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本文引用的文献

1
HP1: heterochromatin binding proteins working the genome.HP1:异染色质结合蛋白作用于基因组。
Epigenetics. 2010 May 16;5(4):287-92. doi: 10.4161/epi.5.4.11683. Epub 2010 May 3.
2
Antiretroviral intensification and valproic acid lack sustained effect on residual HIV-1 viremia or resting CD4+ cell infection.抗逆转录病毒强化治疗和丙戊酸缺乏对残留 HIV-1 病毒血症或静止 CD4+ 细胞感染的持续作用。
PLoS One. 2010 Feb 23;5(2):e9390. doi: 10.1371/journal.pone.0009390.
3
No evidence for decay of the latent reservoir in HIV-1-infected patients receiving intensive enfuvirtide-containing antiretroviral therapy.在接受强化含恩夫韦肽的抗逆转录病毒治疗的 HIV-1 感染患者中,没有潜伏储库衰减的证据。
J Infect Dis. 2010 Jan 15;201(2):293-6. doi: 10.1086/649569.
4
Molecular control of HIV-1 postintegration latency: implications for the development of new therapeutic strategies.HIV-1 整合后潜伏的分子调控:对新治疗策略发展的启示。
Retrovirology. 2009 Dec 4;6:111. doi: 10.1186/1742-4690-6-111.
5
Evidence for a lack of a direct transcriptional suppression of the iron regulatory peptide hepcidin by hypoxia-inducible factors.没有证据表明缺氧诱导因子直接转录抑制铁调节肽 hepcidin。
PLoS One. 2009 Nov 18;4(11):e7875. doi: 10.1371/journal.pone.0007875.
6
HIV-1 regulation of latency in the monocyte-macrophage lineage and in CD4+ T lymphocytes.HIV-1 对单核细胞-巨噬细胞谱系和 CD4+ T 淋巴细胞中的潜伏期的调控。
J Leukoc Biol. 2010 Apr;87(4):575-88. doi: 10.1189/jlb.0409264. Epub 2009 Oct 2.
7
Short communication: activation of latent HIV type 1 gene expression by suberoylanilide hydroxamic acid (SAHA), an HDAC inhibitor approved for use to treat cutaneous T cell lymphoma.简短通讯:用于治疗皮肤T细胞淋巴瘤的获批药物——辛二酰苯胺异羟肟酸(SAHA)激活潜伏的1型人类免疫缺陷病毒基因表达
AIDS Res Hum Retroviruses. 2009 Sep;25(9):883-7. doi: 10.1089/aid.2008.0294.
8
Resveratrol inhibited Tat-induced HIV-1 LTR transactivation via NAD(+)-dependent SIRT1 activity.白藜芦醇通过依赖烟酰胺腺嘌呤二核苷酸(NAD(+))的沉默信息调节因子1(SIRT1)活性抑制反式激活因子(Tat)诱导的HIV-1长末端重复序列(LTR)反式激活。
Life Sci. 2009 Sep 23;85(13-14):484-9. doi: 10.1016/j.lfs.2009.07.014. Epub 2009 Aug 5.
9
Expression of latent human immunodeficiency type 1 is induced by novel and selective histone deacetylase inhibitors.新型且选择性的组蛋白去乙酰化酶抑制剂可诱导潜伏型人类免疫缺陷病毒 1 的表达。
AIDS. 2009 Sep 10;23(14):1799-806. doi: 10.1097/QAD.0b013e32832ec1dc.
10
p21(WAF1) gene promoter is epigenetically silenced by CTIP2 and SUV39H1.p21(WAF1)基因启动子被CTIP2和SUV39H1表观遗传沉默。
Oncogene. 2009 Sep 24;28(38):3380-9. doi: 10.1038/onc.2009.193. Epub 2009 Jul 6.

病毒感染中的组蛋白去乙酰化酶。

Histone deacetylases in viral infections.

出版信息

Clin Epigenetics. 2010 Sep;1(1-2):13-24. doi: 10.1007/s13148-010-0003-5. Epub 2010 May 30.

DOI:10.1007/s13148-010-0003-5
PMID:22704086
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3365363/
Abstract

Chromatin remodeling and gene expression are regulated by histone deacetylases (HDACs) that condense the chromatin structure by deacetylating histones. HDACs comprise a group of enzymes that are responsible for the regulation of both cellular and viral genes at the transcriptional level. In mammals, a total of 18 HDACs have been identified and grouped into four classes, i.e., class I (HDACs 1, 2, 3, 8), class II (HDACs 4, 5, 6, 7, 9, 10), class III (Sirt1-Sirt7), and class IV (HDAC11). We review here the role of HDACs on viral replication and how HDAC inhibitors could potentially be used as new therapeutic tools in several viral infections.

摘要

组蛋白去乙酰化酶(HDACs)通过去乙酰化组蛋白来调节染色质结构,从而调节染色质重塑和基因表达。HDACs 是一组酶,负责在转录水平上调节细胞和病毒基因。在哺乳动物中,已经鉴定出总共 18 种 HDACs,并分为四类,即 I 类(HDACs 1、2、3、8)、II 类(HDACs 4、5、6、7、9、10)、III 类(Sirt1-Sirt7)和 IV 类(HDAC11)。在这里,我们综述了 HDACs 在病毒复制中的作用,以及 HDAC 抑制剂如何可能成为几种病毒感染的新治疗工具。