The case for epigenetic effects on centromere identity and function

被引:387
作者
Karpen, GH
Allshire, RC
机构
[1] Salk Inst Biol Studies, Mol Biol & Virol Lab, La Jolla, CA 92037 USA
[2] Western Gen Hosp, MRC, Human Genet Unit, Chromosome Biol Sect, Edinburgh EH4 2XU, Midlothian, Scotland
关键词
D O I
10.1016/S0168-9525(97)01298-5
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The centromere is required to ensure the equal distribution of replicated chromosomes to daughter nuclei. Centromeres are frequently associated with heterochromatin, an enigmatic nuclear component that causes the epigenetic transcriptional repression of nearby marker genes (position-effect variegation of silencing). The process of chromosome segregation by movement along microtubules to spindle poles is highly conserved, yet the putative cis-acting centromeric DNA sequences bear little or no similarity across species. Recently, studies in several systems have revealed that the centromere itself might be epigenetically regulated and that the higher-order structure of the underlying heterochromatin contributes to centromere function and kinetochore assembly.
引用
收藏
页码:489 / 496
页数:8
相关论文
共 68 条