• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Polycomb 系统的解耦进化和非典型 PRC1 的深远起源。

Uncoupled evolution of the Polycomb system and deep origin of non-canonical PRC1.

机构信息

Theoretical Biology and Bioinformatics, Department of Biology, Science Faculty, Utrecht University, Utrecht, Netherlands.

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

出版信息

Commun Biol. 2023 Nov 10;6(1):1144. doi: 10.1038/s42003-023-05501-x.

DOI:10.1038/s42003-023-05501-x
PMID:37949928
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10638273/
Abstract

Polycomb group proteins, as part of the Polycomb repressive complexes, are essential in gene repression through chromatin compaction by canonical PRC1, mono-ubiquitylation of histone H2A by non-canonical PRC1 and tri-methylation of histone H3K27 by PRC2. Despite prevalent models emphasizing tight functional coupling between PRC1 and PRC2, it remains unclear whether this paradigm indeed reflects the evolution and functioning of these complexes. Here, we conduct a comprehensive analysis of the presence or absence of cPRC1, nPRC1 and PRC2 across the entire eukaryotic tree of life, and find that both complexes were present in the Last Eukaryotic Common Ancestor (LECA). Strikingly, ~42% of organisms contain only PRC1 or PRC2, showing that their evolution since LECA is largely uncoupled. The identification of ncPRC1-defining subunits in unicellular relatives of animals and fungi suggests ncPRC1 originated before cPRC1, and we propose a scenario for the evolution of cPRC1 from ncPRC1. Together, our results suggest that crosstalk between these complexes is a secondary development in evolution.

摘要

多梳蛋白组蛋白作为多梳抑制复合物的一部分,通过经典的 PRC1 使染色质紧缩、非经典的 PRC1 使组蛋白 H2A 单泛素化以及 PRC2 使组蛋白 H3K27 三甲基化,从而在基因抑制中发挥重要作用。尽管普遍的模型强调 PRC1 和 PRC2 之间的紧密功能耦合,但尚不清楚这一范例是否确实反映了这些复合物的进化和功能。在这里,我们对整个真核生物进化树中 cPRC1、nPRC1 和 PRC2 的存在或缺失进行了全面分析,结果发现这两个复合物都存在于最后的真核生物共同祖先(LECA)中。引人注目的是,约 42%的生物只含有 PRC1 或 PRC2,表明自 LECA 以来它们的进化在很大程度上是不耦合的。在动物和真菌的单细胞亲属中鉴定出 ncPRC1 定义亚基表明 ncPRC1 起源于 cPRC1 之前,我们提出了 cPRC1 从 ncPRC1 进化而来的情景。总之,我们的研究结果表明,这些复合物之间的串扰是进化过程中的二次发育。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c93/10638273/36c73fd92647/42003_2023_5501_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c93/10638273/65427265c580/42003_2023_5501_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c93/10638273/559dfb5f9384/42003_2023_5501_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c93/10638273/d3fd68c2c2ea/42003_2023_5501_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c93/10638273/5893bd325c71/42003_2023_5501_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c93/10638273/25df084ad943/42003_2023_5501_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c93/10638273/db9c87a9d644/42003_2023_5501_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c93/10638273/36c73fd92647/42003_2023_5501_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c93/10638273/65427265c580/42003_2023_5501_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c93/10638273/559dfb5f9384/42003_2023_5501_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c93/10638273/d3fd68c2c2ea/42003_2023_5501_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c93/10638273/5893bd325c71/42003_2023_5501_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c93/10638273/25df084ad943/42003_2023_5501_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c93/10638273/db9c87a9d644/42003_2023_5501_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c93/10638273/36c73fd92647/42003_2023_5501_Fig7_HTML.jpg

