Literature DB >> 9382804

Chromatin containing CENP-A and alpha-satellite DNA is a major component of the inner kinetochore plate.

O Vafa1, K F Sullivan.   

Abstract

The pathway of molecular interactions leading to kinetochore assembly on mammalian chromosomes is unknown. Kinetochores could be specified by structural features of centromeric satellite DNA [1-3] or by specific DNA sequences, analogous to budding yeast centromeres, interspersed in centromeric satellite DNA arrays [4,5]. Alternatively, kinetochores could be epigenetic structures that replicate without strict dependence on DNA sequence [6-8]. We purified kinetochore-associated chromatin from human chromosomes by immunoprecipitation of CENP-A, a centromere-specific histone H3 homologue located in the inner plate of the kinetochore [6,9,10]. Hybridization and DNA sequence analyses of cloned kinetochore DNA fragments revealed alpha-satellite as the predominant sequence associated with CENP-A. A major site of micrococcal nuclease digestion was identified by mapping the termini of alpha-satellite clones, suggesting that the inner kinetochore plate contains phased arrays of CENP-A-alpha-satellite nucleosomes. These experiments demonstrate for the first time that complex satellite DNA is a structural component of the kinetochore. Further, because complex satellite DNA is evolutionarily unconserved, these results suggest that molecular recognition events necessary for kinetochore formation take place at the level of DNA conformation or epigenetic mechanisms rather than DNA sequence per se.

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Year:  1997        PMID: 9382804     DOI: 10.1016/s0960-9822(06)00381-2

Source DB:  PubMed          Journal:  Curr Biol        ISSN: 0960-9822            Impact factor:   10.834


  77 in total

1.  Mapping of a human centromere onto the DNA by topoisomerase II cleavage.

Authors:  G Floridia; A Zatterale; O Zuffardi; C Tyler-Smith
Journal:  EMBO Rep       Date:  2000-12       Impact factor: 8.807

2.  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

3.  Neocentromeres and human artificial chromosomes: an unnatural act.

Authors:  H F Willard
Journal:  Proc Natl Acad Sci U S A       Date:  2001-05-08       Impact factor: 11.205

Review 4.  Chromatin proteins are determinants of centromere function.

Authors:  J A Sharp; P D Kaufman
Journal:  Curr Top Microbiol Immunol       Date:  2003       Impact factor: 4.291

Review 5.  RNA interference, transposons, and the centromere.

Authors:  R Kelly Dawe
Journal:  Plant Cell       Date:  2003-02       Impact factor: 11.277

6.  Sequence analysis of a functional Drosophila centromere.

Authors:  Xiaoping Sun; Hiep D Le; Janice M Wahlstrom; Gary H Karpen
Journal:  Genome Res       Date:  2003-02       Impact factor: 9.043

7.  Functional rice centromeres are marked by a satellite repeat and a centromere-specific retrotransposon.

Authors:  Zhukuan Cheng; Fenggao Dong; Tim Langdon; Shu Ouyang; C Robin Buell; Minghong Gu; Frederick R Blattner; Jiming Jiang
Journal:  Plant Cell       Date:  2002-08       Impact factor: 11.277

8.  Localisation of centromeric proteins to a fraction of mouse minor satellite DNA on a mini-chromosome in human, mouse and chicken cells.

Authors:  Kang Zeng; Jose I de las Heras; Andrew Ross; Jian Yang; Howard Cooke; Ming Hong Shen
Journal:  Chromosoma       Date:  2004-07-28       Impact factor: 4.316

Review 9.  Establishment of the vertebrate kinetochores.

Authors:  Tetsuya Hori; Tatsuo Fukagawa
Journal:  Chromosome Res       Date:  2012-07       Impact factor: 5.239

Review 10.  Understanding eukaryotic chromosome segregation from a comparative biology perspective.

Authors:  Snezhana Oliferenko
Journal:  J Cell Sci       Date:  2018-07-20       Impact factor: 5.285

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