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通过减轻 Rous 肉瘤病毒启动子的 CpG 甲基化来重新激活转基因鹌鹑细胞中的转基因表达。

Reactivation of transgene expression by alleviating CpG methylation of the Rous sarcoma virus promoter in transgenic quail cells.

机构信息

Department of Agricultural Biotechnology, Seoul National University, 599 Gwanak-ro, Gwanak-gu Seoul 151-921, Korea.

出版信息

Mol Biotechnol. 2011 Nov;49(3):222-8. doi: 10.1007/s12033-011-9393-7.

Abstract

In this study, we investigated the relative expression of the Rous sarcoma virus (RSV) promoter-driven expression of enhanced green fluorescent protein (EGFP) in fibroblasts of transgenic quails. We analyzed the direct influence of CpG methylation of the RSV promoter on the transcriptional activity of delivered transgenes. Embryonic fibroblasts collected from homozygous transgenic quail (TQ2) were treated with 50 μM of DNA methyltransferase inhibitor followed by 5-aza-2'-deoxycytidine (5-azadC) for 48 h, and changes in expression were then analyzed by flow cytometry. The results show a significant increase of EGFP expression in TQ2 embryonic fibroblasts (QEFs) (2.64% to 79.84%). Subsequent methylation-specific amplification revealed that 5-azadC significantly reduced the CpG methylation status in the RSV promoters of the QEFs (86.42 to 48.41%); even after 5-azadC was withdrawn, CpG methylation remained decreased in expanded culture (16.28%). Further analysis showed that potential transcription factor binding sites existed in the CpG methylation site of the RSV promoter. These results may provide the basis for understanding the epigenetic mechanism responsible for transgenic animal production and genetic preservation.

摘要

在这项研究中,我们研究了 Rous 肉瘤病毒(RSV)启动子驱动增强型绿色荧光蛋白(EGFP)在转基因鹌鹑成纤维细胞中的相对表达。我们分析了 RSV 启动子的 CpG 甲基化对转导基因转录活性的直接影响。从纯合转基因鹌鹑(TQ2)中收集胚胎成纤维细胞,用 50μM 的 DNA 甲基转移酶抑制剂处理,然后用 5-氮杂-2'-脱氧胞苷(5-azadC)处理 48 小时,然后通过流式细胞术分析表达变化。结果表明,TQ2 胚胎成纤维细胞(QEFs)中的 EGFP 表达显著增加(2.64%至 79.84%)。随后的甲基化特异性扩增表明,5-azadC 显著降低了 QEFs 中 RSV 启动子的 CpG 甲基化状态(86.42 至 48.41%);即使在 5-azadC 撤出后,扩展培养中的 CpG 甲基化仍保持降低(16.28%)。进一步分析表明,RSV 启动子的 CpG 甲基化位点存在潜在的转录因子结合位点。这些结果可能为理解负责转基因动物生产和遗传保存的表观遗传机制提供依据。

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