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人类c-fms原癌基因在造血细胞中的表达及其在5q-综合征中的缺失。

Expression of the human c-fms proto-oncogene in hematopoietic cells and its deletion in the 5q- syndrome.

作者信息

Nienhuis A W, Bunn H F, Turner P H, Gopal T V, Nash W G, O'Brien S J, Sherr C J

出版信息

Cell. 1985 Sep;42(2):421-8. doi: 10.1016/0092-8674(85)90099-6.

Abstract

The c-fms proto-oncogene was shown to be expressed in human bone marrow and in differentiated blood mononuclear cells, suggesting that its gene product plays a role in hematopoietic maturation. The c-fms mRNA was not detected in HL-60 cells, an established promyelocytic line, whereas c-fms expression appeared 48 hr after induction when most cells had differentiated into macrophages. An acquired deletion of chromosome 5 (5q-) in bone marrow cells is associated with abnormalities in blood cell production. The normal 5 and 5q- chromosomes were segregated by construction of cell hybrids between bone marrow and rodent cells. A selective system was used that requires retention of the structural gene for dihydrofolate reductase, located on human chromosome 5. Analysis of DNA from individual hybrid clones revealed that the 5q- deletion had removed the c-fms gene. We postulate that hemizygosity at the c-fms locus leads to abnormalities in hematopoietic maturation.

摘要

c-fms原癌基因已被证明在人类骨髓和分化的血液单核细胞中表达,这表明其基因产物在造血成熟过程中发挥作用。在已建立的早幼粒细胞系HL-60细胞中未检测到c-fms mRNA,而在诱导48小时后,当大多数细胞已分化为巨噬细胞时,c-fms表达出现。骨髓细胞中5号染色体(5q-)的获得性缺失与血细胞生成异常有关。通过构建骨髓细胞与啮齿动物细胞之间的细胞杂种,将正常的5号染色体和5q-染色体进行了分离。使用了一种选择性系统,该系统需要保留位于人类5号染色体上的二氢叶酸还原酶结构基因。对单个杂种克隆的DNA分析表明,5q-缺失已去除了c-fms基因。我们推测,c-fms基因座的半合子状态会导致造血成熟异常。

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