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Excision of N-myc from chromosome 2 in human neuroblastoma cells containing amplified N-myc sequences.

机译:在含有扩增的N-myc序列的人神经母细胞瘤细胞中从2号染色体切除N-myc。

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摘要

Amplification of one of three growth-stimulating myc genes is a common method by which many tumor types gain a proliferative advantage. In metastatic human neuroblastoma, the amplification of the N-myc locus, located on chromosome 2, is a dominant feature of this usually fatal pediatric cancer. Of the many models proposed to explain this amplification, all incorporate as the initial step either disproportionate overreplication of the chromosomal site or recombination across a loop structure. The original locus is retained within the chromosome in the overreplication models but is excised in the recombination models. To test these models, we have used somatic cell hybrids to separate and analyze the chromosomes 2 from a neuroblastoma cell line containing in vivo amplified N-myc. Our results demonstrate that N-myc is excised from one of the chromosomes, suggesting that deletion is a requisite part of gene amplification in a naturally occurring system.
机译:三种生长刺激性myc基因之一的扩增是一种常见的方法,许多肿瘤类型可通过这种方法获得增殖优势。在转移性人类神经母细胞瘤中,位于2号染色体上的N-myc基因座的扩增是这种通常致命的儿科癌症的主要特征。在提议用来解释这种扩增的许多模型中,所有模型都将不成比例的染色体位点过度复制或跨环结构重组作为初始步骤。原始基因座在过度复制模型中保留在染色体内,但在重组模型中被切除。为了测试这些模型,我们使用了体细胞杂种从包含体内扩增的N-myc的神经母细胞瘤细胞系中分离并分析了2号染色体。我们的结果表明,N-myc是从其中一条染色体上切除的,这表明缺失是自然发生系统中基因扩增的必要部分。

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