The use of the in vitro micronucleus assay to detect and assess the aneugenic activity of chemicals

被引:17
作者
Parry, James M. [1 ]
Parry, Elizabeth M. [1 ]
机构
[1] Univ Coll Swansea, Sch Biol Sci, Ctr Mol Genet & Toxicol, Swansea SA2 8PP, W Glam, Wales
关键词
D O I
10.1016/j.mrgentox.2006.04.007
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The successful validation of the in vitro micronucleus assay by the SFTG now provides the opportunity for this highly cost effective assay to be used to screen chemicals for their ability to induce both structural (clastogenic) and numerical (aneugenic) chromosome changes using interphase cells. The use of interphase cells and a relatively simple experimental protocol provides the opportunity to greatly increase the statistical power of cytogenetic studies on chemical interactions. The application of molecular probes capable of detecting kinetochores and centromeres provides the opportunity to classify mechanisms of micronuclcus induction into those which are primarily due to chromosome loss or breakage. When a predominant mechanism of micronucleus induction has been shown to be based upon chromosome loss then further investigation can involve the determination of the role of non-disjunction in the induction of aneuploidy. The binucleate cell modification of the in vitro micronucleus assay can be combined with the use of chromosome specific centromere probes to determine the segregation of individual chromosomes into daughter nuclei. The combination of these methods provides us with powerful tools for the investigation of mechanisms of genotoxicity particularly in the low dose regions. (c) 2006 Elsevier B.V. All rights reserved.
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页码:5 / 8
页数:4
相关论文
共 27 条
[1]   USE OF A CENTROMERE-SPECIFIC DNA PROBE (P82H) IN NONISOTOPIC INSITU HYBRIDIZATION FOR CLASSIFICATION OF MICRONUCLEI [J].
BECKER, P ;
SCHERTHAN, H ;
ZANKL, H .
GENES CHROMOSOMES & CANCER, 1990, 2 (01) :59-62
[2]   Evaluation of thresholds for benomyl- and carbendazim-induced aneuploidy in cultured human lymphocytes using fluorescence in situ hybridization [J].
Bentley, KS ;
Kirkland, D ;
Murphy, M ;
Marshall, R .
MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS, 2000, 464 (01) :41-51
[3]   THE ANALYSIS OF 10 POTENTIAL SPINDLE POISONS FOR THEIR ABILITY TO INDUCE CREST-POSITIVE MICRONUCLEI IN HUMAN-DIPLOID FIBROBLASTS [J].
BONATTI, S ;
CAVALIERI, Z ;
VIAGGI, S ;
ABBONDANDOLO, A .
MUTAGENESIS, 1992, 7 (02) :111-114
[4]   A combination of the micronucleus assay and a FISH technique for evaluation of the genotoxicity of 1,2,4-benzenetriol [J].
Chung, HW ;
Kang, SJ ;
Kim, SY .
MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS, 2002, 516 (1-2) :49-56
[5]   MEASUREMENT OF LEVELS OF ANEUPLOIDY IN MAMMALIAN-CELLS USING A MODIFIED HYPOTONIC TREATMENT [J].
DANFORD, N .
MUTATION RESEARCH, 1984, 139 (03) :127-132
[6]   IMMUNOFLUORESCENT STAINING OF KINETOCHORES IN MICRONUCLEI - A NEW ASSAY FOR THE DETECTION OF ANEUPLOIDY [J].
DEGRASSI, F ;
TANZARELLA, C .
MUTATION RESEARCH, 1988, 203 (05) :339-345
[7]  
*DEP HLTH, 2000, COM GUID STRAT TEST
[8]   A study of the aneugenic activity of trichlorfon detected by centromere-specific probes in human lymphoblastoid cell lines [J].
Doherty, AT ;
Ellard, S ;
Parry, EM ;
Parry, JM .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 1996, 372 (02) :221-231
[9]   KINETOCHORE LOCALIZATION IN MICRONUCLEATED CYTOKINESIS-BLOCKED CHINESE-HAMSTER OVARY CELLS - A NEW AND RAPID ASSAY FOR IDENTIFYING ANEUPLOIDY-INDUCING AGENTS [J].
EASTMOND, DA ;
TUCKER, JD .
MUTATION RESEARCH, 1989, 224 (04) :517-525
[10]   DETECTION OF HYPERDIPLOIDY AND CHROMOSOME BREAKAGE IN INTERPHASE HUMAN-LYMPHOCYTES FOLLOWING EXPOSURE TO THE BENZENE METABOLITE HYDROQUINONE USING MULTICOLOR FLUORESCENCE IN-SITU HYBRIDIZATION WITH DNA PROBES [J].
EASTMOND, DA ;
RUPA, DS ;
HASEGAWA, LS .
MUTATION RESEARCH, 1994, 322 (01) :9-20