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脊椎动物着丝粒结构:从染色质丝到功能结构。

Vertebrate centromere architecture: from chromatin threads to functional structures.

机构信息

Hubrecht Institute, Royal Netherlands Academy of Arts and Sciences, Utrecht, Netherlands.

University Medical Center Utrecht, Utrecht, Netherlands.

出版信息

Chromosoma. 2024 Jul;133(3):169-181. doi: 10.1007/s00412-024-00823-z. Epub 2024 Jun 10.

DOI:10.1007/s00412-024-00823-z
PMID:38856923
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11266386/
Abstract

Centromeres are chromatin structures specialized in sister chromatid cohesion, kinetochore assembly, and microtubule attachment during chromosome segregation. The regional centromere of vertebrates consists of long regions of highly repetitive sequences occupied by the Histone H3 variant CENP-A, and which are flanked by pericentromeres. The three-dimensional organization of centromeric chromatin is paramount for its functionality and its ability to withstand spindle forces. Alongside CENP-A, key contributors to the folding of this structure include components of the Constitutive Centromere-Associated Network (CCAN), the protein CENP-B, and condensin and cohesin complexes. Despite its importance, the intricate architecture of the regional centromere of vertebrates remains largely unknown. Recent advancements in long-read sequencing, super-resolution and cryo-electron microscopy, and chromosome conformation capture techniques have significantly improved our understanding of this structure at various levels, from the linear arrangement of centromeric sequences and their epigenetic landscape to their higher-order compaction. In this review, we discuss the latest insights on centromere organization and place them in the context of recent findings describing a bipartite higher-order organization of the centromere.

摘要

着丝粒是一种专门的染色质结构,在有丝分裂过程中负责姐妹染色单体的黏合、动粒的组装和微管的附着。脊椎动物的区域着丝粒由富含高度重复序列的长区域组成,这些区域被组蛋白 H3 变体 CENP-A 占据,其两侧为着丝粒周围区。着丝粒染色质的三维结构对于其功能和承受纺锤体力的能力至关重要。除了 CENP-A 之外,对这种结构折叠的关键贡献者还包括组成组成型着丝粒相关网络(CCAN)的成分、蛋白 CENP-B 以及凝缩素和黏合素复合物。尽管其重要性,脊椎动物区域着丝粒的复杂结构在很大程度上仍未知。长读测序、超分辨率和冷冻电镜以及染色体构象捕获技术的最新进展极大地提高了我们对该结构在各个层面的理解,从着丝粒序列的线性排列及其表观遗传景观到它们的高级压缩。在这篇综述中,我们讨论了关于着丝粒组织的最新见解,并将它们置于描述着丝粒二分体高级组织的最新发现的背景下。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa2e/11266386/b91539ec22f7/412_2024_823_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa2e/11266386/3d6a5b61bb7d/412_2024_823_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa2e/11266386/f34c692c915c/412_2024_823_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa2e/11266386/b91539ec22f7/412_2024_823_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa2e/11266386/3d6a5b61bb7d/412_2024_823_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa2e/11266386/f34c692c915c/412_2024_823_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa2e/11266386/b91539ec22f7/412_2024_823_Fig3_HTML.jpg

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引用本文的文献

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A chromatin-remodeling-independent role for ATRX in protecting centromeric cohesion.ATRX在保护着丝粒黏连中具有不依赖于染色质重塑的作用。

本文引用的文献

1
Vertebrate centromeres in mitosis are functionally bipartite structures stabilized by cohesin.脊椎动物有丝分裂着丝粒是由黏合蛋白稳定的功能二分体结构。
Cell. 2024 Jun 6;187(12):3006-3023.e26. doi: 10.1016/j.cell.2024.04.014. Epub 2024 May 13.
2
A non-canonical role of the inner kinetochore in regulating sister-chromatid cohesion at centromeres.内着丝粒在调节着丝粒处姐妹染色单体黏合的非规范作用。
EMBO J. 2024 Jun;43(12):2424-2452. doi: 10.1038/s44318-024-00104-6. Epub 2024 May 7.
3
The variation and evolution of complete human centromeres.
EMBO J. 2025 May 28. doi: 10.1038/s44318-025-00465-6.
人类完整着丝粒的变异与进化。
Nature. 2024 May;629(8010):136-145. doi: 10.1038/s41586-024-07278-3. Epub 2024 Apr 3.
4
CENP-A and CENP-B collaborate to create an open centromeric chromatin state.着丝粒蛋白 A 和着丝粒蛋白 B 协作形成开放的着丝粒染色质状态。
Nat Commun. 2023 Dec 12;14(1):8227. doi: 10.1038/s41467-023-43739-5.
5
Defining a core configuration for human centromeres during mitosis.定义有丝分裂过程中人着丝粒的核心结构。
Nat Commun. 2023 Dec 1;14(1):7947. doi: 10.1038/s41467-023-42980-2.
6
Condensin dysfunction is a reproductive isolating barrier in mice.凝聚素功能障碍是小鼠生殖隔离的屏障。
Nature. 2023 Nov;623(7986):347-355. doi: 10.1038/s41586-023-06700-6. Epub 2023 Nov 1.
7
Single molecule analysis of CENP-A chromatin by high-speed atomic force microscopy.高速原子力显微镜对 CENP-A 染色质的单分子分析。
Elife. 2023 Sep 20;12:e86709. doi: 10.7554/eLife.86709.
8
Centromere/kinetochore is assembled through CENP-C oligomerization.着丝粒/动粒通过CENP-C寡聚化组装而成。
Mol Cell. 2023 Jul 6;83(13):2188-2205.e13. doi: 10.1016/j.molcel.2023.05.023. Epub 2023 Jun 8.
9
Genome control by SMC complexes.SMC 复合物的基因组控制。
Nat Rev Mol Cell Biol. 2023 Sep;24(9):633-650. doi: 10.1038/s41580-023-00609-8. Epub 2023 May 25.
10
Visualization of the three-dimensional structure of the human centromere in mitotic chromosomes by superresolution microscopy.利用超分辨率显微镜对有丝分裂染色体中人类着丝粒的三维结构进行可视化。
Mol Biol Cell. 2023 May 15;34(6):ar61. doi: 10.1091/mbc.E22-08-0332. Epub 2023 Mar 22.