Molecular characterization of a large homozygous deletion in the small cell lung cancer cell line U2020: A strategy for cloning the putative tumor suppressor gene
- 1 September 1992
- journal article
- research article
- Published by Wiley in Genes, Chromosomes and Cancer
- Vol. 5 (2) , 119-127
- https://doi.org/10.1002/gcc.2870050205
Abstract
Homozygous deletions are instrumental in the detection and cloning of tumor suppressor genes. We report the isolation and characterization of 39 new single‐copy probes saturating a submicroscopic homozygous deletion detected in the DNA of the small cell lung cancer (SCLC) cell line U2020. The probes were selected from a large collection, covering the entire length of chromosome 3 with an estimated average spacing of 100–150 kb. Based on the number of probes in the deletion and the probe density, the size of the U2020 submicroscopic deletion was estimated to be in the range of 4–7 megabases. Among the deleted loci, 17 showed conservation across species, probably representing potential coding gene sequences. By genetic and physical mapping of a large randomly chosen fraction of the deleted probes, we defined the location of the U2020 deletion within chromosome band 3p 12. Our cloning strategy is based on narrowing the region of interest by eliminating probes that retain heterozygosity in SCLC samples, thus selecting for probes in the region of common loss.Keywords
This publication has 14 references indexed in Scilit:
- Involvement of the RAFI locus, at band 3p25, in the 3p deletion of small‐cell lung cancerGenes, Chromosomes and Cancer, 1991
- Isolation and regional localization of a large collection (2,000) of single-copy DNA fragments on human chromosome 3 for mapping and cloning tumor suppressor genesHuman Genetics, 1991
- Gene deletions causing human genetic disease: mechanisms of mutagenesis and the role of the local DNA sequence environmentHuman Genetics, 1991
- Tumor suppressor genesCell, 1991
- Localization of polymorphic DNA probes frequently deleted in lung carcinomaHuman Genetics, 1989
- Sensitive, high-resolution chromatin and chromosome mapping in situ: Presence and orientation of two closely integrated copies of EBV in a lymphoma lineCell, 1988
- Use of whole cosmid cloned genomic sequences for chromosomal localization by non-radioactive in situ hybridizationHuman Genetics, 1987
- Construction of multilocus genetic linkage maps in humans.Proceedings of the National Academy of Sciences, 1987
- Kpn I family of long interspersed repeated DNA sequences in primates: polymorphism of family members and evidence for transcription.Proceedings of the National Academy of Sciences, 1983
- Mutation and Cancer: Statistical Study of RetinoblastomaProceedings of the National Academy of Sciences, 1971