Positional cloning of the hereditary renal carcinoma 3; 8 chromosome translocation breakpoint
Journal Article
·
· Proceedings of the National Academy of Sciences of the United States of America; (United States)
- Univ. of Colorado Cancer Center, Denver, CO (United States)
- Eleanor Roosevelt Institute, Denver, CO (United States)
- Univ. of Michigan, Ann Arbor, MI (United States)
- Harvard Medical School, Boston, MA (United States)
- Dana-Farber Cancer Institute, Boston, MA (United States)
The chromosome (p14.2;q24.1) translocation t(3;8) has been associated with hereditary renal cancer in one family. Based on cytogenetic analysis and loss-of-heterozygosity experiments, the 3p14 region has been independently implicated as harboring a tumor suppressor gene critical to kidney and lung cancer development. The 3p14.2 region also contains FRA3B, the most sensititive fragile site induced by aphidicolin. A chromosome 3 probe, R7K145, derived from a radiation-reduced hybrid was positioned between the t(3;8) breakpoint and an aphidicolin-induced 3p14 breakpoint. A yeast artificial chromosome (YAC) contig containing R7K145 was developed that crossed the aphidicolin-induced breakpoint on its telomeric side. A subsequent chromosome walk identified a YAC that crossed the 3;8 translocation breakpoint. A [lambda] sublibrary allowed isolation of clones spanning the rearrangement. Unique and evolutionarily conserved DNA sequences were used to screen a kidney cDNA library. The authors have identified a gene, referred to as HRCA1 (hereditary renal cancer associated 1), that maps immediately adjacent to the breakpoint. On the basis of its chromosomal position, HRCA1 may be a candidate tumor suppressor gene. 42 refs., 5 figs.
- OSTI ID:
- 5031413
- Journal Information:
- Proceedings of the National Academy of Sciences of the United States of America; (United States), Journal Name: Proceedings of the National Academy of Sciences of the United States of America; (United States) Vol. 90:18; ISSN PNASA6; ISSN 0027-8424
- Country of Publication:
- United States
- Language:
- English
Similar Records
Multicolor FISH mapping of YAC clones in 3p14 and identification of a YAC spanning both FRA3B and the t(3;8) associated with hereditary renal cell carcinoma
Molecular characterization of the 3p14.2 constitutive fragile site
A 350-kb cosmid contig in 3p14.2 that crosses the t(3;8) hereditary renal cell carcinoma translocation breakpoint and 17 aphidicolin-induced FRA3B breakpoints
Journal Article
·
Fri Jul 15 00:00:00 EDT 1994
· Genomics
·
OSTI ID:249989
Molecular characterization of the 3p14.2 constitutive fragile site
Journal Article
·
Thu Sep 01 00:00:00 EDT 1994
· American Journal of Human Genetics
·
OSTI ID:133736
A 350-kb cosmid contig in 3p14.2 that crosses the t(3;8) hereditary renal cell carcinoma translocation breakpoint and 17 aphidicolin-induced FRA3B breakpoints
Journal Article
·
Thu Jul 11 00:00:00 EDT 1996
· Genomics
·
OSTI ID:466022
Related Subjects
550400* -- Genetics
59 BASIC BIOLOGICAL SCIENCES
BODY
CHROMOSOMAL ABERRATIONS
CHROMOSOME BREAKAGE
CHROMOSOMES
CLONING
DISEASES
DNA HYBRIDIZATION
DNA-CLONING
GENETIC MAPPING
HEREDITARY DISEASES
HUMAN CHROMOSOME 3
HUMAN CHROMOSOME 8
HUMAN CHROMOSOMES
HYBRIDIZATION
KIDNEYS
MAPPING
MUTATIONS
NEOPLASMS
ORGANS
59 BASIC BIOLOGICAL SCIENCES
BODY
CHROMOSOMAL ABERRATIONS
CHROMOSOME BREAKAGE
CHROMOSOMES
CLONING
DISEASES
DNA HYBRIDIZATION
DNA-CLONING
GENETIC MAPPING
HEREDITARY DISEASES
HUMAN CHROMOSOME 3
HUMAN CHROMOSOME 8
HUMAN CHROMOSOMES
HYBRIDIZATION
KIDNEYS
MAPPING
MUTATIONS
NEOPLASMS
ORGANS