Evolution of the nitric oxide synthase family in vertebrates and novel insights in gill development

Author:

Annona Giovanni1ORCID,Sato Iori2ORCID,Pascual-Anaya Juan345ORCID,Osca David6ORCID,Braasch Ingo7ORCID,Voss Randal8,Stundl Jan91011ORCID,Soukup Vladimir9ORCID,Ferrara Allyse12,Fontenot Quenton12,Kuratani Shigeru23ORCID,Postlethwait John H.13,D'Aniello Salvatore1ORCID

Affiliation:

1. Biology and Evolution of Marine Organisms, Stazione Zoologica Anton Dohrn, Napoli 80121, Italy

2. Laboratory for Evolutionary Morphology, RIKEN Center for Biosystems Dynamics Research (BDR), Kobe 650-0047, Japan

3. Evolutionary Morphology Laboratory, RIKEN Cluster for Pioneering Research (CPR), Chuo-ku, Kobe, Hyogo 650-0047, Japan

4. Department of Animal Biology, Faculty of Sciences, University of Málaga, Spain

5. Andalusian Centre for Nanomedicine and Biotechnology (BIONAND), Málaga, Spain

6. Faculty of Marine Sciences, University Institute of Environmental Studies and Natural Resources (IUNAT), University of Las Palmas de Gran Canaria, Canary Islands, Spain

7. Department of Integrative Biology and Program in Ecology, Evolution and Behavior (EEB), Michigan State University, East Lansing, MI 48824, USA

8. Department of Neuroscience, Spinal Cord and Brain Injury Research Center, and Ambystoma Genetic Stock Center, University of Kentucky, Lexington, KY, USA

9. Department of Zoology, Faculty of Science, Charles University, Prague, Czech Republic

10. Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA

11. South Bohemian Research Center of Aquaculture and Biodiversity of Hydrocenoses, Faculty of Fisheries and Protection of Waters, University of South Bohemia in Ceske Budejovice, Vodnany, Czech Republic

12. Department of Biological Sciences, Nicholls State University, Thibodaux, LA 70301, USA

13. Institute of Neuroscience, University of Oregon, Eugene, OR 97403, USA

Abstract

Nitric oxide (NO) is an ancestral key signalling molecule essential for life and has enormous versatility in biological systems, including cardiovascular homeostasis, neurotransmission and immunity. Although our knowledge of NO synthases (Nos), the enzymes that synthesize NO in vivo , is substantial, the origin of a large and diversified repertoire of nos gene orthologues in fishes with respect to tetrapods remains a puzzle. The recent identification of nos3 in the ray-finned fish spotted gar, which was considered lost in this lineage, changed this perspective. This finding prompted us to explore nos gene evolution, surveying vertebrate species representing key evolutionary nodes. This study provides noteworthy findings: first, nos2 experienced several lineage-specific gene duplications and losses. Second, nos3 was found to be lost independently in two different teleost lineages, Elopomorpha and Clupeocephala. Third, the expression of at least one nos paralogue in the gills of developing shark, bichir, sturgeon, and gar, but not in lamprey, suggests that nos expression in this organ may have arisen in the last common ancestor of gnathostomes. These results provide a framework for continuing research on nos genes’ roles, highlighting subfunctionalization and reciprocal loss of function that occurred in different lineages during vertebrate genome duplications.

Publisher

The Royal Society

Subject

General Agricultural and Biological Sciences,General Environmental Science,General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine

Reference58 articles.

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