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着丝粒的表观遗传继承

Epigenetic inheritance of centromeres.

作者信息

Henikoff S, Furuyama T

机构信息

Howard Hughes Medical Institute, Fred Hutchinson Cancer Research Center, Seattle, Washington 98109, USA.

出版信息

Cold Spring Harb Symp Quant Biol. 2010;75:51-60. doi: 10.1101/sqb.2010.75.001. Epub 2010 Nov 3.

DOI:10.1101/sqb.2010.75.001
PMID:21047902
Abstract

Centromeres of higher eukaryotes are epigenetically maintained; however, the mechanism that underlies centromere inheritance is unknown. Centromere identity and inheritance require the assembly of nucleosomes containing the CenH3 histone variant in place of canonical H3. Work from our laboratory has led to the proposal that epigenetic inheritance of centromeres evolved as adaptations of CenH3 and other centromere proteins to resist drive of selfish centromeres during female meiosis. Our molecular studies have revealed that the Drosophila CenH3 nucleosome is equivalent to half of the canonical H3 nucleosome and induces positive supercoils, as opposed to the negative supercoils induced by an H3 nucleosome. CenH3 likewise induces positive supercoils in functional yeast centromeres in vivo. The right-handed wrapping of DNA around the histone core implied by positive supercoiling indicates that centromeric nucleosomes are unlikely to be octameric and that the exposed surfaces holding the nucleosome together would be available for kinetochore protein recruitment. The mutual incompatibility of nucleosomes with opposite topologies could explain how centromeres are efficiently maintained as unique loci on chromosomes. We propose that the opposite wrapping of DNA around a half-nucleosome core particle facilitates a mode of inheritance that does not depend on DNA sequence, DNA modification or protein conformation.

摘要

高等真核生物的着丝粒通过表观遗传得以维持;然而,着丝粒遗传的潜在机制尚不清楚。着丝粒的身份和遗传需要组装含有CenH3组蛋白变体而非经典H3的核小体。我们实验室的研究提出,着丝粒的表观遗传是CenH3和其他着丝粒蛋白在雌性减数分裂过程中为抵抗自私着丝粒的驱动而进化出的适应性特征。我们的分子研究表明,果蝇的CenH3核小体相当于经典H3核小体的一半,并诱导正超螺旋,而H3核小体诱导负超螺旋。同样,CenH3在体内功能性酵母着丝粒中也诱导正超螺旋。正超螺旋所暗示的DNA围绕组蛋白核心的右手缠绕表明,着丝粒核小体不太可能是八聚体,并且将核小体结合在一起的暴露表面可用于动粒蛋白的募集。具有相反拓扑结构的核小体之间的相互不相容性可以解释着丝粒如何作为染色体上独特的位点有效地维持。我们提出,DNA围绕半核小体核心颗粒的相反缠绕促进了一种不依赖于DNA序列、DNA修饰或蛋白质构象的遗传模式。

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Epigenetic inheritance of centromeres.着丝粒的表观遗传继承
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