Calcium triggers exit from meiosis II by targeting the APC/C inhibitor XErp1 for degradation (original) (raw)
References
Tunquist, B. J. & Maller, J. L. Under arrest: cytostatic factor (CSF)-mediated metaphase arrest in vertebrate eggs. Genes Dev.17, 683–710 (2003) ArticleCAS Google Scholar
Masui, Y. & Markert, C. L. Cytoplasmic control of nuclear behaviour during meiotic maturation of frog oocytes. J. Exp. Zool.177, 129–145 (1971) ArticleCAS Google Scholar
King, R. W. et al. A 20S complex containing CDC27 and CDC15 catalyzes the mitosis-specific conjugation of ubiquitin to cyclin B. Cell81, 279–288 (1995) ArticleCAS Google Scholar
Sudakin, V. et al. The cyclosome, a large complex containing cyclin-selective ubiquitin ligase activity, targets cyclins for destruction at the end of mitosis. Mol. Biol. Cell6, 185–197 (1995) ArticleCAS Google Scholar
Salah, S. M. & Nasmyth, K. Destruction of the securin Pds1p occurs at the onset of anaphase during both meiotic divisions in yeast. Chromosoma109, 27–34 (2000) ArticleCAS Google Scholar
Busa, W. B. & Nuccitelli, R. An elevated free cytosolic Ca2+ wave follows fertilization in eggs of the frog, Xenopus laevis. J. Cell Biol.100, 1325–1329 (1985) ArticleCAS Google Scholar
Lorca, T. et al. Degradation of the proto-oncogene product p39mos is not necessary for cyclin proteolysis and exit from meiotic metaphase: requirement for a Ca(2 + )-calmodulin dependent event. EMBO J.10, 2087–2093 (1991) ArticleCAS Google Scholar
Lorca, T. et al. Calmodulin-dependent protein kinase II mediates inactivation of MPF and CSF upon fertilization of Xenopus eggs. Nature366, 270–273 (1993) ArticleADSCAS Google Scholar
Schmidt, A. et al. Xenopus polo-like kinase Plx1 regulates XErp1, a novel inhibitor of APC/C activity. Genes Dev.19, 502–513 (2005) ArticleCAS Google Scholar
Fuchs, S. Y., Spiegelman, V. S. & Kumar, K. G. The many faces of beta-TrCP E3 ubiquitin ligases: reflections in the magic mirror of cancer. Oncogene23, 2028–2036 (2004) ArticleCAS Google Scholar
Descombes, P. & Nigg, E. A. The polo-like kinase Plx1 is required for M phase exit and destruction of mitotic regulators in Xenopus egg extracts. EMBO J.17, 1328–1335 (1998) ArticleCAS Google Scholar
Elia, A. E., Cantley, L. C. & Yaffe, M. B. Proteomic screen finds pSer/pThr-binding domain localizing Plk1 to mitotic substrates. Science299, 1228–1231 (2003) ArticleADSCAS Google Scholar
Elia, A. E. et al. The molecular basis for phosphodependent substrate targeting and regulation of Plks by the Polo-box domain. Cell115, 83–95 (2003) ArticleCAS Google Scholar
Holloway, S. L., Glotzer, M., King, R. W. & Murray, A. W. Anaphase is initiated by proteolysis rather than by the inactivation of maturation-promoting factor. Cell73, 13393–13402 (1993) Article Google Scholar
Stemmann, O., Zou, H., Gerber, S. A., Gygi, S. P. & Kirschner, M. W. Dual inhibition of sister chromatid separation at metaphase. Cell107, 715–726 (2001) ArticleCAS Google Scholar
Colbran, R. J., Fong, Y. L., Schworer, C. M. & Soderling, T. R. Regulatory interactions of the calmodulin-binding, inhibitory, and autophosphorylation domains of Ca2+/calmodulin-dependent protein kinase II. J. Biol. Chem.263, 18145–18151 (1988) CASPubMed Google Scholar
Zachariae, W. Emi1 and Erp1: who can stop these eggs? Dev. Cell8, 301–303 (2005) ArticleCAS Google Scholar
Ohsumi, K., Koyanagi, A., Yamamoto, T. M., Gotoh, T. & Kishimoto, T. Emi1-mediated M-phase arrest in Xenopus eggs is distinct from cytostatic factor arrest. Proc. Natl Acad. Sci. USA101, 12531–12536 (2004) ArticleADSCAS Google Scholar
Tung, J. J. et al. A role for the anaphase-promoting complex inhibitor Emi2/XErp1, a homolog of early mitotic inhibitor 1, in cytostatic factor arrest of Xenopus eggs. Proc. Natl Acad. Sci. USA102, 4318–4323 (2005) ArticleADSCAS Google Scholar
Desai, A., Murray, A., Mitchison, T. J. & Walczak, C. E. The use of Xenopus egg extracts to study mitotic spindle assembly and function in vitro. Methods Cell Biol.61, 385–412 (1999) ArticleCAS Google Scholar
Funabiki, H. & Murray, A. W. The Xenopus chromokinesin Xkid is essential for metaphase chromosome alignment and must be degraded to allow anaphase chromosome movement. Cell102, 411–424 (2000) ArticleCAS Google Scholar