Literature DB >> 15187257

A Xenopus cell-free system for analysis of the Chfr ubiquitin ligase involved in control of mitotic entry.

Dongmin Kang1, Jim Wong, Guowei Fang.   

Abstract

The checkpoint protein Chfr delays entry into mitosis in the presence of mitotic stress. We have analyzed the Chfr checkpoint pathway in the Xenopus cell-free system. We showed that Chfr is a ubiquitin ligase that targets polo-like kinase (Plk1) for degradation, leading to delayed activation of the Cdc25C phosphatase and prolonged inhibitory phosphorylation of Cdc2 at the G2/M transition. In this chapter, we will describe biochemical methods we developed to analyze the Chfr auto-ubiquitination activity and the ubiquitination of its substrate Plk1, as well as functional assays to investigate the Chfr pathway in Xenopus extracts.

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Year:  2004        PMID: 15187257     DOI: 10.1385/1-59259-788-2:229

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  3 in total

1.  The auto-ubiquitylation of E3 ubiquitin-protein ligase Chfr at G2 phase is required for accumulation of polo-like kinase 1 and mitotic entry in mammalian cells.

Authors:  Jo-Sun Kim; Yong-Yea Park; Sun-Yi Park; Hyeseon Cho; Dongmin Kang; Hyeseong Cho
Journal:  J Biol Chem       Date:  2011-07-15       Impact factor: 5.157

2.  Yeast Chfr homologs retard cell cycle at G1 and G2/M via Ubc4 and Ubc13/Mms2-dependent ubiquitination.

Authors:  Greta L Loring; Kathryn C Christensen; Scott A Gerber; Charles Brenner
Journal:  Cell Cycle       Date:  2007-10-02       Impact factor: 4.534

Review 3.  FHA-RING ubiquitin ligases in cell division cycle control.

Authors:  L Brooks; E G Heimsath; G L Loring; C Brenner
Journal:  Cell Mol Life Sci       Date:  2008-11       Impact factor: 9.261

  3 in total

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