相似文献

1
Uncoupled evolution of the Polycomb system and deep origin of non-canonical PRC1.Polycomb 系统的解耦进化和非典型 PRC1 的深远起源。
Commun Biol. 2023 Nov 10;6(1):1144. doi: 10.1038/s42003-023-05501-x.
2
PRC2.1- and PRC2.2-specific accessory proteins drive recruitment of different forms of canonical PRC1.PRC2.1 和 PRC2.2 特异性辅助蛋白驱动不同形式的经典 PRC1 的募集。
Mol Cell. 2023 May 4;83(9):1393-1411.e7. doi: 10.1016/j.molcel.2023.03.018. Epub 2023 Apr 7.
3
Interdependence of PRC1 and PRC2 for recruitment to Polycomb Response Elements.PRC1与PRC2在招募至多梳反应元件过程中的相互依赖性。
Nucleic Acids Res. 2016 Dec 1;44(21):10132-10149. doi: 10.1093/nar/gkw701. Epub 2016 Aug 23.
4
Goldilocks meets Polycomb.金发姑娘遇见 Polycomb。
Genes Dev. 2022 Oct 1;36(19-20):1043-1045. doi: 10.1101/gad.350248.122.
5
Functional redundancy among Polycomb complexes in maintaining the pluripotent state of embryonic stem cells.多梳复合物在维持胚胎干细胞多能性状态中的功能冗余。
Stem Cell Reports. 2022 May 10;17(5):1198-1214. doi: 10.1016/j.stemcr.2022.02.020. Epub 2022 Mar 31.
6
Polycomb-mediated histone modifications and gene regulation.多梳介导的组蛋白修饰和基因调控。
Biochem Soc Trans. 2024 Feb 28;52(1):151-161. doi: 10.1042/BST20230336.
7
Polycomb-dependent histone H2A ubiquitination links developmental disorders with cancer.多梳蛋白依赖性组蛋白H2A泛素化将发育障碍与癌症联系起来。
Trends Genet. 2022 Apr;38(4):333-352. doi: 10.1016/j.tig.2021.07.011. Epub 2021 Aug 20.
8
PR-DUB preserves Polycomb repression by preventing excessive accumulation of H2Aub1, an antagonist of chromatin compaction.PR-DUB 通过防止 H2Aub1 的过度积累来维持 Polycomb 抑制,H2Aub1 是染色质紧缩的拮抗剂。
Genes Dev. 2022 Oct 1;36(19-20):1046-1061. doi: 10.1101/gad.350014.122. Epub 2022 Nov 10.
9
Jarid2 binds mono-ubiquitylated H2A lysine 119 to mediate crosstalk between Polycomb complexes PRC1 and PRC2.Jarid2 结合单泛素化 H2A 赖氨酸 119 以介导多梳复合物 PRC1 和 PRC2 之间的串扰。
Nat Commun. 2016 Nov 28;7:13661. doi: 10.1038/ncomms13661.
10
H2A monoubiquitination in Arabidopsis thaliana is generally independent of LHP1 and PRC2 activity.拟南芥中的H2A单泛素化通常独立于LHP1和PRC2活性。
Genome Biol. 2017 Apr 12;18(1):69. doi: 10.1186/s13059-017-1197-z.

引用本文的文献

1
Aere perennius: how chromatin fidelity is maintained and lost in disease.经久不衰:疾病中染色质保真度是如何维持和丧失的
NAR Mol Med. 2025 Jul 22;2(3):ugaf026. doi: 10.1093/narmme/ugaf026. eCollection 2025 Jul.
2
Repressive Cytosine Methylation is a Marker of Viral Gene Transfer Across Divergent Eukaryotes.抑制性胞嘧啶甲基化是病毒基因在不同真核生物间转移的一个标志。
Mol Biol Evol. 2025 Jul 30;42(8). doi: 10.1093/molbev/msaf176.
3
Hao-Fountain syndrome protein USP7 controls neuronal differentiation via BCOR-ncPRC1.1.郝-方丹综合征蛋白USP7通过BCOR-ncPRC1.1控制神经元分化。

