NEDD8/Rub1 is a ubiquitin (Ub)-like molecule that covalently ligates to target proteins through an enzymatic cascade analogous to ubiquitylation. This modifier is known to target all cullin (Cul) family proteins. The latter are essential components of Skp1/Cul-1/F-box protein (SCF)–like Ub ligase complexes, which play critical roles in Ub-mediated proteolysis. To determine the role of the NEDD8 system in mammals, we generated mice deficient in Uba3 gene that encodes a catalytic subunit of NEDD8-activating enzyme. Uba3−/− mice died in utero at the periimplantation stage. Mutant embryos showed selective apoptosis of the inner cell mass but not of trophoblastic cells. However, the mutant trophoblastic cells could not enter the S phase of the endoreduplication cycle. This cell cycle arrest was accompanied with aberrant expression of cyclin E and p57Kip2. These results suggested that the NEDD8 system is essential for both mitotic and the endoreduplicative cell cycle progression. β-Catenin, a mediator of the Wnt/wingless signaling pathway, which degrades continuously in the cytoplasm through SCF Ub ligase, was also accumulated in the Uba3−/− cytoplasm and nucleus. Thus, the NEDD8 system is essential for the regulation of protein degradation pathways involved in cell cycle progression and morphogenesis, possibly through the function of the Cul family proteins.
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12 November 2001
Article|
November 05 2001
The NEDD8 system is essential for cell cycle progression and morphogenetic pathway in mice
Keisuke Tateishi,
Keisuke Tateishi
1Department of Molecular Oncology, Tokyo Metropolitan Institute of Medical Science, and CREST, Japan Science and Technology Corporation, Bunkyo-Ku, Tokyo 113-8613, Japan
2Department of Gastroenterology, Faculty of Medicine, University of Tokyo, Bunkyo-Ku, Tokyo 113-8655, Japan
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Masao Omata,
Masao Omata
2Department of Gastroenterology, Faculty of Medicine, University of Tokyo, Bunkyo-Ku, Tokyo 113-8655, Japan
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Keiji Tanaka,
Keiji Tanaka
1Department of Molecular Oncology, Tokyo Metropolitan Institute of Medical Science, and CREST, Japan Science and Technology Corporation, Bunkyo-Ku, Tokyo 113-8613, Japan
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Tomoki Chiba
Tomoki Chiba
1Department of Molecular Oncology, Tokyo Metropolitan Institute of Medical Science, and CREST, Japan Science and Technology Corporation, Bunkyo-Ku, Tokyo 113-8613, Japan
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Keisuke Tateishi
1Department of Molecular Oncology, Tokyo Metropolitan Institute of Medical Science, and CREST, Japan Science and Technology Corporation, Bunkyo-Ku, Tokyo 113-8613, Japan
2Department of Gastroenterology, Faculty of Medicine, University of Tokyo, Bunkyo-Ku, Tokyo 113-8655, Japan
Masao Omata
2Department of Gastroenterology, Faculty of Medicine, University of Tokyo, Bunkyo-Ku, Tokyo 113-8655, Japan
Keiji Tanaka
1Department of Molecular Oncology, Tokyo Metropolitan Institute of Medical Science, and CREST, Japan Science and Technology Corporation, Bunkyo-Ku, Tokyo 113-8613, Japan
Tomoki Chiba
1Department of Molecular Oncology, Tokyo Metropolitan Institute of Medical Science, and CREST, Japan Science and Technology Corporation, Bunkyo-Ku, Tokyo 113-8613, Japan
Address correspondence to Tomoki Chiba, Dept. of Molecular Oncology, Tokyo Metropolitan Institute of Medical Science, 3-18-22 Honkomagome, Bunkyo-Ku, Tokyo 113-8613, Japan. Tel. and fax: 81-3-3823-2237. E-mail: [email protected]
*
Abbreviations used in this paper: APC/C, anaphase-promoting complex/cyclosome; BAC, bacterial artificial chromosome; CDK, cyclin-dependent kinase; CKI, CDK inhibitor; Cul, cullin; E, embryonic day; ES, embryonic stem; H&E, hematoxylin and eosin; ICM, inner cell mass; PFA, paraformaldehyde; SCF, Skp1/Cul-1/F-box protein complex; TUNEL, TdT-mediated dUTP-biotin nick end labeling; Ub, ubiquitin; Wg, wingless; XP-E, xeroderma pigmentosa group E.
Received:
April 09 2001
Revision Received:
August 22 2001
Accepted:
October 02 2001
Online ISSN: 1540-8140
Print ISSN: 0021-9525
The Rockefeller University Press
2001
J Cell Biol (2001) 155 (4): 571–580.
Article history
Received:
April 09 2001
Revision Received:
August 22 2001
Accepted:
October 02 2001
Citation
Keisuke Tateishi, Masao Omata, Keiji Tanaka, Tomoki Chiba; The NEDD8 system is essential for cell cycle progression and morphogenetic pathway in mice . J Cell Biol 12 November 2001; 155 (4): 571–580. doi: https://doi.org/10.1083/jcb.200104035
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