首页> 外文期刊>Metabolic Engineering Communications >Tet-On lentiviral transductants lose inducibility when silenced for extended intervals in mammary epithelial cells
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Tet-On lentiviral transductants lose inducibility when silenced for extended intervals in mammary epithelial cells

机译:当长时间沉默在乳腺上皮细胞中时,Tet-On慢病毒转导子失去诱导能力

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Silencing of virally transduced genes by promoter methylation and histone deacetylation has been a chronic problem both experimentally and therapeutically. We observed frequent silencing of the tetracycline-inducible Tet-On promoter borne by the Tripz lentivirus in mammary epithelial cell lines. We found that silencing could be prevented by continuous induction, but uninduced Tet-On gradually became uninducible, suggesting promoter modification. Accordingly, silencing was reversible by a common inhibitor of histone deacetylases, sodium butyrate. The effect was cell-line dependent, as HEK293 cells exhibited only moderate silencing that could be partly reversed by extended induction. These results indicate the need to test individual cell lines prior to using this system for studies that require induction after long periods of repression such as in animal models or RNA interference screens.
机译:通过启动子甲基化和组蛋白去乙酰化使病毒转导的基因沉默一直是实验和治疗上的长期问题。我们观察到Trips慢病毒携带的四环素诱导性Tet-On启动子在乳腺上皮细胞系中频繁沉默。我们发现可以通过连续诱导来防止沉默,但是未诱导的Tet-On逐渐变得不可诱导,提示启动子修饰。因此,组蛋白脱乙酰基酶的常见抑制剂丁酸钠可逆转沉默。该效应是细胞系依赖性的,因为HEK293细胞仅表现出中度沉默,而延长诱导可部分逆转该沉默。这些结果表明,在动物模型或RNA干扰筛选等经过长时间抑制后需要诱导的研究中,需要先使用单个系统进行测试。

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