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粒细胞-巨噬细胞集落刺激因子(GM-CSF)和FMS参与骨髓疾病中5号染色体长臂缺失(5q)的证据。

Evidence for the involvement of GM-CSF and FMS in the deletion (5q) in myeloid disorders.

作者信息

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

出版信息

Science. 1986 Feb 28;231(4741):984-7. doi: 10.1126/science.3484837.

Abstract

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.

摘要

通过原位染色体杂交,GM - CSF基因和FMS基因分别定位于人类5号染色体的q23至q31带以及5q33带。这些基因编码参与造血调节的蛋白质,且位于肿瘤性髓系疾病患者中经常缺失的染色体区域内。两名患有难治性贫血且有del(5)(q15q33.3)的患者骨髓细胞中的5号染色体长臂缺失,这两个基因均被删除。在第三名患有急性非淋巴细胞白血病(ANLL)且缺失较小,为del(5)(q22q33.1)的患者中,仅GM - CSF基因被删除。来自第四名患有ANLL且没有5号染色体长臂缺失,但有一条重排的5号染色体缺失q31.3至q33.1带[ins(21;5)(q22;q31.3q33.1)]的患者的白血病细胞被用于这些基因的亚定位;两个基因都存在于重排的5号染色体上。因此,这些基因中的一个或两个的缺失可能在骨髓增生异常综合征或ANLL的发病机制中起重要作用。

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