Literature DB >> 8824188

Association of spindle assembly checkpoint component XMAD2 with unattached kinetochores.

R H Chen1, J C Waters, E D Salmon, A W Murray.   

Abstract

The spindle assembly checkpoint delays anaphase until all chromosomes are attached to a mitotic spindle. The mad (mitotic arrest-deficient) and bub (budding uninhibited by benzimidazole) mutants of budding yeast lack this checkpoint and fail to arrest the cell cycle when microtubules are depolymerized. A frog homolog of MAD2 (XMAD2) was isolated and found to play an essential role in the spindle assembly checkpoint in frog egg extracts. XMAD2 protein associated with unattached kinetochores in prometaphase and in nocodazole-treated cells and disappeared from kinetochores at metaphase in untreated cells, suggesting that XMAD2 plays a role in the activation of the checkpoint by unattached kinetochores. This study furthers understanding of the mechanism of cell cycle checkpoints in metazoa and provides a marker for studying the role of the spindle assembly checkpoint in the genetic instability of tumors.

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Year:  1996        PMID: 8824188     DOI: 10.1126/science.274.5285.242

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  186 in total

Review 1.  Control of mitotic transitions by the anaphase-promoting complex.

Authors:  G Fang; H Yu; M W Kirschner
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  1999-09-29       Impact factor: 6.237

2.  Proper metaphase spindle length is determined by centromere proteins Mis12 and Mis6 required for faithful chromosome segregation.

Authors:  G Goshima; S Saitoh; M Yanagida
Journal:  Genes Dev       Date:  1999-07-01       Impact factor: 11.361

3.  A MHC-encoded ubiquitin-like protein (FAT10) binds noncovalently to the spindle assembly checkpoint protein MAD2.

Authors:  Y C Liu; J Pan; C Zhang; W Fan; M Collinge; J R Bender; S M Weissman
Journal:  Proc Natl Acad Sci U S A       Date:  1999-04-13       Impact factor: 11.205

4.  Mad2 binding to Mad1 and Cdc20, rather than oligomerization, is required for the spindle checkpoint.

Authors:  L Sironi; M Melixetian; M Faretta; E Prosperini; K Helin; A Musacchio
Journal:  EMBO J       Date:  2001-11-15       Impact factor: 11.598

5.  Bub3 interaction with Mad2, Mad3 and Cdc20 is mediated by WD40 repeats and does not require intact kinetochores.

Authors:  R Fraschini; A Beretta; L Sironi; A Musacchio; G Lucchini; S Piatti
Journal:  EMBO J       Date:  2001-12-03       Impact factor: 11.598

6.  Microtubule-dependent changes in assembly of microtubule motor proteins and mitotic spindle checkpoint proteins at PtK1 kinetochores.

Authors:  D B Hoffman; C G Pearson; T J Yen; B J Howell; E D Salmon
Journal:  Mol Biol Cell       Date:  2001-07       Impact factor: 4.138

7.  CENP-H, a constitutive centromere component, is required for centromere targeting of CENP-C in vertebrate cells.

Authors:  T Fukagawa; Y Mikami; A Nishihashi; V Regnier; T Haraguchi; Y Hiraoka; N Sugata; K Todokoro; W Brown; T Ikemura
Journal:  EMBO J       Date:  2001-08-15       Impact factor: 11.598

8.  Creation and characterization of temperature-sensitive CENP-C mutants in vertebrate cells.

Authors:  T Fukagawa; V Regnier; T Ikemura
Journal:  Nucleic Acids Res       Date:  2001-09-15       Impact factor: 16.971

9.  CENP-E is essential for reliable bioriented spindle attachment, but chromosome alignment can be achieved via redundant mechanisms in mammalian cells.

Authors:  B F McEwen; G K Chan; B Zubrowski; M S Savoian; M T Sauer; T J Yen
Journal:  Mol Biol Cell       Date:  2001-09       Impact factor: 4.138

10.  Fission yeast ch-TOG/XMAP215 homologue Alp14 connects mitotic spindles with the kinetochore and is a component of the Mad2-dependent spindle checkpoint.

Authors:  M A Garcia; L Vardy; N Koonrugsa; T Toda
Journal:  EMBO J       Date:  2001-07-02       Impact factor: 11.598

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