• 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

染色质对HIV-1整合、转录和潜伏的多方面贡献。

The Multifaceted Contributions of Chromatin to HIV-1 Integration, Transcription, and Latency.

作者信息

De Crignis E, Mahmoudi T

机构信息

Department of Biochemistry, Erasmus University Medical Centre , Rotterdam , The Netherlands.

Department of Biochemistry, Erasmus University Medical Centre , Rotterdam , The Netherlands.

出版信息

Int Rev Cell Mol Biol. 2017;328:197-252. doi: 10.1016/bs.ircmb.2016.08.006. Epub 2016 Oct 5.

DOI:10.1016/bs.ircmb.2016.08.006
PMID:28069134
Abstract

The capacity of the human immunodeficiency virus (HIV-1) to establish latent infections constitutes a major barrier to the development of a cure for HIV-1. In latent infection, replication competent HIV-1 provirus is integrated within the host genome but remains silent, masking the infected cells from the activity of the host immune response. Despite the progress in elucidating the molecular players that regulate HIV-1 gene expression, the mechanisms driving the establishment and maintenance of latency are still not fully understood. Transcription from the HIV-1 genome occurs in the context of chromatin and is subjected to the same regulatory mechanisms that drive cellular gene expression. Much like in eukaryotic genes, the nucleosomal landscape of the HIV-1 promoter and its position within genomic chromatin are determinants of its transcriptional activity. Understanding the multilayered chromatin-mediated mechanisms that underpin HIV-1 integration and expression is of utmost importance for the development of therapeutic strategies aimed at reducing the pool of latently infected cells. In this review, we discuss the impact of chromatin structure on viral integration, transcriptional regulation and latency, and the host factors that influence HIV-1 replication by regulating chromatin organization. Finally, we describe therapeutic strategies under development to target the chromatin-HIV-1 interplay.

摘要

人类免疫缺陷病毒1型(HIV-1)建立潜伏感染的能力是研发HIV-1治愈方法的主要障碍。在潜伏感染中,具有复制能力的HIV-1前病毒整合在宿主基因组中,但保持沉默,使受感染细胞免受宿主免疫反应的作用。尽管在阐明调控HIV-1基因表达的分子因素方面取得了进展,但驱动潜伏建立和维持的机制仍未完全了解。HIV-1基因组的转录发生在染色质环境中,并受到驱动细胞基因表达的相同调控机制的影响。与真核基因非常相似,HIV-1启动子的核小体格局及其在基因组染色质中的位置是其转录活性的决定因素。了解支撑HIV-1整合和表达的多层染色质介导机制对于开发旨在减少潜伏感染细胞库的治疗策略至关重要。在本综述中,我们讨论了染色质结构对病毒整合、转录调控和潜伏的影响,以及通过调节染色质组织影响HIV-1复制的宿主因素。最后,我们描述了正在开发的针对染色质与HIV-1相互作用的治疗策略。

相似文献

1
The Multifaceted Contributions of Chromatin to HIV-1 Integration, Transcription, and Latency.染色质对HIV-1整合、转录和潜伏的多方面贡献。
Int Rev Cell Mol Biol. 2017;328:197-252. doi: 10.1016/bs.ircmb.2016.08.006. Epub 2016 Oct 5.
2
Chromatin-associated regulation of HIV-1 transcription: implications for the development of therapeutic strategies.HIV-1转录的染色质相关调控:对治疗策略开发的启示
Subcell Biochem. 2007;41:371-96.
3
Underlying mechanisms of HIV-1 latency.HIV-1潜伏的潜在机制。
Virus Genes. 2017 Jun;53(3):329-339. doi: 10.1007/s11262-017-1443-1. Epub 2017 Mar 3.
4
HIV Provirus Stably Reproduces Parental Latent and Induced Transcription Phenotypes Regardless of the Chromosomal Integration Site.无论染色体整合位点如何,HIV前病毒都能稳定地重现亲本的潜伏和诱导转录表型。
J Virol. 2016 May 12;90(11):5302-14. doi: 10.1128/JVI.02842-15. Print 2016 Jun 1.
5
Anti-viral opportunities during transcriptional activation of latent HIV in the host chromatin.在宿主染色质中潜伏 HIV 的转录激活过程中的抗病毒机会。
Methods. 2011 Jan;53(1):97-101. doi: 10.1016/j.ymeth.2010.09.001. Epub 2010 Sep 7.
6
The Molecular Biology of HIV Latency.HIV 潜伏期的分子生物学
Adv Exp Med Biol. 2018;1075:187-212. doi: 10.1007/978-981-13-0484-2_8.
7
Connecting HIV-1 integration and transcription: a step toward new treatments.连接HIV-1整合与转录:迈向新疗法的一步。
FEBS Lett. 2016 Jul;590(13):1927-39. doi: 10.1002/1873-3468.12226. Epub 2016 Jun 16.
8
Human immunodeficiency virus (HIV)-1 integration sites in viral latency.病毒潜伏状态下的人类免疫缺陷病毒1型(HIV-1)整合位点
Curr HIV/AIDS Rep. 2015 Mar;12(1):88-96. doi: 10.1007/s11904-014-0241-9.
9
HIV Latency Gets a New Histone Mark.HIV潜伏获得新的组蛋白标记。
Cell Host Microbe. 2017 May 10;21(5):549-550. doi: 10.1016/j.chom.2017.04.012.
10
Suv39H1 and HP1gamma are responsible for chromatin-mediated HIV-1 transcriptional silencing and post-integration latency.Suv39H1和HP1γ负责染色质介导的HIV-1转录沉默和整合后潜伏期。
EMBO J. 2007 Jan 24;26(2):424-35. doi: 10.1038/sj.emboj.7601517.

