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Recent developments in the assessment of chromosomal damage.

Abstract
Ionizing radiation and restriction endonucleases are very efficient in inducing chromosomal aberrations (CAs). These aberrations are mainly consequences of misrepair of DNA double-strand breaks (DSBs). The fast repairing component of DSBs induced by ionizing radiation seems to be responsible for exchange aberration. Use of premature chromosome condensation technique in combination with DNA repair inhibitors such as ara A has given valuable information on the assessment of the frequencies of initial chromosome breaks and the kinetics of their repair following low LET radiation. The recently developed 'chromosome painting' technique using chromosome-specific libraries has also increased considerably the resolution of identifying and scoring of CAs. After low LET radiation, stable chromosome exchanges (translocations) are induced more frequently than unstable chromosome exchanges (dicentrics). Fluorescence in situ hybridization employing telomeric probe has made it possible to score efficiently exchange aberrations involving the acrocentric chromosomes of mouse. Chinese hamster cells have several intercalary telomeric sequences present in most of the chromosomes. These telomeric blocks have been found to be associated with chromosomal aberrations induced by restriction endonucleases and short wave UV and evidence has been obtained for apparent amplification of telomeric sequences at the break points.
AuthorsA T Natarajan, A S Balajee, J J Boei, S Chatterjee, F Darroudi, M Grigorova, M Noditi, H J Oh, P Slijepcevic, S Vermeulen
JournalInternational journal of radiation biology (Int J Radiat Biol) Vol. 66 Issue 5 Pg. 615-23 (Nov 1994) ISSN: 0955-3002 [Print] England
PMID7983455 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Topics
  • Aneuploidy
  • Animals
  • CHO Cells
  • Cells, Cultured
  • Chromosome Aberrations
  • Cricetinae
  • DNA Damage
  • DNA Repair
  • Humans
  • Mice
  • Repetitive Sequences, Nucleic Acid
  • Translocation, Genetic

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