Literature DB >> 7690762

Differential expression of a phosphoepitope at the kinetochores of moving chromosomes.

G J Gorbsky1, W A Ricketts.   

Abstract

A phosphorylated epitope is differentially expressed at the kinetochores of chromosomes in mitotic cells and may be involved in regulating chromosome movement and cell cycle progression. During prophase and early prometaphase, the phosphoepitope is expressed equally among all the kinetochores. In mid-prometaphase, some chromosomes show strong labeling on both kinetochores; others exhibit weak or no labeling; while in other chromosomes, one kinetochore is intensely labeled while its sister kinetochore is unlabeled. Chromosomes moving toward the metaphase plate express the phosphoepitope strongly on the leading kinetochore but weakly on the trailing kinetochore. This is the first demonstration of a biochemical difference between the two kinetochores of a single chromosome. During metaphase and anaphase, the kinetochores are unlabeled. At metaphase, a single misaligned chromosome can inhibit further progression into anaphase. Misaligned chromosomes express the phosphoepitope strongly on both kinetochores, even when all the other chromosomes of a cell are assembled at the metaphase plate and lack expression. This phosphoepitope may be involved in regulating chromosome movement to the metaphase plate during prometaphase and may be part of a cell cycle checkpoint by which the onset of anaphase is inhibited until complete metaphase alignment is achieved.

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Year:  1993        PMID: 7690762      PMCID: PMC2119849          DOI: 10.1083/jcb.122.6.1311

Source DB:  PubMed          Journal:  J Cell Biol        ISSN: 0021-9525            Impact factor:   10.539


  52 in total

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Journal:  Nature       Date:  1990-05-17       Impact factor: 49.962

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Journal:  Nature       Date:  1990-05-17       Impact factor: 49.962

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Journal:  J Cell Biol       Date:  1992-03       Impact factor: 10.539

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  76 in total

1.  The consequences of a non-uniform tension across kinetochores: lessons from segregation of chromosomes in the permanent translocation heterozygote Oenothera.

Authors:  Z Hejnowicz; L J Feldman
Journal:  Chromosome Res       Date:  2000       Impact factor: 5.239

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Authors:  Susan L Kline-Smith; Alexey Khodjakov; Polla Hergert; Claire E Walczak
Journal:  Mol Biol Cell       Date:  2003-12-29       Impact factor: 4.138

Review 5.  Chromosomal passengers: the four-dimensional regulation of mitotic events.

Authors:  Paola Vagnarelli; William C Earnshaw
Journal:  Chromosoma       Date:  2004-09-04       Impact factor: 4.316

Review 6.  Monitoring the fidelity of mitotic chromosome segregation by the spindle assembly checkpoint.

Authors:  P Silva; J Barbosa; A V Nascimento; J Faria; R Reis; H Bousbaa
Journal:  Cell Prolif       Date:  2011-10       Impact factor: 6.831

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Journal:  Proc Natl Acad Sci U S A       Date:  1997-08-19       Impact factor: 11.205

8.  Kinetochore rearrangement in meiosis II requires attachment to the spindle.

Authors:  Leocadia V Paliulis; R Bruce Nicklas
Journal:  Chromosoma       Date:  2005-02-12       Impact factor: 4.316

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Authors:  John R Daum; Gary J Gorbsky
Journal:  Methods       Date:  2006-01       Impact factor: 3.608

10.  Cellular expression of human centromere protein C demonstrates a cyclic behavior with highest abundance in the G1 phase.

Authors:  M Knehr; M Poppe; D Schroeter; W Eickelbaum; E M Finze; U L Kiesewetter; M Enulescu; M Arand; N Paweletz
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