本文引用的文献

1
The Polycomb repressive complex 2 deposits H3K27me3 and represses transposable elements in a broad range of eukaryotes.多梳抑制复合物 2 沉积 H3K27me3 并在广泛的真核生物中抑制转座元件。
Curr Biol. 2023 Oct 23;33(20):4367-4380.e9. doi: 10.1016/j.cub.2023.08.073. Epub 2023 Sep 21.
2
Cohesin contributes to transcriptional repression of stage-specific genes in the human malaria parasite.黏连蛋白有助于人类疟原虫中阶段特异性基因的转录抑制。
EMBO Rep. 2023 Oct 9;24(10):e57090. doi: 10.15252/embr.202357090. Epub 2023 Aug 18.
3
PR-DUB preserves Polycomb repression by preventing excessive accumulation of H2Aub1, an antagonist of chromatin compaction.
Genes Dev. 2025 Mar 3;39(5-6):401-422. doi: 10.1101/gad.352272.124.
4
Targeting chromatin modifying complexes in acute myeloid leukemia.靶向急性髓系白血病中的染色质修饰复合物
Stem Cells Transl Med. 2025 Feb 11;14(2). doi: 10.1093/stcltm/szae089.
5
On the possibility of yet a third kinetochore system in the protist phylum Euglenozoa.关于原生生物门眼虫纲中可能存在第三种动粒系统的探讨。
mBio. 2024 Dec 11;15(12):e0293624. doi: 10.1128/mbio.02936-24. Epub 2024 Oct 30.
6
Sustained inactivation of the Polycomb PRC1 complex induces DNA repair defects and genomic instability in epigenetic tumors.持续失活的多梳 PRC1 复合物在表观遗传学肿瘤中诱导 DNA 修复缺陷和基因组不稳定性。
Histochem Cell Biol. 2024 Jul;162(1-2):133-147. doi: 10.1007/s00418-024-02302-z. Epub 2024 Jun 18.
7
Kinetoplastid kinetochore proteins KKT14-KKT15 are divergent Bub1/BubR1-Bub3 proteins.动基体类动粒蛋白 KKT14-KKT15 是有差异的 Bub1/BubR1-Bub3 蛋白。
Open Biol. 2024 Jun;14(6):240025. doi: 10.1098/rsob.240025. Epub 2024 Jun 12.
8
Chromatin profiling identifies putative dual roles for H3K27me3 in regulating transposons and cell type-specific genes in choanoflagellates.染色质分析揭示了H3K27me3在调节领鞭毛虫转座子和细胞类型特异性基因方面可能具有的双重作用。
bioRxiv. 2024 May 30:2024.05.28.596151. doi: 10.1101/2024.05.28.596151.
9
Sustained inactivation of the Polycomb PRC1 complex induces DNA repair defects and genomic instability in epigenetic tumors.多梳PRC1复合物的持续失活会在表观遗传肿瘤中诱导DNA修复缺陷和基因组不稳定。
Res Sq. 2024 Apr 24:rs.3.rs-4289524. doi: 10.21203/rs.3.rs-4289524/v1.
10
Research advances of polycomb group proteins in regulating mammalian development.多梳蛋白家族在调控哺乳动物发育中的研究进展
Front Cell Dev Biol. 2024 Mar 5;12:1383200. doi: 10.3389/fcell.2024.1383200. eCollection 2024.
PR-DUB 通过防止 H2Aub1 的过度积累来维持 Polycomb 抑制,H2Aub1 是染色质紧缩的拮抗剂。
Genes Dev. 2022 Oct 1;36(19-20):1046-1061. doi: 10.1101/gad.350014.122. Epub 2022 Nov 10.
4
USP7 regulates the ncPRC1 Polycomb axis to stimulate genomic H2AK119ub1 deposition uncoupled from H3K27me3.USP7调节ncPRC1多梳轴,以刺激与H3K27me3解偶联的基因组H2AK119ub1沉积。
Sci Adv. 2022 Nov 4;8(44):eabq7598. doi: 10.1126/sciadv.abq7598.
5
Variant Polycomb complexes in consistent with ancient functional diversity.变异的多梳蛋白复合体与古老的功能多样性相一致。
Sci Adv. 2022 Sep 9;8(36):eadd0103. doi: 10.1126/sciadv.add0103. Epub 2022 Sep 7.
6
A small RNA-guided PRC2 complex eliminates DNA as an extreme form of transposon silencing.一个小 RNA 引导的 PRC2 复合物消除了 DNA 作为转座子沉默的极端形式。
Cell Rep. 2022 Aug 23;40(8):111263. doi: 10.1016/j.celrep.2022.111263.
7
MES-3 is a highly divergent ortholog of the canonical PRC2 component SUZ12.MES-3是典型的PRC2组件SUZ12的一个高度分化的直系同源物。
iScience. 2022 Jun 17;25(7):104633. doi: 10.1016/j.isci.2022.104633. eCollection 2022 Jul 15.
8
Context-specific Polycomb mechanisms in development.发育过程中具有特定背景的 Polycomb 机制。
Nat Rev Genet. 2022 Nov;23(11):680-695. doi: 10.1038/s41576-022-00499-0. Epub 2022 Jun 9.
9
A phylogenetic and proteomic reconstruction of eukaryotic chromatin evolution.真核染色质进化的系统发育和蛋白质组重建。
Nat Ecol Evol. 2022 Jul;6(7):1007-1023. doi: 10.1038/s41559-022-01771-6. Epub 2022 Jun 9.
10
Histone editing elucidates the functional roles of H3K27 methylation and acetylation in mammals.组蛋白编辑阐明了 H3K27 甲基化和乙酰化在哺乳动物中的功能作用。
Nat Genet. 2022 Jun;54(6):754-760. doi: 10.1038/s41588-022-01091-2. Epub 2022 Jun 6.