Positioning Heterochromatin at the Nuclear Periphery Suppresses Histone Turnover to Promote Epigenetic Inheritance

被引:85
作者
Holla, Sahana [1 ]
Dhakshnamoorthy, Jothy [1 ]
Folco, H. Diego [1 ]
Balachandran, Vanivilasini [1 ]
Xiao, Hua [1 ]
Sun, Ling-ling [1 ]
Wheeler, David [1 ]
Zofall, Martin [1 ]
Grewal, Shiv I. S. [1 ]
机构
[1] NCI, Lab Biochem & Mol Biol, NIH, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
MATING-TYPE REGION; FISSION YEAST; CHROMODOMAIN PROTEIN; MESSENGER-RNA; LYSINE-9; METHYLATION; NUCLEOSOME TURNOVER; PHASE-SEPARATION; HP1; PROTEINS; CELL FATE; CHROMATIN;
D O I
10.1016/j.cell.2019.12.004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In eukaryotes, heterochromatin is generally located at the nuclear periphery. This study investigates the biological significance of perinuclear positioning for heterochromatin maintenance and gene silencing. We identify the nuclear rim protein Amo1(NUPL2) as a factor required for the propagation of heterochromatin at endogenous and ectopic sites in the fission yeast genome. Amo1 associates with the Rix1(PELP1)-containing RNA processing complex RIXC and with the histone chaperone complex FACT. RIXC, which binds to heterochromatin protein Swi6(HP1) across silenced chromosomal domains and to surrounding boundary elements, connects heterochromatin with Amo1 at the nuclear periphery. In turn, the Amo1-enriched subdomain is critical for Swi6 association with FACT that precludes histone turnover to promote gene silencing and preserve epigenetic stability of heterochromatin. In addition to uncovering conserved factors required for perinuclear positioning of heterochromatin, these analyses elucidate a mechanism by which a peripheral subdomain enforces stable gene repression and maintains heterochromatin in a heritable manner.
引用
收藏
页码:150 / +
页数:30
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