Tedeschi B, Porfirio B, Caporossi D, Vernole P, Nicoletti B
Department of Public Health and Cell Biology, II University of Rome Tor Vergata, Italy.
Mutat Res. 1991 May;248(1):115-21. doi: 10.1016/0027-5107(91)90093-4.
Restriction endonucleases have been shown to induce chromosome damage in a variety of cultured cells. We recently reported the coincidence between MspI-induced breakage and the location of common fragile sites. We have extended our study to HpaII, which induced a 4.5-fold increase in total breakage compared to controls. It appeared that a major contribution was given by stable chromosome rearrangements, which were present at a 14-fold increased frequency in comparison to the spontaneous levels. Moreover, several chromosome bands were involved in rearrangements in different cultures from different donors. Notably, HpaII-induced breakage occurred in the same bands where breakpoints of constitutional and neoplastic rearrangements are located.
限制内切核酸酶已被证明可在多种培养细胞中诱导染色体损伤。我们最近报道了MspI诱导的断裂与常见脆性位点的位置之间的巧合。我们将研究扩展到了HpaII,与对照组相比,它使总断裂增加了4.5倍。似乎稳定的染色体重排起了主要作用,其出现频率比自发水平增加了14倍。此外,在来自不同供体的不同培养物中,有几个染色体带参与了重排。值得注意的是,HpaII诱导的断裂发生在结构重排和肿瘤性重排的断点所在的相同染色体带中。