Cell cycle progression is driven by waves of cyclin expression coupled with regulated protein degradation. An essential step for initiating mitosis is the inactivation of proteolysis mediated by the anaphase-promoting complex/cyclosome (APC/C) bound to its regulator Cdh1p/Hct1p. Yeast APCCdh1 was proposed previously to be inactivated at Start by G1 cyclin/cyclin-dependent kinase (CDK). Here, we demonstrate that in a normal cell cycle APCCdh1 is inactivated in a graded manner and is not extinguished until S phase. Complete inactivation of APCCdh1 requires S phase cyclins. Further, persistent APCCdh1 activity throughout G1 helps to ensure the proper timing of Cdc20p expression. This suggests that S phase cyclins have an important role in allowing the accumulation of mitotic cyclins and further suggests a regulatory loop among S phase cyclins, APCCdh1, and APCCdc20.
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9 July 2001
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July 09 2001
Activity of the APCCdh1 form of the anaphase-promoting complex persists until S phase and prevents the premature expression of Cdc20p
James N. Huang,
James N. Huang
1Department of Pediatric Oncology, The Dana-Farber Cancer Institute
2Department of Pediatric Hematology, The Children's Hospital, Harvard Medical School, Boston, MA 02115
3Texas Children's Cancer Center, Department of Pediatrics, Baylor College of Medicine, Houston, TX 77030
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Iha Park,
Iha Park
1Department of Pediatric Oncology, The Dana-Farber Cancer Institute
2Department of Pediatric Hematology, The Children's Hospital, Harvard Medical School, Boston, MA 02115
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Eric Ellingson,
Eric Ellingson
1Department of Pediatric Oncology, The Dana-Farber Cancer Institute
2Department of Pediatric Hematology, The Children's Hospital, Harvard Medical School, Boston, MA 02115
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Laurie E. Littlepage,
Laurie E. Littlepage
1Department of Pediatric Oncology, The Dana-Farber Cancer Institute
2Department of Pediatric Hematology, The Children's Hospital, Harvard Medical School, Boston, MA 02115
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David Pellman
David Pellman
1Department of Pediatric Oncology, The Dana-Farber Cancer Institute
2Department of Pediatric Hematology, The Children's Hospital, Harvard Medical School, Boston, MA 02115
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James N. Huang
1Department of Pediatric Oncology, The Dana-Farber Cancer Institute
2Department of Pediatric Hematology, The Children's Hospital, Harvard Medical School, Boston, MA 02115
3Texas Children's Cancer Center, Department of Pediatrics, Baylor College of Medicine, Houston, TX 77030
Iha Park
1Department of Pediatric Oncology, The Dana-Farber Cancer Institute
2Department of Pediatric Hematology, The Children's Hospital, Harvard Medical School, Boston, MA 02115
Eric Ellingson
1Department of Pediatric Oncology, The Dana-Farber Cancer Institute
2Department of Pediatric Hematology, The Children's Hospital, Harvard Medical School, Boston, MA 02115
Laurie E. Littlepage
1Department of Pediatric Oncology, The Dana-Farber Cancer Institute
2Department of Pediatric Hematology, The Children's Hospital, Harvard Medical School, Boston, MA 02115
David Pellman
1Department of Pediatric Oncology, The Dana-Farber Cancer Institute
2Department of Pediatric Hematology, The Children's Hospital, Harvard Medical School, Boston, MA 02115
Address correspondence to David Pellman, Dana-Farber Cancer Institute/Harvard Medical School, Dept. of Pediatric Oncology, Rm. M612A, 44 Binney St., Boston, MA 02115. Tel.: (617) 632-4918. Fax: (617) 632-5757. E-mail: [email protected]
*
Abbreviations used in this paper: APC/C, anaphase-promoting complex/cyclosome; CDK, cyclin-dependent kinase; db, destruction box; GST, glutathione S-transferase; HA, hemagglutinin; YEP, yeast extract and peptone.
Received:
February 01 2001
Revision Received:
May 11 2001
Accepted:
May 25 2001
Online ISSN: 1540-8140
Print ISSN: 0021-9525
The Rockefeller University Press
2001
J Cell Biol (2001) 154 (1): 85–94.
Article history
Received:
February 01 2001
Revision Received:
May 11 2001
Accepted:
May 25 2001
Citation
James N. Huang, Iha Park, Eric Ellingson, Laurie E. Littlepage, David Pellman; Activity of the APCCdh1 form of the anaphase-promoting complex persists until S phase and prevents the premature expression of Cdc20p . J Cell Biol 9 July 2001; 154 (1): 85–94. doi: https://doi.org/10.1083/jcb.200102007
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