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Emi1 is required for cytostatic factor arrest in vertebrate eggs

Vertebrate eggs are arrested at metaphase of meiosis II with stable cyclin B and high cyclin B/Cdc2 kinase activity. The ability of the anaphase-promoting complex/cyclosome (APC), an E3 ubiquitin ligase, to trigger cyclin B destruction and metaphase exit is blocked in eggs by the activity of cytosta...

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Published in:Nature (London) 2002-04, Vol.416 (6883), p.850-854
Main Authors: Jackson, Peter K, Reimann, Julie D. R
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description Vertebrate eggs are arrested at metaphase of meiosis II with stable cyclin B and high cyclin B/Cdc2 kinase activity. The ability of the anaphase-promoting complex/cyclosome (APC), an E3 ubiquitin ligase, to trigger cyclin B destruction and metaphase exit is blocked in eggs by the activity of cytostatic factor (CSF) (reviewed in ref. 1). CSF was defined as an activity in mature oocytes that caused mitotic arrest when injected into dividing embryos. Fertilization causes a transient increase in cytoplasmic calcium concentration leading to CSF inactivation, APC activation, cyclin B destruction and mitotic exit. The APC activator Cdc20 is required for APC activation after fertilization. We show here that the APCcdc20 inhibitor Emi1 (ref. 6) is necessary and sufficient to inhibit the APC and to prevent mitotic exit in CSF-arrested eggs. CSF extracts immunodepleted of Emi1 degrade cyclin B, and exit from mitosis prematurely in the absence of calcium. Addition of Emi1 to these Emi1-depleted extracts blocks premature inactivation of the CSF-arrested state. Emi1 is required to arrest unfertilized eggs at metaphase of meiosis II and seems to be the long-sought mediator of CSF activity.
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R</creator><creatorcontrib>Jackson, Peter K ; Reimann, Julie D. R</creatorcontrib><description>Vertebrate eggs are arrested at metaphase of meiosis II with stable cyclin B and high cyclin B/Cdc2 kinase activity. The ability of the anaphase-promoting complex/cyclosome (APC), an E3 ubiquitin ligase, to trigger cyclin B destruction and metaphase exit is blocked in eggs by the activity of cytostatic factor (CSF) (reviewed in ref. 1). CSF was defined as an activity in mature oocytes that caused mitotic arrest when injected into dividing embryos. Fertilization causes a transient increase in cytoplasmic calcium concentration leading to CSF inactivation, APC activation, cyclin B destruction and mitotic exit. The APC activator Cdc20 is required for APC activation after fertilization. We show here that the APCcdc20 inhibitor Emi1 (ref. 6) is necessary and sufficient to inhibit the APC and to prevent mitotic exit in CSF-arrested eggs. CSF extracts immunodepleted of Emi1 degrade cyclin B, and exit from mitosis prematurely in the absence of calcium. Addition of Emi1 to these Emi1-depleted extracts blocks premature inactivation of the CSF-arrested state. 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Psychology ; Inactivation ; Meiosis - drug effects ; Mitogen-Activated Protein Kinases - metabolism ; Models, Biological ; Oocytes - cytology ; Oocytes - drug effects ; Oocytes - metabolism ; Precipitin Tests ; Proteins ; Proto-Oncogene Proteins c-mos - genetics ; Proto-Oncogene Proteins c-mos - metabolism ; Rats ; Saccharomyces cerevisiae Proteins ; Signal Transduction ; Vertebrates ; Xenopus laevis - metabolism ; Xenopus Proteins</subject><ispartof>Nature (London), 2002-04, Vol.416 (6883), p.850-854</ispartof><rights>2002 INIST-CNRS</rights><rights>COPYRIGHT 2002 Nature Publishing Group</rights><rights>Copyright Macmillan Journals Ltd. 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Fertilization causes a transient increase in cytoplasmic calcium concentration leading to CSF inactivation, APC activation, cyclin B destruction and mitotic exit. The APC activator Cdc20 is required for APC activation after fertilization. We show here that the APCcdc20 inhibitor Emi1 (ref. 6) is necessary and sufficient to inhibit the APC and to prevent mitotic exit in CSF-arrested eggs. CSF extracts immunodepleted of Emi1 degrade cyclin B, and exit from mitosis prematurely in the absence of calcium. Addition of Emi1 to these Emi1-depleted extracts blocks premature inactivation of the CSF-arrested state. Emi1 is required to arrest unfertilized eggs at metaphase of meiosis II and seems to be the long-sought mediator of CSF activity.</abstract><cop>London</cop><pub>Nature Publishing</pub><pmid>11976684</pmid><doi>10.1038/416850a</doi><tpages>5</tpages></addata></record>
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subjects anaphase-promoting complex
Animals
APC protein
Biological and medical sciences
Calcium
Calcium - metabolism
Calcium - pharmacology
Cdc20 protein
Cdc20 Proteins
Cell Cycle - drug effects
Cell Cycle Proteins - antagonists & inhibitors
Cell Cycle Proteins - genetics
Cell Cycle Proteins - metabolism
Cell Extracts
Cyclin B - metabolism
cytostatic factor
Early stages. Segmentation. Gastrulation. Neurulation
Eggs
Embryology: invertebrates and vertebrates. Teratology
Embryos
Emi1 gene
Fundamental and applied biological sciences. Psychology
Inactivation
Meiosis - drug effects
Mitogen-Activated Protein Kinases - metabolism
Models, Biological
Oocytes - cytology
Oocytes - drug effects
Oocytes - metabolism
Precipitin Tests
Proteins
Proto-Oncogene Proteins c-mos - genetics
Proto-Oncogene Proteins c-mos - metabolism
Rats
Saccharomyces cerevisiae Proteins
Signal Transduction
Vertebrates
Xenopus laevis - metabolism
Xenopus Proteins
title Emi1 is required for cytostatic factor arrest in vertebrate eggs
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