生物
分子生物学
核型
染色
染色体易位
染色体
癌变
标记染色体
癌基因
N-Myc公司
基因复制
基因
细胞培养
遗传学
神经母细胞瘤
细胞周期
神经节细胞瘤
作者
Kari Alitalo,M. Schwab,Ching‐Shwun Lin,Harold Varmus,J. Michael Bishop
标识
DOI:10.1073/pnas.80.6.1707
摘要
Two human neuroendocrine tumor cell lines derived from a colon carcinoma contain either numerous double minute chromosomes (COLO 320 DM) or a homogeneously staining marker chromosome (COLO 320 HSR). We found amplification and enhanced expression of the cellular oncogene c-myc in both COLO 320 DM and HSR cells, and we were able to show that the homogeneously staining regions of the COLO 320 HSR marker chromosome contain amplified c-myc. From previous and present karyotypes, it appears that the homogeneously staining regions reside on a distorted X chromosome. Therefore, amplification of c-myc has been accompanied by translocation of the gene from its normal position on chromosome 8 (8q24). Because double minute chromosomes were features of primary cultures from the original tumor, it seems reasonable to suspect that amplification of c-myc may have contributed to tumorigenesis.
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