Characterization of the turbot Scophthalmus maximus (L.) myeloperoxidase. An insight into the evolution of vertebrate peroxidases

dc.contributor.affiliationUniversidade de Santiago de Compostela. Departamento de Bioloxía Funcionalgl
dc.contributor.affiliationUniversidade de Santiago de Compostela. Departamento de Microbioloxía e Parasitoloxíagl
dc.contributor.affiliationUniversidade de Santiago de Compostela. Instituto de Acuiculturagl
dc.contributor.affiliationUniversidade de Santiago de Compostela. Instituto de Investigación e Análises Alimentariasgl
dc.contributor.authorNoia Guldrís, Manuel
dc.contributor.authorFontenla Iglesias, Francisco
dc.contributor.authorValle Cao, Alejandra
dc.contributor.authorBlanco Abad, Verónica
dc.contributor.authorLeiro Vidal, José Manuel
dc.contributor.authorLamas Fernández, Jesús
dc.date.accessioned2021-02-03T10:01:33Z
dc.date.available2022-01-04T02:00:09Z
dc.date.issued2021
dc.description.abstractWe have completed the characterization of the turbot (Scophthalmus maximus) myeloperoxidase (mpx) gene and protein, which we partially described in a previous study. The turbot mpx gene has 15 exons that encode a protein of 767 aa, with a signal peptide, propeptide and light and heavy chains, and also with haem cavities, a Ca+2-binding motif and several N- and O-glycosylation sites. The mature protein forms homodimers of about 150 kDa and is very abundant in turbot neutrophils. In addition to the mpx (epx2a) gene, another three peroxidase genes, named epx1, epx2b1 and epx2b2, were identified in the turbot genome. Epx1, Epx2b1 and Epx2b2 proteins also have signal peptides and many structural characteristics of mammalian MPO and eosinophil peroxidase (EPX). Mpx was strongly expressed in head kidney, while epx2b1 and epx2b2 were strongly expressed in the gills, and epx1 was not expressed in any of the tissues or organs analysed. In vitro stimulation of head kidney leucocytes with the parasite Philasterides dicentrarchi caused a decrease in mpx expression and an increase in epx2b1 expression over time. In turbot infected experimentally with P. dicentrarchi a significant increase in mpx expression in the head kidney was observed on day 7 postinfection, while the other genes were not regulated. However, mpx, epx2b1 and epx2b2 were downregulated in the gills of infected fish, and epx1 expression was not affected. These results suggest that the four genes responded differently to the same stimuli. Interestingly, BLAST analysis revealed that Epx1 and Mpx showed greater similarity to mammalian EPX than to MPO. Considering the phylogenetic and synteny data obtained, we concluded that the epx/mpx genes of Gnathostomes can be divided into three main clades: EPX1, which contains turbot epx1, EPX2, which contains turbot mpx (epx2a) and epx2b1 and epx2b2 genes, and a clade containing mammalian EPX and MPO (EPX/MPO). EPX/MPO and EPX2 clades share a common ancestor with the chondrichthyan elephant shark (Callorhinchus milii) and the coelacanth (Latimeria chalumnae) peroxidases. EPX2 was only found in fish and includes two sister groups. One of the groups includes turbot mpx and was only found in teleosts. Finally, the other group contains epx2b1 and epx2b2 genes, and epx2b1-2b2 loci share orthologous genes with other teleosts and also with holosteans, suggesting that these genes appeared earlier on than the mpx gene.gl
dc.description.peerreviewedSIgl
dc.description.sponsorshipThis study was financially supported by grant AGL2017-83577-R awarded by the Ministerio de Economía y Competitividad (Spain) and the European Regional Development Fund (ERDF, European Union), by grant ED431C2017/31 from the Xunta de Galicia (Spain) and by the PARAFISHCONTROL project, which received funding from the European Union's Horizon 2020 research and innovation programme under grant agreement no. 634429. FF-I was contracted by a grant from the Xunta de Galicia (Plan I2C)gl
dc.identifier.citationDev Comp Immunol. 2021 Jan 4;118:103993. doi: 10.1016/j.dci.2021.103993gl
dc.identifier.issn0145-305X
dc.identifier.issn10.1016/j.dci.2021.103993
dc.identifier.urihttp://hdl.handle.net/10347/24375
dc.language.isoenggl
dc.publisherElseviergl
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/H2020/634429
dc.relation.projectIDinfo:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/AGL2017-83577-R/ES/GENERACION DE VACUNAS RECOMBINANTES PARA LA INMUNOPROFILAXIS DE LA ESCUTICOCILIATOSIS DEL RODABALLO
dc.relation.publisherversionhttps://doi.org/10.1016/j.dci.2021.103993gl
dc.rights© 2021 Elsevier Ltd. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/gl
dc.rights.accessRightsopen accessgl
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectFishgl
dc.subjectTurbotgl
dc.subjectMyeloperoxidasegl
dc.subjectEosinophil peroxidasegl
dc.titleCharacterization of the turbot Scophthalmus maximus (L.) myeloperoxidase. An insight into the evolution of vertebrate peroxidasesgl
dc.typejournal articlegl
dc.type.hasVersionAMgl
dspace.entity.typePublication
relation.isAuthorOfPublication89a418f2-5b60-4a9f-bb1d-81ae1a20f438
relation.isAuthorOfPublication18414ba7-710a-4d0f-bf71-a494fc048c9b
relation.isAuthorOfPublication1405b8aa-a3ef-4048-938e-e53820a309b5
relation.isAuthorOfPublication.latestForDiscovery89a418f2-5b60-4a9f-bb1d-81ae1a20f438

Files

Original bundle

Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
Turbot myeloperoxidase.pdf
Size:
1.88 MB
Format:
Adobe Portable Document Format
Description: