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Conservation of the Nrf2-Mediated Gene Regulation of Proteasome Subunits and Glucose Metabolism in Zebrafish

The Keap1-Nrf2 system is an evolutionarily conserved defense mechanism against oxidative and xenobiotic stress. Besides the exogenous stress response, Nrf2 has been found to regulate numerous cellular functions, including protein turnover and glucose metabolism; however, the evolutionary origins of...

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Autores principales: Nguyen, Vu Thanh, Fuse, Yuji, Tamaoki, Junya, Akiyama, Shin-ichi, Muratani, Masafumi, Tamaru, Yutaka, Kobayashi, Makoto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5223048/
https://www.ncbi.nlm.nih.gov/pubmed/28116036
http://dx.doi.org/10.1155/2016/5720574
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author Nguyen, Vu Thanh
Fuse, Yuji
Tamaoki, Junya
Akiyama, Shin-ichi
Muratani, Masafumi
Tamaru, Yutaka
Kobayashi, Makoto
author_facet Nguyen, Vu Thanh
Fuse, Yuji
Tamaoki, Junya
Akiyama, Shin-ichi
Muratani, Masafumi
Tamaru, Yutaka
Kobayashi, Makoto
author_sort Nguyen, Vu Thanh
collection PubMed
description The Keap1-Nrf2 system is an evolutionarily conserved defense mechanism against oxidative and xenobiotic stress. Besides the exogenous stress response, Nrf2 has been found to regulate numerous cellular functions, including protein turnover and glucose metabolism; however, the evolutionary origins of these functions remain unknown. In the present study, we searched for novel target genes associated with the zebrafish Nrf2 to answer this question. A microarray analysis of zebrafish embryos that overexpressed Nrf2 revealed that 115 candidate genes were targets of Nrf2, including genes encoding proteasome subunits and enzymes involved in glucose metabolism. A real-time quantitative PCR suggested that the expression of 3 proteasome subunits (psma3, psma5, and psmb7) and 2 enzymes involved in glucose metabolism (pgd and fbp1a) were regulated by zebrafish Nrf2. We thus next examined the upregulation of these genes by an Nrf2 activator, diethyl maleate, using Nrf2 mutant zebrafish larvae. The results of real-time quantitative PCR and whole-mount in situ hybridization showed that all of these 5 genes were upregulated by diethyl maleate treatment in an Nrf2-dependent manner, especially in the liver. These findings implied that the Nrf2-mediated regulation of the proteasome subunits and glucose metabolism is evolutionarily conserved among vertebrates.
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spelling pubmed-52230482017-01-23 Conservation of the Nrf2-Mediated Gene Regulation of Proteasome Subunits and Glucose Metabolism in Zebrafish Nguyen, Vu Thanh Fuse, Yuji Tamaoki, Junya Akiyama, Shin-ichi Muratani, Masafumi Tamaru, Yutaka Kobayashi, Makoto Oxid Med Cell Longev Research Article The Keap1-Nrf2 system is an evolutionarily conserved defense mechanism against oxidative and xenobiotic stress. Besides the exogenous stress response, Nrf2 has been found to regulate numerous cellular functions, including protein turnover and glucose metabolism; however, the evolutionary origins of these functions remain unknown. In the present study, we searched for novel target genes associated with the zebrafish Nrf2 to answer this question. A microarray analysis of zebrafish embryos that overexpressed Nrf2 revealed that 115 candidate genes were targets of Nrf2, including genes encoding proteasome subunits and enzymes involved in glucose metabolism. A real-time quantitative PCR suggested that the expression of 3 proteasome subunits (psma3, psma5, and psmb7) and 2 enzymes involved in glucose metabolism (pgd and fbp1a) were regulated by zebrafish Nrf2. We thus next examined the upregulation of these genes by an Nrf2 activator, diethyl maleate, using Nrf2 mutant zebrafish larvae. The results of real-time quantitative PCR and whole-mount in situ hybridization showed that all of these 5 genes were upregulated by diethyl maleate treatment in an Nrf2-dependent manner, especially in the liver. These findings implied that the Nrf2-mediated regulation of the proteasome subunits and glucose metabolism is evolutionarily conserved among vertebrates. Hindawi Publishing Corporation 2016 2016-12-27 /pmc/articles/PMC5223048/ /pubmed/28116036 http://dx.doi.org/10.1155/2016/5720574 Text en
spellingShingle Research Article
Nguyen, Vu Thanh
Fuse, Yuji
Tamaoki, Junya
Akiyama, Shin-ichi
Muratani, Masafumi
Tamaru, Yutaka
Kobayashi, Makoto
Conservation of the Nrf2-Mediated Gene Regulation of Proteasome Subunits and Glucose Metabolism in Zebrafish
title Conservation of the Nrf2-Mediated Gene Regulation of Proteasome Subunits and Glucose Metabolism in Zebrafish
title_full Conservation of the Nrf2-Mediated Gene Regulation of Proteasome Subunits and Glucose Metabolism in Zebrafish
title_fullStr Conservation of the Nrf2-Mediated Gene Regulation of Proteasome Subunits and Glucose Metabolism in Zebrafish
title_full_unstemmed Conservation of the Nrf2-Mediated Gene Regulation of Proteasome Subunits and Glucose Metabolism in Zebrafish
title_short Conservation of the Nrf2-Mediated Gene Regulation of Proteasome Subunits and Glucose Metabolism in Zebrafish
title_sort conservation of the nrf2-mediated gene regulation of proteasome subunits and glucose metabolism in zebrafish
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5223048/
https://www.ncbi.nlm.nih.gov/pubmed/28116036
http://dx.doi.org/10.1155/2016/5720574
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