Literature DB >> 11978736

A ubiquitin-proteasome system is responsible for the protection of yeast and human cells against methylmercury.

Gi-Wook Hwang1, Takemitsu Furuchi, Akira Naganuma.   

Abstract

The mechanism responsible for the toxic effects of methylmercury (MeHg), an important environmental pollutant, is poorly understood. We have identified a gene, CDC34, that confers resistance to MeHg in Saccharomyces cerevisiae by screening a yeast genomic DNA library. CDC34 encodes a ubiquitin-conjugating enzyme, Cdc34, which is involved in ubiquitin-dependent proteolysis. Overexpression of Cdc34 results in significant resistance to MeHg both in yeast and human cells, and it increases the cellular level of ubiquitinated proteins. The ubiquitin-conjugating activity of Cdc34 is essential for the Cdc34-mediated resistance to MeHg, and the protective effect of the overexpression of Cdc34 is depressed by inhibition of proteasome activity. Our results support the hypothesis that MeHg induces the cellular accumulation of a certain protein(s) that causes cell damage and that this protein(s) is degraded after its ubiquitination in proteasomes.

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Year:  2002        PMID: 11978736     DOI: 10.1096/fj.01-0899fje

Source DB:  PubMed          Journal:  FASEB J        ISSN: 0892-6638            Impact factor:   5.191


  9 in total

1.  Localizing organomercury uptake and accumulation in zebrafish larvae at the tissue and cellular level.

Authors:  Malgorzata Korbas; Scott R Blechinger; Patrick H Krone; Ingrid J Pickering; Graham N George
Journal:  Proc Natl Acad Sci U S A       Date:  2008-08-21       Impact factor: 11.205

2.  Methylmercury induced toxicogenomic response in C57 and SWV mouse embryos undergoing neural tube closure.

Authors:  Joshua F Robinson; William C Griffith; Xiaozhong Yu; Sungwoo Hong; Euvin Kim; Elaine M Faustman
Journal:  Reprod Toxicol       Date:  2010-05-20       Impact factor: 3.143

Review 3.  Neurotoxicity of organomercurial compounds.

Authors:  Coral Sanfeliu; Jordi Sebastià; Rosa Cristòfol; Eduard Rodríguez-Farré
Journal:  Neurotox Res       Date:  2003       Impact factor: 3.911

4.  Functions of yeast helicase Ssl2p that are essential for viability are also involved in protection from the toxicity of adriamycin.

Authors:  Takemitsu Furuchi; Tsutomu Takahashi; Shogo Tanaka; Katsushi Nitta; Akira Naganuma
Journal:  Nucleic Acids Res       Date:  2004-05-11       Impact factor: 16.971

5.  A system-based comparison of gene expression reveals alterations in oxidative stress, disruption of ubiquitin-proteasome system and altered cell cycle regulation after exposure to cadmium and methylmercury in mouse embryonic fibroblast.

Authors:  Xiaozhong Yu; Joshua F Robinson; Jaspreet S Sidhu; Sungwoo Hong; Elaine M Faustman
Journal:  Toxicol Sci       Date:  2010-01-08       Impact factor: 4.849

6.  Endoplasmic reticulum stress preconditioning attenuates methylmercury-induced cellular damage by inducing favorable stress responses.

Authors:  Fusako Usuki; Masatake Fujimura; Akio Yamashita
Journal:  Sci Rep       Date:  2013       Impact factor: 4.379

7.  Transport of pyruvate into mitochondria is involved in methylmercury toxicity.

Authors:  Jin-Yong Lee; Yosuke Ishida; Tsutomu Takahashi; Akira Naganuma; Gi-Wook Hwang
Journal:  Sci Rep       Date:  2016-02-22       Impact factor: 4.379

8.  The protein transportation pathway from Golgi to vacuoles via endosomes plays a role in enhancement of methylmercury toxicity.

Authors:  Gi-Wook Hwang; Yasutaka Murai; Tsutomu Takahashi; Akira Naganuma
Journal:  Sci Rep       Date:  2014-07-30       Impact factor: 4.379

Review 9.  Molecular Pathways Associated With Methylmercury-Induced Nrf2 Modulation.

Authors:  Takamitsu Unoki; Masahiro Akiyama; Yoshito Kumagai; Filipe Marques Gonçalves; Marcelo Farina; João Batista Teixeira da Rocha; Michael Aschner
Journal:  Front Genet       Date:  2018-09-12       Impact factor: 4.599

  9 in total

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