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人工染色体与启动表观遗传着丝粒建立的策略

Artificial Chromosomes and Strategies to Initiate Epigenetic Centromere Establishment.

作者信息

Barrey Evelyne J, Heun Patrick

机构信息

Wellcome Trust Centre for Cell Biology, The University of Edinburgh, Edinburgh, UK.

出版信息

Prog Mol Subcell Biol. 2017;56:193-212. doi: 10.1007/978-3-319-58592-5_8.

DOI:10.1007/978-3-319-58592-5_8
PMID:28840238
Abstract

In recent years, various synthetic approaches have been developed to address the question of what directs centromere establishment and maintenance. In this chapter, we will discuss how approaches aimed at constructing synthetic centromeres have co-evolved with and contributed to shape the theory describing the determinants of centromere identity. We will first review lessons learned from artificial chromosomes created from "naked" centromeric sequences to investigate the role of the underlying DNA for centromere formation. We will then discuss how several studies, which applied removal of endogenous centromeres or over-expression of the centromere-specific histone CENP-A, helped to investigate the contribution of chromatin context to centromere establishment. Finally, we will examine various biosynthetic approaches taking advantage of targeting specific proteins to ectopic sites in the genome to dissect the role of many centromere-associated proteins and chromatin modifiers for centromere inheritance and function. Together, these studies showed that chromatin context matters, particularly proximity to heterochromatin or repetitive DNA sequences. Moreover, despite the important contribution of centromeric DNA, the centromere-specific histone H3-variant CENP-A emerges as a key epigenetic mark to establish and maintain functional centromeres on artificial chromosomes or at ectopic sites of the genome.

摘要

近年来,人们开发了各种合成方法来解决是什么指导着着丝粒的建立和维持这一问题。在本章中,我们将讨论旨在构建合成着丝粒的方法是如何与描述着丝粒身份决定因素的理论共同发展并对其形成做出贡献的。我们将首先回顾从由“裸”着丝粒序列创建的人工染色体中获得的经验教训,以研究基础DNA在着丝粒形成中的作用。然后,我们将讨论几项研究,这些研究通过去除内源性着丝粒或过表达着丝粒特异性组蛋白CENP-A,有助于研究染色质环境对着丝粒建立的贡献。最后,我们将研究利用将特定蛋白质靶向基因组异位位点的各种生物合成方法,以剖析许多着丝粒相关蛋白质和染色质修饰剂在着丝粒遗传和功能中的作用。这些研究共同表明,染色质环境很重要,特别是与异染色质或重复DNA序列的接近程度。此外,尽管着丝粒DNA有重要贡献,但着丝粒特异性组蛋白H3变体CENP-A作为一种关键的表观遗传标记出现,用于在人工染色体上或基因组的异位位点建立和维持功能性着丝粒。

