Epigenomics of centromere assembly and function

被引:49
作者
Stimpson, Kaitlin M.
Sullivan, Beth A. [1 ]
机构
[1] Duke Univ, Duke Inst Genome Sci & Policy, Durham, NC 27708 USA
关键词
HUMAN ARTIFICIAL CHROMOSOME; ALPHA-SATELLITE DNA; CENP-A; DICENTRIC CHROMOSOME; ROBERTSONIAN TRANSLOCATIONS; SACCHAROMYCES-CEREVISIAE; MITOTIC RECOMBINATION; HISTONE MODIFICATIONS; INACTIVE CENTROMERE; HUMAN NEOCENTROMERE;
D O I
10.1016/j.ceb.2010.07.002
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The centromere is a complex chromosomal locus where the kinetochore is formed and microtubules attach during cell division. Centromere identity involves both genomic and sequence-independent (epigenetic) mechanisms. Current models for how centromeres are formed and, conversely, turned off have emerged from studies of unusual or engineered chromosomes, such as neocentromeres, artificial chromosomes, and dicentric chromosomes. Recent studies have highlighted the importance of unique chromatin marked by the histone H3 variant CENP-A, classical chromatin (heterochromatin and euchromatin), and transcription during centromere activation and inactivation. These advances have deepened our view of what defines a centromere and how it behaves in various genomic and chromatin contexts.
引用
收藏
页码:772 / 780
页数:9
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