysis using intensity based absolute quantification (iBAQ via MaxQuant) revealed 20 highly abundant proteins, accounting for 67% of iBAQ signal, and three of these were toxin-like. No mucin homologues were found suggesting that the structure of the slime gel may be formed by an unknown mechanism. BIOLOGICAL

SIGNIFICANCE:

This study is the first known instance of a slime secretion from a cephalopod to be analyzed by proteomics methods and is the first investigation of a member of the family Sepiadariidae using proteomic methods. 1735 proteins were identified with 13 of these fitting criteria established for the identification of putative toxins. The slime is dominated by 20 highly abundant proteins with secreted, cysteine rich proteins. The study highlights the importance of 'omics approaches in understanding novel organisms.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Decapodiformes / Perfilação da Expressão Gênica / Proteômica Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Decapodiformes / Perfilação da Expressão Gênica / Proteômica Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2016 Tipo de documento: Article