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dc.creatorKavouras M., Malandrakis E.E., Blom E., Tsilika K., Danis T., Panagiotaki P., Exadactylos A.en
dc.date.accessioned2023-01-31T08:34:26Z
dc.date.available2023-01-31T08:34:26Z
dc.date.issued2021
dc.identifier10.3390/ani11082273
dc.identifier.issn20762615
dc.identifier.urihttp://hdl.handle.net/11615/74699
dc.description.abstractIn farmed flatfish, such as common sole, color disturbances are common. Dyschromia is a general term that includes the color defects on the blind and ocular sides of the fish. The purpose was to examine the difference in gene expression between normal pigmented and juveniles who present ambicoloration. The analysis was carried out with next-generation sequencing techniques and de novo assembly of the transcriptome. Transcripts that showed significant differences (FDR < 0.05) in the expression between the two groups, were related to those of zebrafish (Danio rerio), functionally identified, and classified into categories of the gene ontology. The results revealed that ambicolorated juveniles exhibit a divergent function, mainly of the central nervous system at the synaptic level, as well as the ionic channels. The close association of chromophore cells with the growth of nerve cells and the nervous system was recorded. The pathway, glutamate binding–activation of AMPA and NMDA receptors–long-term stimulation of postsynaptic potential–LTP (long term potentiation)– plasticity of synapses, appears to be affected. In addition, the development of synapses also seems to be affected by the interaction of the LGI (leucine-rich glioma inactivated) protein family with the ADAM (a disintegrin and metalloprotease) ones. © 2021 by the authors. Licensee MDPI, Basel, Switzerland.en
dc.language.isoenen
dc.sourceAnimalsen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85111583619&doi=10.3390%2fani11082273&partnerID=40&md5=32e5b18f248f1eb8d3ac6f6f0c59ffae
dc.subjectMDPI AGen
dc.titleMalpigmentation of common sole (Solea solea) during metamorphosis is associated with differential synaptic-related gene expressionen
dc.typejournalArticleen


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