引用本文的文献

1
FUBP3: A new player in HIV-1 transcriptional activation and immune regulation.FUBP3:HIV-1转录激活和免疫调节中的新角色。
Mol Ther Nucleic Acids. 2025 May 27;36(2):102565. doi: 10.1016/j.omtn.2025.102565. eCollection 2025 Jun 10.
2
Inducible cell lines producing replication-defective human immunodeficiency virus particles containing envelope glycoproteins stabilized in a pretriggered conformation.可诱导细胞系产生含有以预触发构象稳定化的包膜糖蛋白的复制缺陷型人类免疫缺陷病毒颗粒。
J Virol. 2024 Dec 17;98(12):e0172024. doi: 10.1128/jvi.01720-24. Epub 2024 Nov 7.
3
HIV-Tocky system to visualize proviral expression dynamics.
HIV-Tock 系统可视化前病毒表达动力学。
Commun Biol. 2024 Mar 20;7(1):344. doi: 10.1038/s42003-024-06025-8.
4
HIV-1 Proviral Genome Engineering with CRISPR-Cas9 for Mechanistic Studies.利用 CRISPR-Cas9 对 HIV-1 前病毒基因组进行工程改造以进行机制研究。
Viruses. 2024 Feb 13;16(2):287. doi: 10.3390/v16020287.
5
HibeRNAtion: HIV-1 RNA Metabolism and Viral Latency.HibeRNAtion:HIV-1 RNA 代谢与病毒潜伏。
Front Cell Infect Microbiol. 2022 Jun 14;12:855092. doi: 10.3389/fcimb.2022.855092. eCollection 2022.
6
Selective elimination of host cells harboring replication-competent human immunodeficiency virus reservoirs: a promising therapeutic strategy for HIV cure.选择性消除携带复制型人类免疫缺陷病毒储存库的宿主细胞:HIV 治愈的有前途的治疗策略。
Chin Med J (Engl). 2021 Oct 7;134(23):2776-2787. doi: 10.1097/CM9.0000000000001797.
7
UHRF1 Suppresses HIV-1 Transcription and Promotes HIV-1 Latency by Competing with p-TEFb for Ubiquitination-Proteasomal Degradation of Tat.UHRF1 通过与 p-TEFb 竞争泛素化-蛋白酶体降解 Tat 来抑制 HIV-1 转录并促进 HIV-1 潜伏期。
mBio. 2021 Aug 31;12(4):e0162521. doi: 10.1128/mBio.01625-21.
8
Mutations altering acetylated residues in the CTD of HIV-1 integrase cause defects in proviral transcription at early times after integration of viral DNA.HIV-1 整合酶 CTD 中乙酰化残基的突变导致病毒 DNA 整合后早期前病毒转录缺陷。
PLoS Pathog. 2020 Dec 22;16(12):e1009147. doi: 10.1371/journal.ppat.1009147. eCollection 2020 Dec.
9
A Review of Current Strategies Towards the Elimination of Latent HIV-1 and Subsequent HIV-1 Cure.消除潜伏 HIV-1 并随后实现 HIV-1 治愈的当前策略综述。
Curr HIV Res. 2021;19(1):14-26. doi: 10.2174/1570162X18999200819172009.
10
Small Molecule Targeting of Specific BAF (mSWI/SNF) Complexes for HIV Latency Reversal.小分子靶向特定 BAF(mSWI/SNF)复合物用于 HIV 潜伏逆转。
Cell Chem Biol. 2018 Dec 20;25(12):1443-1455.e14. doi: 10.1016/j.chembiol.2018.08.004. Epub 2018 Sep 6.