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Cold Spring Harbor Laboratory; 1999, Cold Spring Harbor Symposia on Quantitative Biology, 0(75), p. 403-418

DOI: 10.1101/sqb.2010.75.038

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Centromere Identity, Function, and Epigenetic Propagation Across Cell Divisions

Journal article published in 2010 by Ben E. Black, Lars E. T. Jansen, Daniel R. Foltz, Don W. Cleveland ORCID
This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

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Preprint: policy unknown
Question mark in circle
Postprint: policy unknown
Question mark in circle
Published version: policy unknown
Data provided by SHERPA/RoMEO

Abstract

The key to understanding centromere identity is likely to lie in the chromatin containing the histone H3 variant, CENP-A. CENP-A is the prime candidate to carry the epigenetic information that specifies the chromosomal location of the centromere in nearly all eukaryotic species, raising questions fundamental to understanding chromosome inheritance: How is the epigenetic centromere mark propagated? What physical properties of CENP-A-containing complexes are important for epigenetically marking centromeres? What are the molecules that recognize centromeric chromatin and serve as the foundation for the mitotic kinetochore? We discuss recent advances from our research groups that have yielded substantial insight into these questions and present our current understanding of the centromere. Future work promises an understanding of the molecular processes that confer fidelity to genome transmission at cell division.