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  • 1
    Publication Date: 1986-01-17
    Description: Gene probes for interferons alpha and beta 1 and v-ets were hybridized to metaphase chromosomes from three patients with acute monocytic leukemia who had a chromosomal translocation, t(9;11)(p22;q23). The break in the short arm of chromosome 9 split the interferon genes, and the interferon-beta 1 gene was translocated to chromosome 11. The c-ets-1 gene was translocated from chromosome 11 to the short arm of chromosome 9 adjacent to the interferon genes. No DNA rearrangement was observed when these probes were hybridized to genomic DNA from leukemic cells of two of the patients. The results suggest that the juxtaposition of the interferon and c-ets-1 genes may be involved in the pathogenesis of human monocytic leukemia.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Diaz, M O -- Le Beau, M M -- Pitha, P -- Rowley, J D -- CA 16910/CA/NCI NIH HHS/ -- New York, N.Y. -- Science. 1986 Jan 17;231(4735):265-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3455787" target="_blank"〉PubMed〈/a〉
    Keywords: Chromosome Mapping ; Chromosomes, Human, 6-12 and X ; DNA, Neoplasm/genetics ; Humans ; Interferon Type I/*genetics ; Leukemia, Monocytic, Acute/*genetics ; Nucleic Acid Hybridization ; *Proto-Oncogenes ; *Translocation, Genetic
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 2
    Publication Date: 1986-02-28
    Description: By in situ chromosomal hybridization, the GM-CSF and FMS genes were localized to human chromosome 5 at bands q23 to q31, and at band 5q33, respectively. These genes encode proteins involved in the regulation of hematopoiesis, and are located within a chromosome region frequently deleted in patients with neoplastic myeloid disorders. Both genes were deleted in the 5q-chromosome from bone marrow cells of two patients with refractory anemia and a del(5)(q15q33.3). The GM-CSF gene alone was deleted in a third patient with acute nonlymphocytic leukemia (ANLL) who has a smaller deletion, del(5)(q22q33.1). Leukemia cells from a fourth patient who has ANLL and does not have a del(5q), but who has a rearranged chromosome 5 that is missing bands q31.3 to q33.1 [ins(21;5)(q22;q31.3q33.1)] were used to sublocalize these genes; both genes were present on the rearranged chromosome 5. Thus, the deletion of one or both of these genes may be important in the pathogenesis of myelodysplastic syndromes or of ANLL.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Le Beau, M M -- Westbrook, C A -- Diaz, M O -- Larson, R A -- Rowley, J D -- Gasson, J C -- Golde, D W -- Sherr, C J -- CA 16910/CA/NCI NIH HHS/ -- CA 23954/CA/NCI NIH HHS/ -- CA 30388/CA/NCI NIH HHS/ -- etc. -- New York, N.Y. -- Science. 1986 Feb 28;231(4741):984-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3484837" target="_blank"〉PubMed〈/a〉
    Keywords: Anemia, Refractory/genetics ; Bone Marrow Diseases/*genetics ; *Chromosome Deletion ; Chromosome Mapping ; *Chromosomes, Human, 4-5 ; Colony-Stimulating Factors/*genetics ; Humans ; Leukemia/genetics ; *Proto-Oncogenes
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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