The most common fragile site in man is 3p14
- 1 March 1986
- journal article
- research article
- Published by Springer Nature in Human Genetics
- Vol. 72 (3) , 215-220
- https://doi.org/10.1007/bf00291880
Abstract
In man a common fragile site is known to occur at 3p14. We studied the expression of this fragility in a group of 70 normal healthy subjects. Chromosome breaks, chromatid breaks and gaps at 3p14 could be observed in every examined individual, and in a total of 7000 metaphases they were seen in a mean of 4% of cells. Fluorescence studies in ten persons with chromosome No. 3 polymorphism showed that in all cases both Nos. 3 were about equally liable to breakage. A considerable variation in the fra 3p14 expression was found between individuals as well as in repeated cultures from the same person. Neither sex nor age influences could be detected. Cultures with a high percentage of lesions at 3p14 tended to have also a high number of lesions at other sites. Methotrexate and fluorodeoxyuridine markedly enhanced the expression of fra 3p14 and other fragilities. It is concluded that the chromosomal region at 3p14 represents man's most common fragile site, the expression of which seems to be influenced by environmental and heritable factors.This publication has 31 references indexed in Scilit:
- Cytogenetics of the human benign mixed salivary gland tumourHereditas, 2008
- Excess thymidine induces folate sensitve fragile sitesAmerican Journal of Medical Genetics, 1985
- Absence of significant autosomal lesions in Huntington's diseaseAnnals of Human Genetics, 1985
- Nonrandom chromosome alterations in rhabdomyosarcomaCancer Genetics and Cytogenetics, 1985
- Cancer chromosome breakpoints and common fragile sites induced by aphidicolinCancer Genetics and Cytogenetics, 1984
- Constitutive fragile sites 1p31, 3p14, 6q26, and 16q23 and their use as controls for false‐negative results with the fragile(X)American Journal of Medical Genetics, 1984
- Fragile sites and cancer breakpointsCancer Genetics and Cytogenetics, 1984
- Involvement of band 3p14 in t(3;8) hereditary renal carcinomaCancer Genetics and Cytogenetics, 1984
- Chromosomal breakage in normal and fragile X subjects using low folate culture conditions.Journal of Medical Genetics, 1983
- Hereditary Renal-Cell Carcinoma Associated with a Chromosomal TranslocationNew England Journal of Medicine, 1979