Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Comment
. 2007 Mar 12;176(6):735-6.
doi: 10.1083/jcb.200702020. Epub 2007 Mar 5.

Centromeric chromatin gets loaded

Affiliations
Comment

Centromeric chromatin gets loaded

Christopher W Carroll et al. J Cell Biol. .

Abstract

Centromeric nucleosomes contain a histone H3 variant called centromere protein A (CENP-A) that is required for kinetochore assembly and chromosome segregation. Two new studies, Jansen et al. (see p. 795 of this issue) and Maddox et al. (see p. 757 of this issue), address when CENP-A is deposited at centromeres during the cell division cycle and identify an evolutionally conserved protein required for CENP-A deposition. Together, these studies advance our understanding of centromeric chromatin assembly and provide a framework for investigating the molecular mechanisms that underlie the centromere-specific loading of CENP-A.

PubMed Disclaimer

Figures

Figure 1.
Figure 1.
A model for the centromere replication cycle for a single human chromosome. During DNA replication (1), CENP-A–containing nucleosomes (blue dots) are randomly distributed to each sister chromatid, resulting in a twofold reduction in the amount of CENP-A at each centromere. Upon exit from mitosis (2), a change in the state of KNL-2 or within the chromatin itself targets KNL-2 to the centromere, which, in turn, recruits newly synthesized CENP-A for deposition (3). After centromere replication, KNL-2 dissociates from centromeres (4). The mechanisms that control KNL-2 centromere binding and dissociation are unknown.

Comment on

References

    1. Carroll, C.W., and A.F. Straight. 2006. Centromere formation: from epigenetics to self-assembly. Trends Cell Biol. 16:70–78. - PubMed
    1. Cleveland, D.W., Y. Mao, and K.F. Sullivan. 2003. Centromeres and kinetochores: from epigenetics to mitotic checkpoint signaling. Cell. 112:407–421. - PubMed
    1. Fujita, Y., T. Hayashi, T. Kiyomitsu, Y. Toyoda, A. Kokubu, C. Obuse, and M. Yanagida. 2007. Priming of centromere for CENP-A recruitment by human hMis18alpha, hMis18beta, and M18BP1. Dev. Cell. 12:17–30. - PubMed
    1. Furuyama, T., Y. Dalal, and S. Henikoff. 2006. Chaperone-mediated assembly of centromeric chromatin in vitro. Proc. Natl. Acad. Sci. USA. 103:6172–6177. - PMC - PubMed
    1. Hayashi, T., Y. Fujita, O. Iwasaki, Y. Adachi, K. Takahashi, and M. Yanagida. 2004. Mis16 and Mis18 are required for CENP-A loading and histone deacetylation at centromeres. Cell. 118:715–729. - PubMed

MeSH terms