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Chromosoma. 2017 Aug;126(4):443-455. doi: 10.1007/s00412-016-0620-7. Epub 2016 Nov 17.

Structure of centromere chromatin: from nucleosome to chromosomal architecture.

Author information

1
Department of Molecular Biology, Sciences III, Institute of Genetics and Genomics of Geneva (iGE3), University of Geneva, Geneva, Switzerland. thomas.schalch@unige.ch.
2
Department of Molecular Biology, Sciences III, Institute of Genetics and Genomics of Geneva (iGE3), University of Geneva, Geneva, Switzerland. florian.steiner@unige.ch.

Abstract

The centromere is essential for the segregation of chromosomes, as it serves as attachment site for microtubules to mediate chromosome segregation during mitosis and meiosis. In most organisms, the centromere is restricted to one chromosomal region that appears as primary constriction on the condensed chromosome and is partitioned into two chromatin domains: The centromere core is characterized by the centromere-specific histone H3 variant CENP-A (also called cenH3) and is required for specifying the centromere and for building the kinetochore complex during mitosis. This core region is generally flanked by pericentric heterochromatin, characterized by nucleosomes containing H3 methylated on lysine 9 (H3K9me) that are bound by heterochromatin proteins. During mitosis, these two domains together form a three-dimensional structure that exposes CENP-A-containing chromatin to the surface for interaction with the kinetochore and microtubules. At the same time, this structure supports the tension generated during the segregation of sister chromatids to opposite poles. In this review, we discuss recent insight into the characteristics of the centromere, from the specialized chromatin structures at the centromere core and the pericentromere to the three-dimensional organization of these regions that make up the functional centromere.

KEYWORDS:

CENP-A; Centromere; Chromatin; Cohesin; Pericentromere

PMID:
27858158
PMCID:
PMC5509776
DOI:
10.1007/s00412-016-0620-7
[Indexed for MEDLINE]
Free PMC Article

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