Proteomic Blueprint of Atlantic Cod (Gadus morhua) Otoliths Revealing Environmental Stress Insights through Label-Free Quantitative Shotgun Proteomics

Author:

Youssef Trevena N.1ORCID,Christian Sherri L.1,Rideout Rick2,Adamack Aaron2ORCID,Thibault Pierre34,Bonneil Eric5,Fridgen Travis D.6,Banoub Joseph126ORCID

Affiliation:

1. Biochemistry Department, Memorial University of Newfoundland, St. John’s, NL A1B 3X9, Canada

2. Fisheries and Oceans Canada, Northwest Atlantic Fisheries Centre, St. John’s, NL A1C 5X1, Canada

3. Department of Medicine, University of Montreal, Montreal, QC H3C 3J7, Canada

4. Institute for Research in Immunology and Cancer (IRIC), University of Montreal, Montreal, QC H3T 1J4, Canada

5. Department of Chemistry, University of Montreal, Montreal, QC H3A 0B8, Canada

6. Chemistry Department, Memorial University of Newfoundland, St. John’s, NL A1B 3X7, Canada

Abstract

Otoliths of the fish’s inner ear serve as a natural chronological recorder because of their continuous formation marked by daily, monthly, and annual increments. Despite their importance, the comprehensive protein content of otoliths remains not fully identified. Using the label-free shotgun proteomics method with one-dimensional liquid chromatography coupled to electrospray ionization-orbitrap tandem mass spectrometry, we quantified a broad range of proteins, with individual otoliths containing between 1341 and 1839 proteins. The identified proteins could potentially serve as a blueprint for fish growth from embryo to adult. We quantified eleven heat-shock proteins (HSPs) in both sexes and several proteins impacted by endocrine disruptors, indicating the otolith’s capacity to reflect environmental stress, potentially linked to climate change effects and altering of hormonal and neuroendocrine functions. Our bioinformatic ontology analysis confirmed the presence of proteins critical for various biological processes, including structural and enzymatic proteins. Protein–protein interaction (PPI) mapping also identified key interactions between the identified proteins. These findings significantly advance our understanding of otolith proteomics, offering a solid foundation for future work. Most of the identified proteins deposited daily and influenced by the environment were not implicated in the biomineralization of otolith, raising the potential for the otolith proteome to recreate details of fish life history at previously unrealized levels.

Publisher

MDPI AG

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