| Literature DB >> 32526329 |
Elza Fonseca1, André M Machado2, Nair Vilas-Arrondo3, André Gomes-Dos-Santos1, Ana Veríssimo4, Pedro Esteves5, Tereza Almeida4, Gonçalo Themudo2, Raquel Ruivo2, Montse Pérez6, Rute da Fonseca7, Miguel M Santos1, Elsa Froufe2, Esther Román-Marcote6, Byrappa Venkatesh8, L Filipe C Castro9.
Abstract
Nuclear receptors (NRs) are key transcription factors that originated in the common ancestor of metazoans. The vast majority of NRs are triggered by binding to either endogenous (e.g. retinoic acid) or exogenous (e.g. xenobiotics) ligands, and their evolution and expansion is tightly linked to the function of endocrine systems. Importantly, they represent classic targets of physiological exploitation by endocrine disrupting chemicals. The NR gene repertoire in different lineages has been shaped by gene loss, duplication and mutation, denoting a dynamic evolutionary route. As the earliest diverging class of gnathostomes (jawed vertebrates), cartilaginous fishes offer an exceptional opportunity to address the early diversification of NR gene families and the evolution of the endocrine system in jawed vertebrates. Here we provide an exhaustive analysis into the NR gene composition in five elasmobranch (sharks and rays) and two holocephalan (chimaeras) species. For this purpose, we generated also a low coverage draft genome assembly of the chimaera small-eyed rabbitfish, Hydrolagus affinis. We show that cartilaginous fish retain an archetypal NR gene repertoire, similar to that of mammals and coincident with the two rounds of whole genome duplication that occurred in the gnathostome ancestor. Furthermore, novel gene members of the non-canonical NR0B receptors were found in the genomes of this lineage. Our findings provide an essential view into the early diversification of NRs in gnathostomes, paving the way for functional studies.Entities:
Keywords: Gene duplication; Gene loss; Genome; Nuclear receptors
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Year: 2020 PMID: 32526329 DOI: 10.1016/j.ygcen.2020.113527
Source DB: PubMed Journal: Gen Comp Endocrinol ISSN: 0016-6480 Impact factor: 2.822