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Histone H1 depletion in mammals alters global chromatin structure but causes specific changes in gene regulation.哺乳动物中组蛋白H1的缺失会改变整体染色质结构,但会导致基因调控发生特定变化。
Cell. 2005 Dec 29;123(7):1199-212. doi: 10.1016/j.cell.2005.10.028.
2
X-ray structure of a tetranucleosome and its implications for the chromatin fibre.四核小体的X射线结构及其对染色质纤维的影响。
Nature. 2005 Jul 7;436(7047):138-41. doi: 10.1038/nature03686.
3
A method for the in vitro reconstitution of a defined "30 nm" chromatin fibre containing stoichiometric amounts of the linker histone.一种用于体外重建含有化学计量的连接组蛋白的特定“30纳米”染色质纤维的方法。
J Mol Biol. 2005 Feb 4;345(5):957-68. doi: 10.1016/j.jmb.2004.10.075. Epub 2004 Dec 7.
4
Nucleosome arrays reveal the two-start organization of the chromatin fiber.核小体阵列揭示了染色质纤维的双起始结构。
Science. 2004 Nov 26;306(5701):1571-3. doi: 10.1126/science.1103124.
5
Linker histone-dependent organization and dynamics of nucleosome entry/exit DNAs.连接组蛋白依赖性核小体进出DNA的组织与动态变化
J Mol Biol. 2003 Aug 29;331(5):1025-40. doi: 10.1016/s0022-2836(03)00831-3.
6
Chromatin fiber folding: requirement for the histone H4 N-terminal tail.染色质纤维折叠:对组蛋白H4 N端尾部的需求
J Mol Biol. 2003 Mar 14;327(1):85-96. doi: 10.1016/s0022-2836(03)00025-1.
7
Structure of the yeast nucleosome core particle reveals fundamental changes in internucleosome interactions.酵母核小体核心颗粒的结构揭示了核小体间相互作用的根本变化。
EMBO J. 2001 Sep 17;20(18):5207-18. doi: 10.1093/emboj/20.18.5207.
8
The core histone N termini function independently of linker histones during chromatin condensation.在染色质凝聚过程中,核心组蛋白N端独立于连接组蛋白发挥作用。
J Biol Chem. 2000 Nov 24;275(47):37285-90. doi: 10.1074/jbc.M006801200.
9
DNase I digestion reveals alternating asymmetrical protection of the nucleosome by the higher order chromatin structure.脱氧核糖核酸酶I消化揭示了高阶染色质结构对核小体的交替不对称保护作用。
Nucleic Acids Res. 2000 Aug 15;28(16):3092-9. doi: 10.1093/nar/28.16.3092.
10
Physical constraints in the condensation of eukaryotic chromosomes. Local concentration of DNA versus linear packing ratio in higher order chromatin structures.真核染色体凝聚中的物理限制。高阶染色质结构中DNA的局部浓度与线性包装比。
Biochemistry. 2000 Apr 11;39(14):3861-6. doi: 10.1021/bi992628w.

电子显微镜测量确定了“30纳米”染色质纤维的尺寸:致密、相互交错结构的证据。

EM measurements define the dimensions of the "30-nm" chromatin fiber: evidence for a compact, interdigitated structure.

作者信息

Robinson Philip J J, Fairall Louise, Huynh Van A T, Rhodes Daniela

机构信息

Medical Research Council Laboratory of Molecular Biology, Hills Road, Cambridge CB2 2QH, United Kingdom.

出版信息

Proc Natl Acad Sci U S A. 2006 Apr 25;103(17):6506-11. doi: 10.1073/pnas.0601212103. Epub 2006 Apr 14.

DOI:10.1073/pnas.0601212103
PMID:16617109
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1436021/
Abstract

Chromatin structure plays a fundamental role in the regulation of nuclear processes such as DNA transcription, replication, recombination, and repair. Despite considerable efforts during three decades, the structure of the 30-nm chromatin fiber remains controversial. To define fiber dimensions accurately, we have produced very long and regularly folded 30-nm fibers from in vitro reconstituted nucleosome arrays containing the linker histone and with increasing nucleosome repeat lengths (10 to 70 bp of linker DNA). EM measurements show that the dimensions of these fully folded fibers do not increase linearly with increasing linker length, a finding that is inconsistent with two-start helix models. Instead, we find that there are two distinct classes of fiber structure, both with unexpectedly high nucleosome density: arrays with 10 to 40 bp of linker DNA all produce fibers with a diameter of 33 nm and 11 nucleosomes per 11 nm, whereas arrays with 50 to 70 bp of linker DNA all produce 44-nm-wide fibers with 15 nucleosomes per 11 nm. Using the physical constraints imposed by these measurements, we have built a model in which tight nucleosome packing is achieved through the interdigitation of nucleosomes from adjacent helical gyres. Importantly, the model closely matches raw image projections of folded chromatin arrays recorded in the solution state by using electron cryo-microscopy.

摘要

染色质结构在诸如DNA转录、复制、重组和修复等核过程的调控中起着基础性作用。尽管在三十年里付出了巨大努力,但30纳米染色质纤维的结构仍存在争议。为了准确确定纤维尺寸,我们从含有连接组蛋白且核小体重复长度不断增加(连接DNA为10至70碱基对)的体外重构核小体阵列中制备出了非常长且规则折叠的30纳米纤维。电子显微镜测量表明,这些完全折叠纤维的尺寸并不会随着连接长度的增加而呈线性增加,这一发现与双起始螺旋模型不一致。相反,我们发现存在两种不同类型的纤维结构,二者的核小体密度都出乎意料地高:连接DNA为10至40碱基对的阵列均产生直径为33纳米、每11纳米有11个核小体的纤维,而连接DNA为50至70碱基对的阵列均产生宽度为44纳米、每11纳米有15个核小体的纤维。利用这些测量所施加的物理限制,我们构建了一个模型,其中通过相邻螺旋回转的核小体相互交错实现了紧密的核小体堆积。重要的是,该模型与通过冷冻电子显微镜记录的溶液状态下折叠染色质阵列的原始图像投影紧密匹配。