| Literature DB >> 19656847 |
Stefano Cardinale1, Jan H Bergmann, David Kelly, Megumi Nakano, Manuel M Valdivia, Hiroshi Kimura, Hiroshi Masumoto, Vladimir Larionov, William C Earnshaw.
Abstract
We previously used a human artificial chromosome (HAC) with a synthetic kinetochore that could be targeted with chromatin modifiers fused to tetracycline repressor to show that targeting of the transcriptional repressor tTS within kinetochore chromatin disrupts kinetochore structure and function. Here we show that the transcriptional corepressor KAP1, a downstream effector of the tTS, can also inactivate the kinetochore. The disruption of kinetochore structure by KAP1 subdomains does not simply result from loss of centromeric CENP-A nucleosomes. Instead it reflects a hierarchical disruption of the outer kinetochore, with CENP-C levels falling before CENP-A levels and, in certain instances, CENP-H being lost more readily than CENP-C. These results suggest that this novel approach to kinetochore dissection may reveal new patterns of protein interactions within the kinetochore.Entities:
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Year: 2009 PMID: 19656847 PMCID: PMC2754933 DOI: 10.1091/mbc.e09-06-0489
Source DB: PubMed Journal: Mol Biol Cell ISSN: 1059-1524 Impact factor: 4.138