Evidence map›Paper›PMID 41503633›Full record

ArticleGenome biology and evolution2026

Myriapod Metallothioneins Conserve the Ancestral Architecture of Arthropods While Displaying Lineage-Specific Adaptations in Metal Binding.

Òscar Palacios, Mercè Capdevila, Ricard Albalat

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Article in Genome biology and evolution, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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3 authors.

Òscar PalaciosDepartament de Química, Facultat de Ciències, Universitat Autònoma de Barcelona (UAB), Cerdanyola del Vallès, Spain.ORCID 0000-0002-2987-7303
Mercè CapdevilaDepartament de Química, Facultat de Ciències, Universitat Autònoma de Barcelona (UAB), Cerdanyola del Vallès, Spain.ORCID 0000-0002-2246-0994
Ricard AlbalatDepartament de Genètica, Microbiologia I Estadística, Facultat de Biologia, Universitat de Barcelona (UB), Barcelona, Spain.ORCID 0000-0003-0282-9595

Funding

ERDF/EU BIO2015-67358-C2-2-PGrup de Recerca de la Generalitat de Catalunya 2021SGR00372Grup de Recerca de la Generalitat de Catalunya 2021SGR00668Ministerio de Ciencia e Innovación
6 · The paper itself

Abstract

Metallothioneins (MTs) are central to metal metabolism and contribute to organismal adaptation to variable metal bioavailability across ecosystems. Although well studied in chordates and mollusks, MTs remain poorly investigated in many arthropod lineages, particularly within the Myriapoda subphylum. Myriapods, comprising thousands of millipede (Diplopoda) and centipede (Chilopoda) species, are especially relevant for evolutionary studies because they are the sister group to Pancrustacea (crustaceans and insects), and they are some of the earliest arthropods to colonize land. Their MTs therefore provide critical insights into the origin and evolution of arthropod MTs and into the molecular adaptations underlying the colonization of new environments. In this work, we have identified 48 putative MTs from 30 myriapod species, all classified as type 1 (MT1) and occurring in two configurations: the bidomain MT1S (S for short) or the multidomain MT1L (L for long) variants. Evolutionary analyses suggest that MT1S represents the ancestral type not only in myriapods but across Arthropoda, whereas MT1L likely arose during chilopod diversification, probably restricted to the order Glomerida. Despite shared structural features, metal-binding characterization of three myriapod MTs-GminMT1Sa, GminMT1La from Glomeridella minima, and LforMT1S from Lithobius forficatus-revealed marked functional differences. The diplopod proteins GminMT1Sa and GminMT1La displayed a Cd-thionein character, while the chilopod LforMT1S was a multipurpose protein, binding cadmium, zinc, and copper without a clear metal preference. These differences likely reflect distinct metal uptake, retention, and excretion strategies in diplopods and chilopods, associated with their ecological adaptations as peaceful decomposers and voracious predators, respectively.

Indexed as

Arthropod ProteinsArthropodsEvolution, MolecularMetallothioneinMetalsAdaptation, PhysiologicalAmino Acid SequenceAnimalsPhylogenyArthropod ProteinsMetallothioneinMetalsarthropoda MTsmetal-binding proteinsprotein domainsprotein modularity

Identifiers

PMID41503633
PMCPMC12800444

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