Copper-transporting ATPases throughout the animal evolution - From clinics to basal neuron-less animals.

ATP7 genes, ATP7 proteins Animal models Copper-transporting ATPases Invertebrate Menkes disease Non-bilaterian Vertebrate Wilson’s disease

Journal

Gene
ISSN: 1879-0038
Titre abrégé: Gene
Pays: Netherlands
ID NLM: 7706761

Informations de publication

Date de publication:
15 Nov 2023
Historique:
received: 17 05 2023
revised: 01 08 2023
accepted: 16 08 2023
medline: 19 9 2023
pubmed: 20 8 2023
entrez: 19 8 2023
Statut: ppublish

Résumé

Copper-transporting ATPases are a group of heavy metal-transporting proteins and which can be found in all living organisms. In animals, they are generally referred to as ATP7 proteins and are involved in many different physiological processes including the maintaining of copper homeostasis and the supply of copper to cuproenzymes. A single ATP7 gene is present in non-chordate animals while it is divided into ATP7A and ATP7B in chordates. In humans, dysfunction of ATP7 proteins can lead to severe genetic disorders, such as, Menkes disease and Wilson's disease, which are characterized by abnormal copper transport and accumulation, causing significant health complications. Therefore, there is a substantial amount of research on ATP7 genes and ATP7 proteins in humans and mice to understand pathophysiological conditions and find potential therapeutic interventions. Copper-transporting ATPases have also been investigated in some non-mammalian vertebrates, protostomes, single-cellular eukaryotes, prokaryotes, and archaea to gain useful evolutionary insights. However, ATP7 function in many animals has been somewhat neglected, particularly in non-bilaterians. Previous reviews on this topic only broadly summarized the available information on the function and evolution of ATP7 genes and ATP7 proteins and included only the classic vertebrate and invertebrate models. Given this, and the fact that a considerable amount of new information on this topic has been published in recent years, the present study was undertaken to provide an up-to-date, comprehensive summary of ATP7s/ATP7s and give new insights into their evolutionary relationships. Additionally, this work provides a framework for studying these genes and proteins in non-bilaterians. As early branching animals, they are important to understand the evolution of function of these proteins and their important role in copper homeostasis and neurotransmission.

Identifiants

pubmed: 37597707
pii: S0378-1119(23)00561-9
doi: 10.1016/j.gene.2023.147720
pii:
doi:

Substances chimiques

Copper-Transporting ATPases EC 7.2.2.8
Copper 789U1901C5

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

147720

Informations de copyright

Copyright © 2023 The Author(s). Published by Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

István Fodor (I)

Ecophysiological and Environmental Toxicological Research Group, Balaton Limnological Research Institute, H-8237 Tihany, Hungary. Electronic address: fodor.istvan@blki.hu.

Luis Alfonso Yañez-Guerra (LA)

Living Systems Institute, University of Exeter, Stocker Road, Exeter, United Kingdom.

Bence Kiss (B)

Institute of Biochemistry and Medical Chemistry, Medical School, University of Pécs, H-7624 Pécs, Hungary.

Gergely Büki (G)

Department of Medical Genetics, Medical School, University of Pécs, H-7624 Pécs, Hungary.

Zsolt Pirger (Z)

Ecophysiological and Environmental Toxicological Research Group, Balaton Limnological Research Institute, H-8237 Tihany, Hungary.

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Classifications MeSH