The human pre-B cell line Nalm-6 is highly proficient in gene targeting by homologous recombination

被引:52
作者
Adachi, N
So, S
Iiizumi, S
Nomura, Y
Murai, K
Yamakawa, C
Miyagawa, K
Koyama, H
机构
[1] Yokohama City Univ, Kihara Inst Biol Res, Grad Sch Integrated Sci, Yokohama, Kanagawa 2440813, Japan
[2] Univ Tokyo, Grad Sch Med, Dept Radiat Oncol, Tokyo, Japan
关键词
D O I
10.1089/dna.2006.25.19
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Gene targeting provides a powerful means for analyzing gene function, as exemplified by knockout mouse studies and recent work with the highly recombinogenic chicken DT40 B-lymphocyte line. In human cultured cells, however, the low frequency of gene targeting is a serious barrier to efficiently generate knockout clones. Moreover, commonly used human cell lines are karyotypically abnormal or unstable. Here, we show using promoterless targeting constructs that Nalm-6, a human pre-B ALL cell line, is highly proficient for gene targeting by homologous recombination. Indeed, the efficiency of TP53 gene targeting in Nalm-6 appears nearly two orders of magnitude higher than that in HCT116, a colon cancer cell line popularly used for gene targeting. Expression analysis revealed a lack of MSH2 expression in this cell line. As Nalm-6 has a stable neardiploid karyotype with normal p53 status, our results underscore the usefulness of Nalm-6 for gene knockout studies in humans.
引用
收藏
页码:19 / 24
页数:6
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