XPA deficiency affects the ubiquitin-proteasome system function
dc.contributor.author | Leal, Angélica Maria de Sousa | |
dc.contributor.author | Medeiros, Lázaro Batista de Azevedo | |
dc.contributor.author | Muñoz-Cadavid, Cesar Orlando | |
dc.contributor.author | Oliveira, Riva de Paula | |
dc.contributor.author | Timóteo, Ana Rafaela de Souza | |
dc.contributor.author | Oliveira, Ana Helena Sales de | |
dc.contributor.author | Faustino, André Luis Fonseca | |
dc.contributor.author | Silva, Vandeclécio Lira da | |
dc.contributor.author | Souza, Sandro José de | |
dc.contributor.author | Lajus, Tirzah Braz Petta | |
dc.contributor.author | Campos, Julliane Tamara Araújo de Melo | |
dc.contributor.author | Agnez-Lima, Lucymara Fassarella | |
dc.date.accessioned | 2020-07-23T17:36:23Z | |
dc.date.available | 2020-07-23T17:36:23Z | |
dc.date.issued | 2020-07 | |
dc.description.resumo | Xeroderma pigmentosum complementation group A (XPA), is defective in xeroderma pigmentosum patients, causing pre-disposition to skin cancer and neurological abnormalities, which is not well understood. Here, we analyzed the XPA-deficient cells transcriptional profile under oxidative stress. The imbalance in of ubiquitin-proteasome system (UPS) gene expression was observed in XPA-deficient cells and the involvement of nuclear factor erythroid 2-related factor-2 (NFE2L2) was indicated. Co-immunoprecipitation assays showed the interaction between XPA, apurinic-apyrimidinic endonuclease 1 (APE1) and NFE2L2 proteins. Decreased NFE2L2 protein expression and proteasome activity was also observed in XPA-deficient cells. The data suggest the involvement of the growth arrest and DNA-damage-inducible beta (GADD45β) in NFE2L2 functions. Similar results were obtained in xpa-1 (RNAi) Caenorhabditis elegans suggesting the conservation of XPA and NFE2L2 interactions. In conclusion, stress response activation occurs in XPA-deficient cells under oxidative stress; however, these cells fail to activate the UPS cytoprotective response, which may contribute to XPA patient’s phenotypes. | pt_BR |
dc.identifier.citation | LEAL, Angélica Maria de Sousa; MEDEIROS, Lázaro Batista de Azevedo; MUÑOZ-CADAVID, Cesar Orlando; OLIVEIRA, Riva de Paula; TIMÓTEO, Ana Rafaela de Souza; OLIVEIRA, Ana Helena Sales de; FAUSTINO, André Luis Fonseca; SILVA, Vandeclécio Lira da; SOUZA, Sandro José de; LAJUS, Tirzah Braz Petta. XPA deficiency affects the ubiquitin-proteasome system function. Dna Repair, [S.L.], v. 94, p. 102937, out. 2020. http://dx.doi.org/10.1016/j.dnarep.2020.102937. Disponível em: https://www.sciencedirect.com/science/article/abs/pii/S1568786420301865?via%3Dihub. Acesso em: 23 jul. 2020. | pt_BR |
dc.identifier.doi | 10.1016/j.dnarep.2020.102937 | |
dc.identifier.uri | https://repositorio.ufrn.br/jspui/handle/123456789/29716 | |
dc.language | en | pt_BR |
dc.publisher | Elsevier | pt_BR |
dc.rights | Attribution-NonCommercial-NoDerivs 3.0 Brazil | * |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/3.0/br/ | * |
dc.subject | Xeroderma pigmentosum | pt_BR |
dc.subject | Oxidative stress | pt_BR |
dc.subject | Xeroderma Pigmentosum Group A Protein | pt_BR |
dc.subject | Apurinic-apyrimidinic endonuclease 1 (APE1) | pt_BR |
dc.subject | NF-E2-Related Factor 2 | pt_BR |
dc.subject | Transcriptional regulation | pt_BR |
dc.subject | Proteolysis | pt_BR |
dc.subject | Proteostasis | pt_BR |
dc.subject | Proteasome | pt_BR |
dc.title | XPA deficiency affects the ubiquitin-proteasome system function | pt_BR |
dc.type | article | pt_BR |
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