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带有条件着丝粒的人源人工染色体,用于基因递送和基因表达。

Human artificial chromosome with a conditional centromere for gene delivery and gene expression.

机构信息

Department of Biomedical Science, Institute of Regenerative Medicine and Biofunction, Graduate School of Medical Sciences, Tottori University, Nishi-cho, Yonago, Tottori, Japan.

出版信息

DNA Res. 2010 Oct;17(5):293-301. doi: 10.1093/dnares/dsq020. Epub 2010 Aug 26.

Abstract

Human artificial chromosomes (HACs), which carry a fully functional centromere and are maintained as a single-copy episome, are not associated with random mutagenesis and offer greater control over expression of ectopic genes on the HAC. Recently, we generated a HAC with a conditional centromere, which includes the tetracycline operator (tet-O) sequence embedded in the alphoid DNA array. This conditional centromere can be inactivated, loss of the alphoid(tet-O) (tet-O HAC) by expression of tet-repressor fusion proteins. In this report, we describe adaptation of the tet-O HAC vector for gene delivery and gene expression in human cells. A loxP cassette was inserted into the tet-O HAC by homologous recombination in chicken DT40 cells following a microcell-mediated chromosome transfer (MMCT). The tet-O HAC with the loxP cassette was then transferred into Chinese hamster ovary cells, and EGFP transgene was efficiently and accurately incorporated into the tet-O HAC vector. The EGFP transgene was stably expressed in human cells after transfer via MMCT. Because the transgenes inserted on the tet-O HAC can be eliminated from cells by HAC loss due to centromere inactivation, this HAC vector system provides important novel features and has potential applications for gene expression studies and gene therapy.

摘要

人类人工染色体(HACs)携带一个功能完整的着丝粒,并作为单拷贝的附加体维持,它们不会与随机突变有关,并能更好地控制 HAC 上异位基因的表达。最近,我们构建了一个带有条件着丝粒的 HAC,其中包含四环素操纵子(tet-O)序列嵌入着丝粒 DNA 阵列中。这个条件着丝粒可以通过表达 tet 抑制剂融合蛋白失活,导致着丝粒(tet-O)丢失(tet-O HAC)。在本报告中,我们描述了 tet-O HAC 载体在人类细胞中的基因传递和表达的适应性。在鸡 DT40 细胞中通过同源重组插入 loxP 盒,随后通过微细胞介导的染色体转移(MMCT)将其转移到 tet-O HAC 中。然后将带有 loxP 盒的 tet-O HAC 转移到中国仓鼠卵巢细胞中,EGFP 转基因可以有效地、准确地整合到 tet-O HAC 载体中。通过 MMCT 转移后,EGFP 转基因在人类细胞中稳定表达。因为由于着丝粒失活导致 HAC 丢失,插入到 tet-O HAC 上的转基因可以从细胞中消除,所以这个 HAC 载体系统提供了重要的新特性,并具有用于基因表达研究和基因治疗的潜在应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c97/2955713/811443a535d1/dsq02001.jpg

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