VanHulle Kelly, Lemoine Francene J, Narayanan Vidhya, Downing Brandon, Hull Krista, McCullough Christy, Bellinger Melissa, Lobachev Kirill, Petes Thomas D, Malkova Anna
Biology Department, Indiana University/Purdue University Indiana, 723 West Michigan Street, Indianapolis, IN 46202-5132, USA.
Mol Cell Biol. 2007 Apr;27(7):2601-14. doi: 10.1128/MCB.01740-06. Epub 2007 Jan 22.
Inverted DNA repeats are known to cause genomic instabilities. Here we demonstrate that double-strand DNA breaks (DSBs) introduced a large distance from inverted repeats in the yeast (Saccharomyces cerevisiae) chromosome lead to a burst of genomic instability. Inverted repeats located as far as 21 kb from each other caused chromosome rearrangements in response to a single DSB. We demonstrate that the DSB initiates a pairing interaction between inverted repeats, resulting in the formation of large dicentric inverted dimers. Furthermore, we observed that propagation of cells containing inverted dimers led to gross chromosomal rearrangements, including translocations, truncations, and amplifications. Finally, our data suggest that break-induced replication is responsible for the formation of translocations resulting from anaphase breakage of inverted dimers. We propose a model explaining the formation of inverted dicentric dimers by intermolecular single-strand annealing (SSA) between inverted DNA repeats. According to this model, anaphase breakage of inverted dicentric dimers leads to gross chromosomal rearrangements (GCR). This "SSA-GCR" pathway is likely to be important in the repair of isochromatid breaks resulting from collapsed replication forks, certain types of radiation, or telomere aberrations that mimic isochromatid breaks.
已知反向DNA重复序列会导致基因组不稳定。在此我们证明,在酵母(酿酒酵母)染色体中距反向重复序列很远的位置引入的双链DNA断裂(DSB)会引发一阵基因组不稳定。相距达21 kb的反向重复序列会因单个DSB而导致染色体重排。我们证明DSB引发了反向重复序列之间的配对相互作用,导致形成大型双着丝粒反向二聚体。此外,我们观察到含有反向二聚体的细胞的增殖会导致大规模染色体重排,包括易位、截短和扩增。最后,我们的数据表明断裂诱导复制是由反向二聚体后期断裂导致的易位形成的原因。我们提出了一个模型,解释通过反向DNA重复序列之间的分子间单链退火(SSA)形成反向双着丝粒二聚体的过程。根据这个模型,反向双着丝粒二聚体的后期断裂会导致大规模染色体重排(GCR)。这种“SSA-GCR”途径可能在修复由复制叉塌陷、某些类型的辐射或模拟等臂染色单体断裂的端粒畸变导致的等臂染色单体断裂中起重要作用。