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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
11
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pubmed:dateCreated |
1998-2-25
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pubmed:abstractText |
The trilaminar kinetochore directs the segregation of chromosomes in mitosis and meiosis. Despite its importance, the molecular architecture of this structure remains poorly understood [1]. The best known component of the kinetochore plates is CENP-C, a protein that is required for kinetochore assembly [2], but whose molecular role in kinetochore structure and function is unknown. Here we have raised for the first time monospecific antisera to CENP-A [3], a 17 kD centromere-specific histone variant that is 62% identical to the carboxy-terminal domain of histone H3 [4,5] and that resembles the yeast centromeric component CSE4 [6]. We have found by simultaneous immunofluorescence with centromere antigens of known ultrastructural location that CENP-A is concentrated in the region of the inner kinetochore plate at active centromeres. Because CENP-A was previously shown to co-purify with nucleosomes [7], our data suggest a specific nucleosomal substructure for the kinetochore. In human cells, these kinetochore-specific nucleosomes are enriched in alpha-satellite DNA [8]. However, the association of CENP-A with neocentromeres lacking detectable alpha-satellite DNA, and the lack of CENP-A association with alpha-satellite-rich inactive centromeres of dicentric chromosomes together suggest that CENP-A association with kinetochores is unlikely to be determined solely by DNA sequence recognition. We speculate that CENP-A binding could be a consequence of epigenetic tagging of mammalian centromeres.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Autoantibodies,
http://linkedlifedata.com/resource/pubmed/chemical/Autoantigens,
http://linkedlifedata.com/resource/pubmed/chemical/Chromosomal Proteins, Non-Histone,
http://linkedlifedata.com/resource/pubmed/chemical/Nucleosomes,
http://linkedlifedata.com/resource/pubmed/chemical/centromere protein A
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pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
0960-9822
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pubmed:author |
pubmed-author:BourassaSS,
pubmed-author:CookeC ACA,
pubmed-author:EarnshawW CWC,
pubmed-author:GimelliGG,
pubmed-author:PoirierG GGG,
pubmed-author:StettenGG,
pubmed-author:SullivanB ABA,
pubmed-author:SullivanK FKF,
pubmed-author:Tyler-SmithCC,
pubmed-author:VafaOO,
pubmed-author:WarburtonDD,
pubmed-author:WarburtonP EPE
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pubmed:issnType |
Print
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pubmed:day |
1
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pubmed:volume |
7
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
901-4
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:9382805-Amino Acid Sequence,
pubmed-meshheading:9382805-Autoantibodies,
pubmed-meshheading:9382805-Autoantigens,
pubmed-meshheading:9382805-Centromere,
pubmed-meshheading:9382805-Chromosomal Proteins, Non-Histone,
pubmed-meshheading:9382805-HeLa Cells,
pubmed-meshheading:9382805-Humans,
pubmed-meshheading:9382805-Kinetochores,
pubmed-meshheading:9382805-Molecular Sequence Data,
pubmed-meshheading:9382805-Nucleosomes
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pubmed:year |
1997
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pubmed:articleTitle |
Immunolocalization of CENP-A suggests a distinct nucleosome structure at the inner kinetochore plate of active centromeres.
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pubmed:affiliation |
Institute of Cell and Molecular Biology, University of Edinburgh, UK.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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