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海胆sns5绝缘子通过维持活跃的染色质结构来保护逆转录病毒载体免受染色体位置效应的影响。

The sea urchin sns5 insulator protects retroviral vectors from chromosomal position effects by maintaining active chromatin structure.

作者信息

D'Apolito Danilo, Baiamonte Elena, Bagliesi Mariella, Di Marzo Rosalba, Calzolari Roberta, Ferro Leda, Franco Vito, Spinelli Giovanni, Maggio Aurelio, Acuto Santina

机构信息

Unità di Ricerca P. Cutino, U.O.C. Ematologia II, A.O. V. Cervello, Palermo, Italy.

出版信息

Mol Ther. 2009 Aug;17(8):1434-41. doi: 10.1038/mt.2009.74. Epub 2009 Apr 7.

Abstract

Silencing and position-effect (PE) variegation (PEV), which is due to integration of viral vectors in heterochromatin regions, are considered significant obstacles to obtaining a consistent level of transgene expression in gene therapy. The inclusion of chromatin insulators into vectors has been proposed to counteract this position-dependent variegation of transgene expression. Here, we show that the sea urchin chromatin insulator, sns5, protects a recombinant gamma-retroviral vector from the negative influence of chromatin in erythroid milieu. This element increases the probability of vector expression at different chromosomal integration sites, which reduces both silencing and PEV. By chromatin immunoprecipitation (ChIP) analysis, we demonstrated the specific binding of GATA1 and OCT1 transcription factors and the enrichment of hyperacetylated nucleosomes to sns5 sequences. The results suggest that this new insulator is able to maintain a euchromatin state inside the provirus locus with mechanisms that are common to other characterized insulators. On the basis of its ability to function as barrier element in erythroid milieu and to bind the erythroid specific factor GATA1, the inclusion of sns5 insulator in viral vectors may be of practical benefit in gene transfer applications and, in particular, for gene therapy of erythroid disorders.

摘要

沉默和位置效应(PE)斑驳(PEV)是由于病毒载体整合到异染色质区域所致,被认为是在基因治疗中获得一致水平转基因表达的重大障碍。有人提出在载体中加入染色质绝缘子来对抗转基因表达的这种位置依赖性斑驳。在这里,我们表明海胆染色质绝缘子sns5可保护重组γ-逆转录病毒载体免受红系环境中染色质的负面影响。该元件增加了载体在不同染色体整合位点表达的概率,从而减少了沉默和PEV。通过染色质免疫沉淀(ChIP)分析,我们证明了GATA1和OCT1转录因子与sns5序列的特异性结合以及超乙酰化核小体的富集。结果表明,这种新的绝缘子能够通过与其他已鉴定绝缘子共有的机制在原病毒基因座内维持常染色质状态。基于其在红系环境中作为屏障元件的功能以及与红系特异性因子GATA1结合的能力,在病毒载体中加入sns5绝缘子可能在基因转移应用中具有实际益处,特别是对于红系疾病的基因治疗。

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