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DNA转染后拓扑异构酶IIα的抑制作用极大地增强了人前B淋巴细胞系中的随机整合。

Topoisomerase IIalpha inhibition following DNA transfection greatly enhances random integration in a human pre-B lymphocyte cell line.

作者信息

Toyoda Eriko, Kurosawa Aya, Kamekawa Haruna, Adachi Noritaka

机构信息

International Graduate School of Arts and Sciences, Yokohama City University, 22-2 Seto, Kanazawa-ku, Yokohama 236-0027, Japan.

出版信息

Biochem Biophys Res Commun. 2009 May 8;382(3):492-6. doi: 10.1016/j.bbrc.2009.03.047. Epub 2009 Mar 13.

Abstract

DNA transfection can be too inefficient to establish a desired number of stable transfectants, particularly in lymphocytes; however, this could be circumvented by increasing the absolute frequency of random integration. In this paper, we show that treating cells with topoisomerase II inhibitor following electroporation greatly (approximately 10- to 20-fold) enhances random integration of input DNA in a human pre-B lymphocyte cell line, Nalm-6. With the use of various kinds of topoisomerase II-targeting agents, we also present evidence that topoisomerase IIalpha inhibition is critical for the enhancement of random integration, while the contribution of topoisomerase IIbeta may be negligible. As topoisomerase IIalpha is highly expressed in vigorously growing cells, our results show that topoisomerase IIalpha inhibition provides a promising way of enhancing random integration in virtually all cultured cell lines.

摘要

DNA转染效率可能过低,难以获得所需数量的稳定转染子,在淋巴细胞中尤其如此;然而,这一问题可通过提高随机整合的绝对频率来解决。在本文中,我们表明,在电穿孔后用拓扑异构酶II抑制剂处理细胞,可极大地(约10至20倍)增强人前B淋巴细胞系Nalm-6中输入DNA的随机整合。通过使用各种靶向拓扑异构酶II的试剂,我们还提供了证据表明,抑制拓扑异构酶IIα对增强随机整合至关重要,而拓扑异构酶IIβ的作用可能微不足道。由于拓扑异构酶IIα在快速生长的细胞中高度表达,我们的结果表明,抑制拓扑异构酶IIα为增强几乎所有培养细胞系中的随机整合提供了一种有前景的方法。

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