p53 is a transcription factor that induces growth arrest or apoptosis in response to cellular stress. To identify new p53-inducible proapoptotic genes, we compared, by differential display, the expression of genes in spleen or thymus of normal and p53 nullizygote mice after γ-irradiation of whole animals. We report the identification and characterization of human and mouse Scotin homologues, a novel gene directly transactivated by p53. The Scotin protein is localized to the ER and the nuclear membrane. Scotin can induce apoptosis in a caspase-dependent manner. Inhibition of endogenous Scotin expression increases resistance to p53-dependent apoptosis induced by DNA damage, suggesting that Scotin plays a role in p53-dependent apoptosis. The discovery of Scotin brings to light a role of the ER in p53-dependent apoptosis.
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22 July 2002
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July 22 2002
Scotin, a novel p53-inducible proapoptotic protein located in the ER and the nuclear membrane
J.-C. Bourdon,
J.-C. Bourdon
Department of Surgery and Molecular Oncology, Ninewells Hospital and Medical School, Cancer Research Campaign (CRC) Cell Transformation Research Group, University of Dundee, Dundee DD1 9SY, UK
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J. Renzing,
J. Renzing
Department of Surgery and Molecular Oncology, Ninewells Hospital and Medical School, Cancer Research Campaign (CRC) Cell Transformation Research Group, University of Dundee, Dundee DD1 9SY, UK
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P.L. Robertson,
P.L. Robertson
Department of Surgery and Molecular Oncology, Ninewells Hospital and Medical School, Cancer Research Campaign (CRC) Cell Transformation Research Group, University of Dundee, Dundee DD1 9SY, UK
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K.N. Fernandes,
K.N. Fernandes
Department of Surgery and Molecular Oncology, Ninewells Hospital and Medical School, Cancer Research Campaign (CRC) Cell Transformation Research Group, University of Dundee, Dundee DD1 9SY, UK
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D.P. Lane
D.P. Lane
Department of Surgery and Molecular Oncology, Ninewells Hospital and Medical School, Cancer Research Campaign (CRC) Cell Transformation Research Group, University of Dundee, Dundee DD1 9SY, UK
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J.-C. Bourdon
Department of Surgery and Molecular Oncology, Ninewells Hospital and Medical School, Cancer Research Campaign (CRC) Cell Transformation Research Group, University of Dundee, Dundee DD1 9SY, UK
J. Renzing
Department of Surgery and Molecular Oncology, Ninewells Hospital and Medical School, Cancer Research Campaign (CRC) Cell Transformation Research Group, University of Dundee, Dundee DD1 9SY, UK
P.L. Robertson
Department of Surgery and Molecular Oncology, Ninewells Hospital and Medical School, Cancer Research Campaign (CRC) Cell Transformation Research Group, University of Dundee, Dundee DD1 9SY, UK
K.N. Fernandes
Department of Surgery and Molecular Oncology, Ninewells Hospital and Medical School, Cancer Research Campaign (CRC) Cell Transformation Research Group, University of Dundee, Dundee DD1 9SY, UK
D.P. Lane
Department of Surgery and Molecular Oncology, Ninewells Hospital and Medical School, Cancer Research Campaign (CRC) Cell Transformation Research Group, University of Dundee, Dundee DD1 9SY, UK
Address correspondence to D.P. Lane, Dept. of Surgery and Molecular Oncology, Ninewells Hospital and Medical School, CRC Cell Transformation Research Group, University of Dundee, Dundee DD1 9SY, UK. Tel.: 44-1382-496362. Fax: 44-1382-496363. E-mail: [email protected]
J. Renzig's present address is Roche Diagnosis GmbH, Nonnenwald 2, 82372 Penzberg, Germany.
*
Abbreviations used in this paper: Ad, adenovirus; AS, antisense; EMSA, electrophoretic mobility shift assay; MEF, mouse embryonic fibroblast; p53−/−, p53 nullizygote; p53+/+, p53 homozygote; RACE, rapid amplification of cDNA ends; UTR, untranslated region; wt, wild-type.
Received:
March 01 2002
Revision Received:
May 31 2002
Accepted:
May 31 2002
Online ISSN: 1540-8140
Print ISSN: 0021-9525
The Rockefeller University Press
2002
J Cell Biol (2002) 158 (2): 235–246.
Article history
Received:
March 01 2002
Revision Received:
May 31 2002
Accepted:
May 31 2002
Citation
J.-C. Bourdon, J. Renzing, P.L. Robertson, K.N. Fernandes, D.P. Lane; Scotin, a novel p53-inducible proapoptotic protein located in the ER and the nuclear membrane . J Cell Biol 22 July 2002; 158 (2): 235–246. doi: https://doi.org/10.1083/jcb.200203006
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