Frequent loss of heterozygosity at the MCC locus on chromosome 5q21-22 in sporadic colorectal carcinomas. 1991

Y Miki, and I Nishisho, and Y Miyoshi, and A Horii, and H Ando, and T Nakajima, and J Utsunomiya, and Y Nakamura
Department of Biochemistry, Cancer Institute, Tokyo.

Recent studies have identified a gene on chromosome 5q, designated MCC (mutated in colorectal cancers), as a candidate for the putative colorectal tumor suppressor gene that is located at 5q21. We examined loss of heterozygosity (LOH) at the MCC locus and its vicinity in sporadic colorectal carcinomas, using 12 RFLP (restriction fragment length polymorphism) markers. One clone, L5.71, had been used to identify the MCC gene; all 12 markers also had tight linkage to the gene responsible for adenomatous polyposis coli. All 40 cases studied were informative with at least one marker, and 22 of them (55%) showed LOH at one or more loci. LOH in the tumors was more frequent in the immediate vicinity of L5.71 than in distant parts of the chromosome, and a common region of deletion was detected between markers L5.62 and 15A6. In one case, alleles were retained at L5.71 and at loci proximal to L5.71, but alleles were lost at loci distal to L5.71. In another case, both alleles were retained at L5.71 but alleles were lost at loci proximal and distal to L5.71. These results support the conclusion that a tumor suppressor gene for colorectal carcinoma is located within or around locus L5.71.

UI MeSH Term Description Entries
D012150 Polymorphism, Restriction Fragment Length Variation occurring within a species in the presence or length of DNA fragment generated by a specific endonuclease at a specific site in the genome. Such variations are generated by mutations that create or abolish recognition sites for these enzymes or change the length of the fragment. RFLP,Restriction Fragment Length Polymorphism,RFLPs,Restriction Fragment Length Polymorphisms
D002874 Chromosome Mapping Any method used for determining the location of and relative distances between genes on a chromosome. Gene Mapping,Linkage Mapping,Genome Mapping,Chromosome Mappings,Gene Mappings,Genome Mappings,Linkage Mappings,Mapping, Chromosome,Mapping, Gene,Mapping, Genome,Mapping, Linkage,Mappings, Chromosome,Mappings, Gene,Mappings, Genome,Mappings, Linkage
D002895 Chromosomes, Human, Pair 5 One of the two pairs of human chromosomes in the group B class (CHROMOSOMES, HUMAN, 4-5). Chromosome 5
D004273 DNA, Neoplasm DNA present in neoplastic tissue. Neoplasm DNA
D006579 Heterozygote An individual having different alleles at one or more loci regarding a specific character. Carriers, Genetic,Genetic Carriers,Carrier, Genetic,Genetic Carrier,Heterozygotes
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D015179 Colorectal Neoplasms Tumors or cancer of the COLON or the RECTUM or both. Risk factors for colorectal cancer include chronic ULCERATIVE COLITIS; FAMILIAL POLYPOSIS COLI; exposure to ASBESTOS; and irradiation of the CERVIX UTERI. Colorectal Cancer,Colorectal Carcinoma,Colorectal Tumors,Neoplasms, Colorectal,Cancer, Colorectal,Cancers, Colorectal,Carcinoma, Colorectal,Carcinomas, Colorectal,Colorectal Cancers,Colorectal Carcinomas,Colorectal Neoplasm,Colorectal Tumor,Neoplasm, Colorectal,Tumor, Colorectal,Tumors, Colorectal
D016153 Genes, Suppressor Genes that have a suppressor allele or suppressor mutation (SUPPRESSION, GENETIC) which cancels the effect of a previous mutation, enabling the wild-type phenotype to be maintained or partially restored. For example, amber suppressors cancel the effect of an AMBER NONSENSE MUTATION. Amber Suppressor Genes,Frameshift Suppressor Genes,Genes, Amber Suppressor,Genes, Frameshift Suppressor,Genes, Nonsense Mutation Suppressor,Genes, Ochre Suppressor,Genes, Second-Site Suppressor,Nonsense Mutation Suppressor Genes,Ochre Suppressor Genes,Second-Site Suppressor Genes,Genes, Opal Suppressor,Suppressor Genes,Amber Suppressor Gene,Frameshift Suppressor Gene,Gene, Amber Suppressor,Gene, Frameshift Suppressor,Gene, Ochre Suppressor,Gene, Opal Suppressor,Gene, Second-Site Suppressor,Gene, Suppressor,Genes, Second Site Suppressor,Ochre Suppressor Gene,Opal Suppressor Gene,Opal Suppressor Genes,Second Site Suppressor Genes,Second-Site Suppressor Gene,Suppressor Gene,Suppressor Gene, Amber,Suppressor Gene, Frameshift,Suppressor Gene, Ochre,Suppressor Gene, Opal,Suppressor Gene, Second-Site,Suppressor Genes, Amber,Suppressor Genes, Frameshift,Suppressor Genes, Ochre,Suppressor Genes, Opal,Suppressor Genes, Second-Site

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