Literature DB >> 36066712

Cytokinesis Blocked Micronuclei Aberration Analysis.

Takamitsu A Kato1.   

Abstract

Cytokinesis blocked micronuclei (CBMN) assay is a rapid and sensitive analysis of chromosome aberrations and miss assortments during cell division. Genotoxic agent exposure produces DNA damage and chromosome fragments. Fragmented chromosomes without centromere failed to attach kinetochore which segregates a pair of homologous chromosomes to each daughter cells at cytokinesis, hence leading to form micronuclei. Chromosome or fragments of chromosome can also form micronuclei when they are not accurately sorted to daughter cells. Using cytochalasin B, an actin inhibitor, blocks cytokinesis of which completion leads serration appearance formed with two daughter cells while nuclei segregation is undergoing. As a result, one cell having two daughter nuclei, i.e., binucleated cell, is produced. By analyzing these binucleated cells, chromosome aberrations can be estimated as well as popular chromosome aberration analysis. Frequency of micronuclei formation predicts the testing agents' genotoxicity. By combining use with centromere-specific probes or DNA damage signal probes, the nature of genotoxicity of tested agents can be estimated.
© 2023. The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature.

Entities:  

Keywords:  Cytochalasin B; Cytokinesis blocked micronucleus (CBMN) assay; Genotoxicity; Nuclear segregation

Mesh:

Substances:

Year:  2023        PMID: 36066712     DOI: 10.1007/978-1-0716-2433-3_9

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  9 in total

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Journal:  Mutat Res       Date:  1986-07       Impact factor: 2.433

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Journal:  Mutat Res       Date:  1973-05       Impact factor: 2.433

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Journal:  Mutat Res       Date:  1976-12       Impact factor: 2.433

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Journal:  Mutat Res       Date:  1983-06       Impact factor: 2.433

9.  Kinetochore structure, duplication, and distribution in mammalian cells: analysis by human autoantibodies from scleroderma patients.

Authors:  S Brenner; D Pepper; M W Berns; E Tan; B R Brinkley
Journal:  J Cell Biol       Date:  1981-10       Impact factor: 10.539

  9 in total

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