Ma C, Martin S, Trask B, Hamlin J L
Department of Biochemistry, University of Virginia School of Medicine, Charlottesville 22908.
Genes Dev. 1993 Apr;7(4):605-20. doi: 10.1101/gad.7.4.605.
We have utilized a dihydrofolate reductase (DHFR) probe in combination with selected probes from other positions along the 2q chromosome arm in a two-color fluorescence in situ hybridization analysis of early DHFR gene amplification events in CHO cells. These studies show clearly that the most frequent initiating event is the formation of a giant inverted duplication, resulting from chromosome breakage and terminal fusion or a reverse unequal sister chromatid exchange. The dicentric chromosomes thus formed initiate bridge/breakage/fusion cycles that appear to mediate subsequent amplification steps to higher copy number.
我们运用二氢叶酸还原酶(DHFR)探针,并结合来自2号染色体长臂其他位置的特定探针,对CHO细胞早期DHFR基因扩增事件进行双色荧光原位杂交分析。这些研究清楚地表明,最常见的起始事件是形成巨大的反向重复,这是由染色体断裂和末端融合或反向不等姐妹染色单体交换导致的。如此形成的双着丝粒染色体启动桥/断裂/融合循环,这似乎介导了随后向更高拷贝数的扩增步骤。