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着丝粒促成艰难的交易。

Centromeres Drive a Hard Bargain.

作者信息

Rosin Leah F, Mellone Barbara G

机构信息

Department of Molecular and Cell Biology, University of Connecticut, Storrs, CT 06269, USA; Current address: Department of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.

Department of Molecular and Cell Biology, University of Connecticut, Storrs, CT 06269, USA; Institute for Systems Genomics, University of Connecticut, Storrs, CT 06269, USA.

出版信息

Trends Genet. 2017 Feb;33(2):101-117. doi: 10.1016/j.tig.2016.12.001. Epub 2017 Jan 7.

DOI:10.1016/j.tig.2016.12.001
PMID:28069312
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5467322/
Abstract

Centromeres are essential chromosomal structures that mediate the accurate distribution of genetic material during meiotic and mitotic cell divisions. In most organisms, centromeres are epigenetically specified and propagated by nucleosomes containing the centromere-specific H3 variant, centromere protein A (CENP-A). Although centromeres perform a critical and conserved function, CENP-A and the underlying centromeric DNA are rapidly evolving. This paradox has been explained by the centromere drive hypothesis, which proposes that CENP-A is undergoing an evolutionary tug-of-war with selfish centromeric DNA. Here, we review our current understanding of CENP-A evolution in relation to centromere drive and discuss classical and recent advances, including new evidence implicating CENP-A chaperones in this conflict.

摘要

着丝粒是重要的染色体结构,在减数分裂和有丝分裂细胞分裂过程中介导遗传物质的准确分配。在大多数生物体中,着丝粒是由含有着丝粒特异性H3变体——着丝粒蛋白A(CENP-A)的核小体在表观遗传上指定和传递的。尽管着丝粒执行着关键且保守的功能,但CENP-A和潜在的着丝粒DNA却在快速进化。着丝粒驱动假说来解释了这一矛盾,该假说提出CENP-A正在与自私的着丝粒DNA进行一场进化拔河比赛。在这里,我们回顾了目前对与着丝粒驱动相关的CENP-A进化的理解,并讨论了经典和最新进展,包括暗示CENP-A伴侣蛋白参与这场冲突的新证据。

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Centromeres Drive a Hard Bargain.着丝粒促成艰难的交易。
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2
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Spindle checkpoint can secure additional cheating time for selfish expanded centromeres.纺锤体检查点可以为自私扩展的着丝粒确保额外的作弊时间。
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Adaptive evolution of CENP-T modulates centromere binding.CENP-T的适应性进化调节着着丝粒结合。

本文引用的文献

1
CenH3 evolution reflects meiotic symmetry as predicted by the centromere drive model.CenH3 的进化反映了减数分裂对称,正如着丝粒驱动模型所预测的那样。
Sci Rep. 2016 Sep 15;6:33308. doi: 10.1038/srep33308.
2
Absence of positive selection on CenH3 in Luzula suggests that holokinetic chromosomes may suppress centromere drive.在灯心草属中,CenH3缺乏正向选择表明全动染色体可能抑制着丝粒驱动。
Ann Bot. 2016 Dec;118(7):1347-1352. doi: 10.1093/aob/mcw186. Epub 2016 Sep 10.
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Human centromere repositioning within euchromatin after partial chromosome deletion.
Curr Biol. 2025 Mar 10;35(5):1012-1022.e5. doi: 10.1016/j.cub.2025.01.017. Epub 2025 Feb 12.
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Centromere drive may propel the evolution of chromosome and genome size in plants.着丝粒驱动可能推动植物染色体和基因组大小的进化。
Ann Bot. 2024 Dec 31;134(6):1067-1076. doi: 10.1093/aob/mcae149.
5
Investigation of differentially expressed genes related to cellular senescence between high-risk and non-high-risk groups in neuroblastoma.神经母细胞瘤高危组与非高危组中细胞衰老相关差异表达基因的研究
Front Cell Dev Biol. 2024 Jul 29;12:1421673. doi: 10.3389/fcell.2024.1421673. eCollection 2024.
6
Meiosis-specific decoupling of the pericentromere from the kinetochore.减数分裂过程中着丝粒与动粒在着丝粒周围区域的特异性解偶联。
bioRxiv. 2024 Jul 22:2024.07.21.604490. doi: 10.1101/2024.07.21.604490.
7
An egg-sabotaging mechanism drives non-Mendelian transmission in mice.一种破坏卵子的机制驱动了小鼠的非孟德尔遗传。
Curr Biol. 2024 Sep 9;34(17):3845-3854.e4. doi: 10.1016/j.cub.2024.07.001. Epub 2024 Jul 26.
8
An egg sabotaging mechanism drives non-Mendelian transmission in mice.一种卵子破坏机制驱动小鼠中的非孟德尔遗传传递。
bioRxiv. 2024 Feb 23:2024.02.22.581453. doi: 10.1101/2024.02.22.581453.
9
Genome-wide analysis reveals the contributors to fast molecular evolution of the Chinese hook snout carp ().全基因组分析揭示了中华倒刺鲃快速分子进化的影响因素。
Comput Struct Biotechnol J. 2024 May 31;23:2465-2477. doi: 10.1016/j.csbj.2024.05.048. eCollection 2024 Dec.
10
The Chaperone NASP Contributes to de Novo Deposition of the Centromeric Histone Variant CENH3 in Arabidopsis Early Embryogenesis.伴侣蛋白 NASP 有助于中心体组蛋白变体 CENH3 在拟南芥早期胚胎发生中的从头沉积。
Plant Cell Physiol. 2024 Jul 30;65(7):1135-1148. doi: 10.1093/pcp/pcae030.
部分染色体缺失后人类着丝粒在常染色质内的重新定位。
Chromosome Res. 2016 Dec;24(4):451-466. doi: 10.1007/s10577-016-9536-6. Epub 2016 Aug 31.
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Centromere inactivation on a neo-Y fusion chromosome in threespine stickleback fish.三刺鱼新Y融合染色体上的着丝粒失活
Chromosome Res. 2016 Dec;24(4):437-450. doi: 10.1007/s10577-016-9535-7. Epub 2016 Aug 23.
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Genomic variation within alpha satellite DNA influences centromere location on human chromosomes with metastable epialleles.α卫星DNA内的基因组变异通过亚稳定表观等位基因影响人类染色体上的着丝粒位置。
Genome Res. 2016 Oct;26(10):1301-1311. doi: 10.1101/gr.206706.116. Epub 2016 Aug 10.
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Chromatin assembly: Journey to the CENter of the chromosome.染色质组装:迈向染色体中心的旅程。
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