Silencing of transgene expression in mammalian cells by DNA methylation and histone modifications in gene therapy perspective

被引:25
|
作者
Alhaji, Suleiman Yusuf [1 ,2 ]
Ngai, Siew Ching [3 ]
Abdullah, Syahril [1 ,4 ]
机构
[1] Univ Putra Malaysia, Fac Med & Hlth Sci, Dept Biomed Sci, Med Genet Lab, Serdang, Malaysia
[2] Abubakar Tafawa Balewa Univ Bauchi, Coll Med Sci, Dept Human Anat, Bauchi, Nigeria
[3] Univ Nottingham Malaysia, Sch Biosci, Fac Sci, Semenyih, Malaysia
[4] Univ Putra Malaysia, Inst Biosci, UPM MAKNA Canc Res Lab, Serdang, Malaysia
来源
BIOTECHNOLOGY AND GENETIC ENGINEERING REVIEWS, VOL 35 | 2019年 / 35卷
关键词
DNA methylation; histone modification; transgene repression; gene therapy; EMBRYONIC STEM-CELLS; CHRONIC GRANULOMATOUS-DISEASE; SLEEPING-BEAUTY TRANSPOSITION; PERIPHERAL-BLOOD PROGENITORS; CPG-FREE PLASMIDS; EPIGENETIC MODULATION; EXTENSIVE METHYLATION; CHROMATIN-REMODELERS; LENTIVIRAL VECTORS; DIVERSE FUNCTIONS;
D O I
10.1080/02648725.2018.1551594
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
DNA methylation and histone modifications are vital in maintaining genomic stability and modulating cellular functions in mammalian cells. These two epigenetic modifications are the most common gene regulatory systems known to spatially control gene expression. Transgene silencing by these two mechanisms is a major challenge to achieving effective gene therapy for many genetic conditions. The implications of transgene silencing caused by epigenetic modifications have been extensively studied and reported in numerous gene delivery studies. This review highlights instances of transgene silencing by DNA methylation and histone modification with specific focus on the role of these two epigenetic effects on the repression of transgene expression in mammalian cells from integrative and non-integrative based gene delivery systems in the context of gene therapy. It also discusses the prospects of achieving an effective and sustained transgene expression for future gene therapy applications.
引用
收藏
页码:1 / 25
页数:25
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