Centromeric Heterochromatin: The Primordial Segregation Machine

被引:56
作者
Bloom, Kerry S. [1 ]
机构
[1] Univ N Carolina, Dept Biol, Chapel Hill, NC 27599 USA
来源
ANNUAL REVIEW OF GENETICS, VOL 48 | 2014年 / 48卷
关键词
centromere; heterochromatin; chromosome segregation; DNA mechanics; molecular springs; SISTER-CHROMATID COHESION; PRESSURE-INDUCED DEPOLYMERIZATION; SPINDLE-ASSEMBLY CHECKPOINT; BUDDING YEAST CHROMOSOMES; 2 MICRON PLASMID; SACCHAROMYCES-CEREVISIAE; FISSION-YEAST; CENP-A; MOLECULAR ARCHITECTURE; PERICENTRIC CHROMATIN;
D O I
10.1146/annurev-genet-120213-092033
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Centromeres are specialized domains of heterochromatin that provide the foundation for the kinetochore. Centromeric heterochromatin is characterized by specific histone modifications, a centromere-specific histone H3 variant (CENP-A), and the enrichment of cohesin, condensin, and topoisomerase II. Centromere DNA varies orders of magnitude in size from 125 bp (budding yeast) to several megabases (human). In metaphase, sister kinetochores on the surface of replicated chromosomes face away from each other, where they establish microtubule attachment and bi-orientation. Despite the disparity in centromere size, the distance between separated sister kinetochores is remarkably conserved (approximately 1 mu m) throughout phylogeny. The centromere functions as a molecular spring that resists microtubule-based extensional forces in mitosis. This review explores the physical properties of DNA in order to understand how the molecular spring is built and how it contributes to the fidelity of chromosome segregation.
引用
收藏
页码:457 / 484
页数:28
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