Literature DB >> 10818100

Endoplasmic reticulum oxidoreductin 1-lbeta (ERO1-Lbeta), a human gene induced in the course of the unfolded protein response.

M Pagani1, M Fabbri, C Benedetti, A Fassio, S Pilati, N J Bulleid, A Cabibbo, R Sitia.   

Abstract

Oxidative conditions must be generated in the endoplasmic reticulum (ER) to allow disulfide bond formation in secretory proteins. A family of conserved genes, termed ERO for ER oxidoreductins, plays a key role in this process. We have previously described the human gene ERO1-L, which complements several phenotypic traits of the yeast thermo-sensitive mutant ero1-1 (Cabibbo, A., Pagani, M., Fabbri, M., Rocchi, M., Farmery, M. R., Bulleid, N. J., and Sitia, R. (2000) J. Biol. Chem. 275, 4827-4833). Here, we report the cloning and characterization of a novel human member of this family, ERO1-Lbeta. Immunofluorescence, endoglycosidase sensitivity, and in vitro translation/translocation assays reveal that the products of the ERO1-Lbeta gene are primarily localized in the ER of mammalian cells. The ability to allow growth at 37 degrees C and to alleviate the "unfolded protein response" when expressed in ero1-1 cells indicates that ERO1-Lbeta is involved also in generating oxidative conditions in the ER. ERO1-L and ERO1-Lbeta display different tissue distributions. Furthermore, only ERO1-Lbeta transcripts are induced in the course of the unfolded protein response. Our results suggest a complex regulation of ER redox homeostasis in mammalian cells.

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Year:  2000        PMID: 10818100     DOI: 10.1074/jbc.M003061200

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  98 in total

1.  Endoplasmic reticulum oxidase 1α is critical for collagen secretion from and membrane type 1-matrix metalloproteinase levels in hepatic stellate cells.

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Journal:  J Biol Chem       Date:  2017-08-03       Impact factor: 5.157

Review 2.  Redox-Mediated Regulatory Mechanisms of Endoplasmic Reticulum Homeostasis.

Authors:  Ryo Ushioda; Kazuhiro Nagata
Journal:  Cold Spring Harb Perspect Biol       Date:  2019-05-01       Impact factor: 10.005

3.  AtERO1 and AtERO2 Exhibit Differences in Catalyzing Oxidative Protein Folding in the Endoplasmic Reticulum.

Authors:  Fenggui Fan; Yini Zhang; Guozhong Huang; Qiao Zhang; Chih-Chen Wang; Lei Wang; Dongping Lu
Journal:  Plant Physiol       Date:  2019-05-28       Impact factor: 8.340

Review 4.  The endoplasmic reticulum and the unfolded protein response.

Authors:  Jyoti D Malhotra; Randal J Kaufman
Journal:  Semin Cell Dev Biol       Date:  2007-09-08       Impact factor: 7.727

Review 5.  The activities and function of molecular chaperones in the endoplasmic reticulum.

Authors:  Teresa M Buck; Christine M Wright; Jeffrey L Brodsky
Journal:  Semin Cell Dev Biol       Date:  2007-09-08       Impact factor: 7.727

Review 6.  Age-related cataracts: Role of unfolded protein response, Ca2+ mobilization, epigenetic DNA modifications, and loss of Nrf2/Keap1 dependent cytoprotection.

Authors:  Palsamy Periyasamy; Toshimichi Shinohara
Journal:  Prog Retin Eye Res       Date:  2017-08-31       Impact factor: 21.198

7.  Valproic acid suppresses Nrf2/Keap1 dependent antioxidant protection through induction of endoplasmic reticulum stress and Keap1 promoter DNA demethylation in human lens epithelial cells.

Authors:  Periyasamy Palsamy; Keshore R Bidasee; Toshimichi Shinohara
Journal:  Exp Eye Res       Date:  2014-02-10       Impact factor: 3.467

Review 8.  The oxidative protein folding machinery in plant cells.

Authors:  Isabel Aller; Andreas J Meyer
Journal:  Protoplasma       Date:  2012-10-23       Impact factor: 3.356

9.  Deregulation of pancreas-specific oxidoreductin ERO1β in the pathogenesis of diabetes mellitus.

Authors:  Motoharu Awazawa; Takashi Futami; Michinori Sakada; Kazuma Kaneko; Mitsuru Ohsugi; Keizo Nakaya; Ai Terai; Ryo Suzuki; Masato Koike; Yasuo Uchiyama; Takashi Kadowaki; Kohjiro Ueki
Journal:  Mol Cell Biol       Date:  2014-01-27       Impact factor: 4.272

Review 10.  Oxidative protein folding: from thiol-disulfide exchange reactions to the redox poise of the endoplasmic reticulum.

Authors:  Devin A Hudson; Shawn A Gannon; Colin Thorpe
Journal:  Free Radic Biol Med       Date:  2014-08-01       Impact factor: 7.376

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