Smith Gerald R
Division of Basic Sciences, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
Cell. 2004 Apr 16;117(2):146-8. doi: 10.1016/s0092-8674(04)00338-1.
Views of how homologous recombination is initiated have changed over the past several decades: in the 1960s and 1970s, single-strand DNA lesions (nicks) were the leading contenders, but in the last decade, double-strand DNA breaks (DSBs) have reigned. In this issue of Cell, evidence is presented that nicks can stimulate homologous recombination and, in uncontrolled situations, may lead to translocations and other potentially dangerous genome rearrangements.
在过去几十年里,关于同源重组如何起始的观点发生了变化:在20世纪60年代和70年代,单链DNA损伤(切口)是主要的候选因素,但在过去十年中,双链DNA断裂(DSB)占据了主导地位。在本期《细胞》杂志中,有证据表明切口可以刺激同源重组,并且在不受控制的情况下,可能导致易位和其他潜在危险的基因组重排。