DETECTION OF RECOMBINATIONAL MUTATIONS IN CULTURED HUMAN-CELLS BY SOUTHERN BLOT ANALYSIS WITH MINISATELLITE DNA PROBES
被引:12
作者:
HONMA, M
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机构:Division of Genetics and Mutagenesis, National Institute of Hygienic Sciences, Tokyo
HONMA, M
KATAOKA, E
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机构:Division of Genetics and Mutagenesis, National Institute of Hygienic Sciences, Tokyo
KATAOKA, E
OHNISHI, K
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机构:Division of Genetics and Mutagenesis, National Institute of Hygienic Sciences, Tokyo
OHNISHI, K
KIKUNO, T
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机构:Division of Genetics and Mutagenesis, National Institute of Hygienic Sciences, Tokyo
KIKUNO, T
HAYASHI, M
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机构:Division of Genetics and Mutagenesis, National Institute of Hygienic Sciences, Tokyo
HAYASHI, M
SOFUNI, T
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机构:Division of Genetics and Mutagenesis, National Institute of Hygienic Sciences, Tokyo
SOFUNI, T
MIZUSAWA, H
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机构:Division of Genetics and Mutagenesis, National Institute of Hygienic Sciences, Tokyo
MIZUSAWA, H
机构:
[1] Division of Genetics and Mutagenesis, National Institute of Hygienic Sciences, Tokyo
来源:
MUTATION RESEARCH
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1993年
/
286卷
/
02期
关键词:
RECOMBINATIONAL MUTATION;
MINISATELLITE DNA;
DNA FINGERPRINT;
MUTAGENICITY TESTING;
D O I:
10.1016/0027-5107(93)90180-N
中图分类号:
Q3 [遗传学];
学科分类号:
071007 ;
090102 ;
摘要:
Using the human acute monocytic leukemia cell line, THP-1, a hypermutability of minisatellite loci was demonstrated in cell culture by Southern blot analysis with minisatellite DNA probes. DNA was isolated from 98 subclones and hybridized to a panel of minisatellite probes consisting of three multilocus minisatellite probes (ML probes) and seven locus-specific minisatellite probes (LS probes). The Southern blot patterns of the hybridized subclones were compared with those of the parental THP-1. Four mutated bands with two ML probes and two mutated bands with two LS probes were detected. The mutation frequency was estimated roughly at 0.1% based on the total number of bands analyzed, and it was much higher than that expected for other DNA regions. Four of these mutations were thought to be alterations of repetitions caused by insertion or deletion of tandem repeats, and one mutant lost a complete minisatellite allele. The nature of the sixth mutant was unclear. Because of the hypermutability of minisatellite DNA, Southern blot analysis using minisatellite DNA probes can be used as a mutation assay system directly based on the DNA.