相似文献

1
Artificial Chromosomes and Strategies to Initiate Epigenetic Centromere Establishment.人工染色体与启动表观遗传着丝粒建立的策略
Prog Mol Subcell Biol. 2017;56:193-212. doi: 10.1007/978-3-319-58592-5_8.
2
"Lessons from the extremes: Epigenetic and genetic regulation in point monocentromere and holocentromere establishment on artificial chromosomes".“极端情况下的启示:人工染色体上的点着丝粒和全着丝粒建立的表观遗传和遗传调控”。
Exp Cell Res. 2020 May 15;390(2):111974. doi: 10.1016/j.yexcr.2020.111974. Epub 2020 Mar 26.
3
DNA Sequences in Centromere Formation and Function.着丝粒形成与功能中的DNA序列
Prog Mol Subcell Biol. 2017;56:305-336. doi: 10.1007/978-3-319-58592-5_13.
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Quantitative Microscopy Reveals Centromeric Chromatin Stability, Size, and Cell Cycle Mechanisms to Maintain Centromere Homeostasis.定量显微镜揭示着丝粒染色质稳定性、大小及维持着丝粒稳态的细胞周期机制。
Prog Mol Subcell Biol. 2017;56:139-162. doi: 10.1007/978-3-319-58592-5_6.
5
Histone H3K9 and H4 Acetylations and Transcription Facilitate the Initial CENP-A Deposition and De Novo Centromere Establishment in Caenorhabditis elegans Artificial Chromosomes.组蛋白 H3K9 和 H4 的乙酰化作用以及转录促进了秀丽隐杆线虫人工染色体中 CENP-A 的初始沉积和从头建立新的着丝粒。
Epigenetics Chromatin. 2018 Apr 13;11(1):16. doi: 10.1186/s13072-018-0185-1.
6
Genetic and epigenetic effects on centromere establishment.遗传和表观遗传对着丝粒建立的影响。
Chromosoma. 2020 Mar;129(1):1-24. doi: 10.1007/s00412-019-00727-3. Epub 2019 Nov 28.
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Centromeric and ectopic assembly of CENP-A chromatin in health and cancer: old marks and new tracks.着丝粒和 CENP-A 染色质的异位组装在健康和癌症中的作用:旧标记和新轨迹。
Nucleic Acids Res. 2019 Feb 20;47(3):1051-1069. doi: 10.1093/nar/gky1298.
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Sequence features and transcriptional stalling within centromere DNA promote establishment of CENP-A chromatin.着丝粒 DNA 中的序列特征和转录停滞促进 CENP-A 染色质的建立。
PLoS Genet. 2015 Mar 4;11(3):e1004986. doi: 10.1371/journal.pgen.1004986. eCollection 2015 Mar.
9
Genetic and epigenetic regulation of centromeres: a look at HAC formation.着丝粒的遗传与表观遗传调控:审视人类人工染色体的形成
Chromosome Res. 2015 Feb;23(1):87-103. doi: 10.1007/s10577-015-9470-z.
10
CENP-A chromatin prevents replication stress at centromeres to avoid structural aneuploidy.着丝粒 CENP-A 染色质可防止着丝粒处的复制应激,从而避免结构非整倍体。
Proc Natl Acad Sci U S A. 2021 Mar 9;118(10). doi: 10.1073/pnas.2015634118.

引用本文的文献

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Efficient formation of single-copy human artificial chromosomes.高效构建单拷贝人源人工染色体。
Science. 2024 Mar 22;383(6689):1344-1349. doi: 10.1126/science.adj3566. Epub 2024 Mar 21.
2
Centromere structure and function: lessons from Drosophila.着丝粒结构与功能:来自果蝇的启示。
Genetics. 2023 Dec 6;225(4). doi: 10.1093/genetics/iyad170.
3
The unique kind of human artificial chromosome: Bypassing the requirement for repetitive centromere DNA.独特的人类人工染色体:绕过对重复着丝粒 DNA 的需求。
Exp Cell Res. 2020 Jun 15;391(2):111978. doi: 10.1016/j.yexcr.2020.111978. Epub 2020 Apr 1.
4
Genetic and epigenetic effects on centromere establishment.遗传和表观遗传对着丝粒建立的影响。
Chromosoma. 2020 Mar;129(1):1-24. doi: 10.1007/s00412-019-00727-3. Epub 2019 Nov 28.
5
Human Artificial Chromosomes that Bypass Centromeric DNA.人类人工染色体,绕过着丝粒 DNA。
Cell. 2019 Jul 25;178(3):624-639.e19. doi: 10.1016/j.cell.2019.06.006.
6
Fork pausing allows centromere DNA loop formation and kinetochore assembly.着丝粒 DNA 环形成和动粒装配允许叉暂停。
Proc Natl Acad Sci U S A. 2018 Nov 13;115(46):11784-11789. doi: 10.1073/pnas.1806791115. Epub 2018 Oct 29.
7
The cellular mechanisms and consequences of centromere drive.着丝粒驱动的细胞机制和后果。
Curr Opin Cell Biol. 2018 Jun;52:58-65. doi: 10.1016/j.ceb.2018.01.011. Epub 2018 Feb 16.