Modularity in protein evolution: modular organization and de novo domain evolution in mollusc metallothionein

Metallothioneins (MTs) are proteins devoted to the control of metal homeostasis and detoxification, and therefore, MTs have been crucial for the adaptation of the living beings to variable situations of metal bioavailability. The evolution of MTs is, however, not yet fully understood, and to provide...

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Detalles Bibliográficos
Autores: Calatayud, Sara, Garcia-Risco, Mario, Pedrini-Martha, Veronika, Eernisse, Douglas J., Dallinger, Reinhard, Palacios Bonilla, Òscar, Capdevila Vidal, Mercè, Albalat Rodríguez, Ricard
Tipo de recurso: artículo
Estado:Versión aceptada para publicación
Fecha de publicación:2020
País:España
Institución:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
Repositorio:Recercat. Dipósit de la Recerca de Catalunya
OAI Identifier:oai:recercat.cat:2445/173669
Acceso en línea:https://hdl.handle.net/2445/173669
Access Level:acceso abierto
Palabra clave:Mol·luscs
Evolució (Biologia)
Proteïnes
Mollusks
Evolution (Biology)
Proteins
Descripción
Sumario:Metallothioneins (MTs) are proteins devoted to the control of metal homeostasis and detoxification, and therefore, MTs have been crucial for the adaptation of the living beings to variable situations of metal bioavailability. The evolution of MTs is, however, not yet fully understood, and to provide new insights into it, we have investigated the MTs in the diverse classes of Mollusks. We have shown that most molluskan MTs are bimodular proteins that combine six domains α, β1, β2, β3, γ, and δ in a lineage-specific manner. We have functionally characterized the Neritimorpha β3β1 and the Patellogastropoda γβ1 MTs, demonstrating the metal-binding capacity of the new γ domain. Our results have revealed a modular organization of mollusk MT, whose evolution has been impacted by duplication, loss, and de novo emergence of domains. MTs represent a paradigmatic example of modular evolution probably driven by the structural and functional requirements of metal binding.