The quantitative architecture of centromeric chromatin

Dani L. Bodor(Instituto Gulbenkian de Ciência), João F. Mata(Instituto Gulbenkian de Ciência), Mikhail Sergeev(Brigham and Women's Hospital), Ana F. David(Instituto Gulbenkian de Ciência), Kevan J. Salimian(University of Pennsylvania), Tanya Panchenko(University of Pennsylvania), Don W. Cleveland(University of California San Diego), Ben E. Black(University of Pennsylvania), Jagesh V. Shah(Brigham and Women's Hospital), Lars E.T. Jansen(Instituto Gulbenkian de Ciência)
eLife
July 15, 2014
Cited by 239Open Access
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Abstract

The centromere, responsible for chromosome segregation during mitosis, is epigenetically defined by CENP-A containing chromatin. The amount of centromeric CENP-A has direct implications for both the architecture and epigenetic inheritance of centromeres. Using complementary strategies, we determined that typical human centromeres contain ∼400 molecules of CENP-A, which is controlled by a mass-action mechanism. This number, despite representing only ∼4% of all centromeric nucleosomes, forms a ∼50-fold enrichment to the overall genome. In addition, although pre-assembled CENP-A is randomly segregated during cell division, this amount of CENP-A is sufficient to prevent stochastic loss of centromere function and identity. Finally, we produced a statistical map of CENP-A occupancy at a human neocentromere and identified nucleosome positions that feature CENP-A in a majority of cells. In summary, we present a quantitative view of the centromere that provides a mechanistic framework for both robust epigenetic inheritance of centromeres and the paucity of neocentromere formation.DOI: http://dx.doi.org/10.7554/eLife.02137.001.


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