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The Globin Gene Family in Arthropods: Evolution and Functional Diversity
Indexado
WoS WOS:000566232200001
Scopus SCOPUS_ID:85090003815
DOI 10.3389/FGENE.2020.00858
Año 2020
Tipo artículo de investigación

Citas Totales

Autores Afiliación Chile

Instituciones Chile

% Participación
Internacional

Autores
Afiliación Extranjera

Instituciones
Extranjeras


Abstract



Globins are small heme-proteins that reversibly bind oxygen. Their most prominent roles in vertebrates are the transport and storage of O(2)for oxidative energy metabolism, but recent research has suggested alternative, non-respiratory globin functions. In the species-rich and ecologically highly diverse taxon of arthropods, the copper-containing hemocyanin is considered the main respiratory protein. However, recent studies have suggested the presence of globin genes and their proteins in arthropod taxa, including model species like Drosophila. To systematically assess the taxonomic distribution, evolution and diversity of globins in arthropods, we systematically searched transcriptome and genome sequence data and found a conserved, widespread occurrence of three globin classes in arthropods: hemoglobin-like (HbL), globin X (GbX), and globin X-like (GbXL) protein lineages. These globin types were previously identified in protostome and deuterostome animals including vertebrates, suggesting their early ancestry in Metazoa. TheHbLgenes show multiple, lineage-specific gene duplications in all major arthropod clades. SomeHbLgenes (e.g.,Glob2and3ofDrosophila) display particularly fast substitution rates, possibly indicating the evolution of novel functions, e.g., in spermatogenesis. In contrast, arthropodGbXandGbXLglobin genes show high evolutionary stability: GbXL is represented by a single-copy gene in all arthropod groups except Brachycera, and representatives of the GbX clade are present in all examined taxa except holometabolan insects. GbX and GbXL both show a brain-specific expression. Most arthropod GbX and GbXL proteins, but also some HbL variants, include sequence motifs indicative of potential N-terminal acylation (i.e., N-myristoylation, 3C-palmitoylation). All arthropods except for the brachyceran Diptera harbor at least one such potentially acylated globin copy, confirming the hypothesis of an essential, conserved globin function associated with the cell membrane. In contrast to other animals, the fourth ancient globin lineage, represented by neuroglobin, appears to be absent in arthropods, and the putative arthropod orthologs of the fifth metazoan globin lineage, androglobin, lack a recognizable globin domain. Thus, the remarkable evolutionary stability of some globin variants is contrasted by occasional dynamic gene multiplication or even loss of otherwise strongly conserved globin lineages in arthropod phylogeny.

Revista



Revista ISSN
Frontiers In Genetics 1664-8021

Métricas Externas



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Disciplinas de Investigación



WOS
Genetics & Heredity
Scopus
Genetics
Genetics (Clinical)
Molecular Medicine
SciELO
Sin Disciplinas

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Publicaciones WoS (Ediciones: ISSHP, ISTP, AHCI, SSCI, SCI), Scopus, SciELO Chile.

Colaboración Institucional



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Autores - Afiliación



Ord. Autor Género Institución - País
1 Prothmann, Andreas Hombre Johannes Gutenberg Univ Mainz - Alemania
Johannes Gutenberg Universität Mainz - Alemania
Johannes Gutenberg-Universität Mainz - Alemania
2 Hoffmann, Federico G. Hombre Mississippi State Univ - Estados Unidos
College of Agriculture and Life Sciences - Estados Unidos
Mississippi State University - Estados Unidos
3 OPAZO-CARVALLO, JUAN CRISTOBAL Hombre Universidad Austral de Chile - Chile
Núcleo Milenio de Enfermedades asociadas a Canales Iónicos - Chile
4 Herbener, Peter Hombre Johannes Gutenberg Univ Mainz - Alemania
Johannes Gutenberg Universität Mainz - Alemania
Johannes Gutenberg-Universität Mainz - Alemania
5 Storz, Jay F. Hombre Univ Nebraska - Estados Unidos
School of Biological Sciences - Estados Unidos
6 Burmester, Thorsten Hombre UNIV HAMBURG - Alemania
Universität Hamburg - Alemania
7 Hankeln, Thomas Hombre Johannes Gutenberg Univ Mainz - Alemania
Johannes Gutenberg Universität Mainz - Alemania
Johannes Gutenberg-Universität Mainz - Alemania

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Financiamiento



Fuente
National Science Foundation
Fondo Nacional de Desarrollo Científico y Tecnológico (FONDECYT)
Ministerio de Economía, Fomento y Turismo
Fondo Nacional de Desarrollo Científico y Tecnológico
Iniciativa Científica Milenio
National Institutes of Health
Ministerio de Economía, Fomento y Turismo, Chile
Deutsche Forschungsgemeinschaft
DFG
Fondo Nacional de Desarrollo Científico, Tecnológico y de Innovación Tecnológica
Fondo Nacional de Desarrollo Científico y Tecnológico
Fondo Nacional de Desarrollo Científico, Tecnológico y de Innovación Tecnológica
Millennium Nucleus of Ion Channels Associated Diseases (MiNICAD), Iniciativa Cientifica Milenio, Ministry of Economy, Development and Tourism, Chile
Ministerio de Economía, Fomento y Turismo
Johannes Gutenberg-Universität Mainz
Millennium Nucleus of Ion Channels Associated Diseases
Johannes Gutenberg University of Mainz
Johannes Gutenberg-Universität Mainz
Office of Integrative Activities; Office Of The Director

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Agradecimientos



Agradecimiento
TH acknowledged the support by an intramural "Stufe 1" grant from Johannes Gutenberg University of Mainz. The study emerged out of a project supported by DFG (Ha2103/5-2 and Bu956/6-3). FH work was partially funded by grant 1736026 from the National Science Foundation. JO work was partially funded by Fondo Nacional de Desarrollo Cientifico y Tecnologico (FONDECYT 1160627) and Millennium Nucleus of Ion Channels Associated Diseases (MiNICAD), Iniciativa Cientifica Milenio, Ministry of Economy, Development and Tourism, Chile. JS work was funded by grants from the National Institutes of Health (HL087216) and the National Science Foundation (OIA-1736249).
AP and TH wish to thank Dr. Hanno Schmidt and Mr. Matthias Weber (formerly Johannes Gutenberg University of Mainz) for their advice on RNA-Seq data analysis. Funding. TH acknowledged the support by an intramural “Stufe 1” grant from Johannes Gutenberg University of Mainz. The study emerged out of a project supported by DFG (Ha2103/5-2 and Bu956/6-3). FH work was partially funded by grant 1736026 from the National Science Foundation. JO work was partially funded by Fondo Nacional de Desarrollo Científico y Tecnológico (FONDECYT 1160627) and Millennium Nucleus of Ion Channels Associated Diseases (MiNICAD), Iniciativa Científica Milenio, Ministry of Economy, Development and Tourism, Chile. JS work was funded by grants from the National Institutes of Health (HL087216) and the National Science Foundation (OIA-1736249).

Muestra la fuente de financiamiento declarada en la publicación.