The fragile site (16) (q22)
- 1 September 1986
- journal article
- research article
- Published by Springer Nature in Human Genetics
- Vol. 74 (1) , 67-73
- https://doi.org/10.1007/bf00278788
Abstract
The rare fragile site at 16q22 was experimentally induced in lymphocyte cultures with various AT-specific, non-intercalating DNA-ligands. The optimum conditions for the induction of fra (16)(q22) were determined. The best expression of fra (16)(q22) was found with the aromatic diamidine berenil which is recommended for further studies on this fragile site. The results indicate that fra (16)(q22) is a region with AT-rich, late replicating DNA. The simultaneous treatment of lymphocytes with berenil and aphidicolin (inhibitor of DNA polymerase α) induces both the rare fra (16) (q22) and the common fra (16) (q23) within the same chromosome. A population study on 350 unselected individuals showed that fra (16)(q22) is the most common of all rare autosomal fragile sites in man. The frequency of individuals heterozygous for fra (16)(q22) is 5.1% no homozygosity for fra (16) (q22) was detected. Statistical analysis indicates that the population is in Hardy-Weinberg equilibrium with respect to the fragile and non-fragile chromosomes 16.Keywords
This publication has 36 references indexed in Scilit:
- Heritable fragile sites on human chromosomes XII. Population CytogeneticsAnnals of Human Genetics, 1985
- Report of the committee on chromosome rearrangements in neoplasia and on fragile sitesCytogenetic and Genome Research, 1985
- Fragile sites and cancer breakpointsCancer Genetics and Cytogenetics, 1984
- Cancer biology: Heritable fragile sites in cancerNature, 1984
- The marker (X) syndrome: a cytogenetic and genetic analysisAnnals of Human Genetics, 1984
- Enhancement of a fra(16)(q22) with distamycin A: A family ascertained through an abnormal propositaAmerican Journal of Medical Genetics, 1983
- EPSTEIN-BARR VIRUS AND CHROMOSOMAL DEFECTS: A FAMILY STUDYThe Lancet, 1981
- EPSTEIN-BARR-VIRUS-INDUCED LYMPHOPROLIFERATIVE DISORDER CONVERTING TO FATAL BURKITT-LIKE LYMPHOMA IN A BOY WITH INTERFERON- INDUCIBLE CHROMOSOMAL DEFECTThe Lancet, 1980
- Variation of the supercoils in closed circular DNA by binding of antibiotics and drugs: Evidence for molecular models involving intercalationJournal of Molecular Biology, 1970
- A HOMOZYGOUS CHROMOSOMAL VARIANTThe Lancet, 1969