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Publication : Human and mouse cellular myc protooncogenes reside on chromosomes involved in numerical and structural aberrations in cancer.

First Author  Sakaguchi AY Year  1983
Journal  Somatic Cell Genet Volume  9
Issue  3 Pages  391-405
PubMed ID  6857448 Mgi Jnum  J:7087
Mgi Id  MGI:55558 Doi  10.1007/BF01539146
Citation  Sakaguchi AY, et al. (1983) Human and mouse cellular myc protooncogenes reside on chromosomes involved in numerical and structural aberrations in cancer. Somatic Cell Genet 9(3):391-405
abstractText  A molecular clone of viral myc (v-myc), the oncogene of avian myelocytomatosis virus, MC29, detected homologous human, mouse, and Chinese hamster cellular myc (c-myc) sequences by Southern filter hybridization. A v-myc probe, containing sequences from the 3' domain of the gene, hybridized to single human HindIII and mouse EcoRI genomic DNA fragments of the cellular myc genes whose segregation could be followed in interspecies somatic cell hybrids. Human c-myc segregated concordantly with the enzyme marker glutathione reductase and with a karyotypically normal chromosome 8. A rearrangement of human c-myc was observed in Burkitt's lymphoma cells possessing the t(8;14) translocation. These results suggest that human c-myc is located close to the breakpoint on chromosome 8 (q24) involved in the t(8;14) translocation. The mouse c-myc gene segregated concordantly with chromosome 15 in mouse-Chinese hamster cell hybrids. These gene assignments are noteworthy, as structural and numerical abnormalities of human chromosome 8 and mouse chromosome 15 are associated frequently with B-cell neoplasms.
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