Identificador persistente para citar o vincular este elemento: http://hdl.handle.net/10553/117846
Título: Evolution of the nitric oxide synthase family in vertebrates and novel insights in gill development
Autores/as: Annona, Giovanni
Sato, Iori
Pascual-Anaya, Juan
Osca Ferriol, David 
Braasch, Ingo
Voss, Randal
Stundl, Jan
Soukup, Vladimir
Ferrara, Allyse
Fontenot, Quenton
Kuratani, Shigeru
Postlethwait, John H.
D'Aniello, Salvatore
Clasificación UNESCO: 24 Ciencias de la vida
Palabras clave: Gene Duplication And Loss
Genome Duplication
Nos
Phylogenomics
Synteny, et al.
Fecha de publicación: 2022
Publicación seriada: Proceedings of the Royal Society B: Biological Sciences 
Resumen: 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.
URI: http://hdl.handle.net/10553/117846
ISSN: 0962-8452
DOI: 10.1098/rspb.2022.0667
Fuente: Proceedings of the Royal Society B: Biological Sciences [EISSN 1471-2954], v. 289 (1980), (Agosto 2022)
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