Heterogeneity of chromosomal breakage levels in epithelial tissue of ataxia-telangiectasia homozygotes and heterozygotes
- PMID: 2777252
- DOI: 10.1007/BF00286705
Heterogeneity of chromosomal breakage levels in epithelial tissue of ataxia-telangiectasia homozygotes and heterozygotes
Abstract
The objective of this study was to obtain an estimate of the frequency distribution of spontaneous chromosomal breakage occurring in vivo in oral epithelia of 20 ataxia-telangiectasia patients (A-T homozygotes) and 26 parents (A-T obligate heterozygotes). Samples of exfoliated cells were obtained from each individual by swabbing the oral cavity and preparing air-dried slides. The percentage of exfoliated cells with micronuclei (MEC frequency) was used as an in vivo indicator for the amount of chromosomal breakage occurring in the tissue. As a population group, MEC frequencies of the A-T patients differed significantly from controls (mean for A-T patients, 1.51; for controls, 0.29; P less than 0.01). However, the values observed in individual patients ranged from MEC frequencies 10- to 12-fold above control values, to frequencies overlapping the upper values observed in the controls. Similarly, MEC frequencies observed among the A-T heterozygotes differed significantly from controls (mean for A-T heterozygotes, 1.02, mean for controls, 0.29; P less than 0.01). However, only 16 of the 26 individuals sampled had MEC frequencies greater than 0.5%, the 90th percentile for controls (compared with 16 of the 20 A-T patients examined). Of the A-T patients 11 had been previously assigned to complementation groups on the basis of sensitivity to x-irradiation. Seven of the patients belonged to group A and had MEC frequencies ranging from 0.3% to 1.9% with the remaining patients belonging to group C with MEC frequencies of 0.2% to 0.9%. The data presented in this paper suggest that although levels of spontaneous breakage in epithelial tissues of A-T patients and A-T obligate heterozygotes are often significantly elevated, this is not the case in all individuals.
Similar articles
-
In vivo chromosomal instability in ataxia-telangiectasia homozygotes and heterozygotes.Hum Genet. 1986 Dec;74(4):335-40. doi: 10.1007/BF00280482. Hum Genet. 1986. PMID: 3793095
-
Radiation-induced G2 delay and spontaneous chromosome aberrations in ataxia-telangiectasia homozygotes and heterozygotes.Int J Radiat Biol. 1994 Dec;66(6 Suppl):S157-63. Int J Radiat Biol. 1994. PMID: 7836843
-
Chromosomal instability in ataxia telangiectasia.Cancer Genet Cytogenet. 1982 Aug;6(4):289-302. doi: 10.1016/0165-4608(82)90085-1. Cancer Genet Cytogenet. 1982. PMID: 7116322
-
Possible role of chromatin alteration in the radiosensitivity of ataxia-telangiectasia.Int J Radiat Biol. 1994 Dec;66(6 Suppl):S109-13. Int J Radiat Biol. 1994. PMID: 7836837 Review.
-
[Ataxia telangiectasia: what impact in clinical oncology?].Bull Cancer. 1992;79(7):645-50. Bull Cancer. 1992. PMID: 1467590 Review. French.
Cited by
-
Factors Affecting the Nuclei in Newborn and Children.Int J Environ Res Public Health. 2022 Apr 1;19(7):4226. doi: 10.3390/ijerph19074226. Int J Environ Res Public Health. 2022. PMID: 35409906 Free PMC article. Review.
-
Heterogeneity in the clastogenic response to X-rays in lymphocytes from ataxia-telangiectasia heterozygotes and controls.Cancer Causes Control. 1992 May;3(3):237-45. doi: 10.1007/BF00124257. Cancer Causes Control. 1992. PMID: 1610970
-
Micronuclei in neonates and children: effects of environmental, genetic, demographic and disease variables.Mutagenesis. 2011 Jan;26(1):51-6. doi: 10.1093/mutage/geq064. Mutagenesis. 2011. PMID: 21164182 Free PMC article. Review.
References
Publication types
MeSH terms
LinkOut - more resources
Other Literature Sources
Medical
Research Materials