Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/96202
Title: Expression atlas of the Deubiquitinating enzymes in the adult mouse retina, their evolutionary diversification and phenotypic roles
Author: Esquerdo Barragán, Mariona
Grau Bové, Francesc Xavier
Garanto, Alejandro
Toulis, Vasileios
Garcia Monclús, Silvia
Millo, Erica
López-Iniesta, Mª José
Abad-Morales, Víctor
Ruiz Trillo, Iñaki
Marfany i Nadal, Gemma
Keywords: Ubiqüitina
Vertebrats
Retina
Fenotip
Ubiquitin
Vertebrates
Retina
Phenotype
Issue Date: 2-Mar-2016
Publisher: Public Library of Science (PLoS)
Abstract: Ubiquitination is a relevant cell regulatory mechanism to determine protein fate and function. Most data has focused on the role of ubiquitin as a tag molecule to target substrates to proteasome degradation, and on its impact in the control of cell cycle, protein homeostasis and cancer. Only recently, systematic assays have pointed to the relevance of the ubiquitin pathway in the development and differentiation of tissues and organs, and its implication in hereditary diseases. Moreover, although the activity and composition of ubiquitin ligases has been largely addressed, the role of the deubiquitinating enzymes (DUBs) in specific tissues, such as the retina, remains mainly unknown. In this work, we undertook a systematic analysis of the transcriptional levels of DUB genes in the adult mouse retina by RT-qPCR and analyzed the expression pattern by in situ hybridization and fluorescent immunohistochemistry, thus providing a unique spatial reference map of retinal DUB expression. We also performed a systematic phylogenetic analysis to understand the origin and the presence/absence of DUB genes in the genomes of diverse animal taxa that represent most of the known animal diversity. The expression landscape obtained supports the potential subfunctionalization of paralogs in those families that expanded in vertebrates. Overall, our results constitute a reference framework for further characterization of the DUB roles in the retina and suggest new candidates for inherited retinal disorders.
Note: Reproducció del document publicat a: http://dx.doi.org/10.1371/journal.pone.0150364
It is part of: PLoS One, 2016, vol. 11, num. 3, p. e0150364-e0150364
URI: http://hdl.handle.net/2445/96202
Related resource: http://dx.doi.org/10.1371/journal.pone.0150364
ISSN: 1932-6203
Appears in Collections:Articles publicats en revistes (Genètica, Microbiologia i Estadística)

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