Abstract
Chromosome aberration analysis has been the basis of one of core tests in genetic toxicology since guidelines were first established (DHSS (1981) Guidelines for the Testing of Chemicals for Mutagenicity. Prepared by the Committee on Mutagenicity of Chemcials in Food, Consumer Products, and the Environment, Department of Health and Social Security. Report on Health and Social Subjects, No. 24. Her Majesty’s Stationery Office, London; IPCS (1985) Guide to short-term tests for detecting mutagenic and carcinogenic chemicals prepared for the IPCS by the International Commission for Protection against Environmental Mutagens and Carcinogens. Geneva, WHO). The technique consists of microscope examination of preparations of chromosomes, usually mammalian, for clastogenicity (chromosome breakage events), and agents which induce such changes are considered genotoxic.
There are a number of different types of aberrations, and within types, considerable variation in their appearance. This chapter addresses aberration classification, their appearance, frequency and fate, and the range within aberration types, potential mis-classifications, and data recording and interpretation.
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References
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Acknowledgements
The author is very grateful for discussions on practicalities of scoring chromosome aberrations from cytogeneticists in a number of laboratories, in particularly the following: CiToxLAB France, Covance Laboratories Ltd., Harrogate, UK, Sanofi-Aventis Alfortville, France and Frankfurt, Deutchland, and Sequani Ltd., Ledbury, UK.
Thanks also to Paul Fowler (Covance) for information on variation in cell selection between analysts.
For information on training courses in chromosome aberration analysis, go to http://www.microptic.com.
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Danford, N. (2012). The Interpretation and Analysis of Cytogenetic Data. In: Parry, J., Parry, E. (eds) Genetic Toxicology. Methods in Molecular Biology, vol 817. Springer, New York, NY. https://doi.org/10.1007/978-1-61779-421-6_6
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DOI: https://doi.org/10.1007/978-1-61779-421-6_6
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