Dipartimento di Genetica e Biologia Molecolare, Università La Sapienza, P.le Aldo Moro 5, 00185 Roma, Italy.
Cancer Lett. 2010 Dec 18;299(1):37-44. doi: 10.1016/j.canlet.2010.08.001. Epub 2010 Sep 18.
Genome amplification is often observed in human tumors. The breakage-fusion-bridge (BFB) cycle is the mechanism that often underlies duplicated regions. Some research has indicated common fragile sites (CFS) as possible sites of chromosome breakages at the origin of BFB cycles. Here we searched two human genome regions known as amplification hot spots for any DNA copy number amplifications by analyzing 21 cancer cell lines to investigate the relationship between genomic fragility and amplification. We identified a duplicated region on a chromosomes der(2) present in the karyotype of two analysed leukemia cell lines K562. The two duplicated regions are organized into large palindromes, which suggests that one BFB cycle has occurred. Our findings show that the three breakpoints are localized in the sequence of three CFSs: FRA2H (2q32.1-q32.2), which here has been characterized molecularly; FRA2S (2q22.3-q23.3), a newly localized aphidicolin inducible CFS; and FRA2G (2q24.3-q31).
基因组扩增在人类肿瘤中经常观察到。断裂-融合-桥(BFB)循环是导致重复区域的常见机制。一些研究表明,常见脆弱位点(CFS)可能是 BFB 循环起源处染色体断裂的位置。在这里,我们通过分析 21 种癌细胞系,在两个已知的人类基因组扩增热点区域中搜索任何 DNA 拷贝数扩增,以研究基因组脆性与扩增之间的关系。我们在两个分析的白血病细胞系 K562 的核型中发现了染色体 der(2)上的一个重复区域。这两个重复区域被组织成大型回文结构,这表明发生了一个 BFB 循环。我们的研究结果表明,三个断点定位于三个 CFS 序列中:FRA2H(2q32.1-q32.2),在这里已经进行了分子特征描述;FRA2S(2q22.3-q23.3),一个新定位的吖啶酮诱导的 CFS;和 FRA2G(2q24.3-q31)。