Spatial segregation of heterochromatin: Uncovering functionality in a multicellular organism

被引:16
作者
Cabianca, Daphne S. [1 ]
Gasser, Susan M. [1 ,2 ]
机构
[1] Friedrich Miescher Inst Biomed Res, Maulbeerstr 66, CH-4048 Basel, Switzerland
[2] Univ Basel, Fac Nat Sci, Basel, Switzerland
基金
瑞士国家科学基金会;
关键词
C; elegans; CEC-4; cell fate; H3K9; methylation; Heterochromatin; nuclear periphery; NUCLEAR LAMINA INTERACTIONS; CELL FATE; STEM-CELLS; CHROMATIN; ENVELOPE; COMPARTMENTALIZATION; DIFFERENTIATION; PROTEINS; REORGANIZATION; CHROMOSOMES;
D O I
10.1080/19491034.2016.1187354
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Multiple layers of regulation are required to ensure appropriate patterns of gene expression for accurate cell differentiation. Interphase chromatin is non-randomly distributed within the nucleus, with highly compacted, transcriptionally silent heterochromatin enriched at the nuclear and nucleolar periphery. Whether this spatial organization serves a function in organismal physiology, rather than simply being a byproduct of chromatin metabolism, is a fundamental question. Recent work performed in C. elegans embryos characterized the molecular mechanisms that drive the perinuclear anchoring of heterochromatin. Moreover, for the first time it was shown that heterochromatin sequestration helps to restrict cell differentiation programs, while sustaining commitment to a specified fate. Here, we describe and comment on these findings, placing them in a broader context.
引用
收藏
页码:301 / 307
页数:7
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