Bzymek M, Lovett S T
Department of Biology, Brandeis University, 415 South Street, Waltham, MA 02454-9110, USA.
Proc Natl Acad Sci U S A. 2001 Jul 17;98(15):8319-25. doi: 10.1073/pnas.111008398.
Rearrangements between tandem sequence homologies of various lengths are a major source of genomic change and can be deleterious to the organism. These rearrangements can result in either deletion or duplication of genetic material flanked by direct sequence repeats. Molecular genetic analysis of repetitive sequence instability in Escherichia coli has provided several clues to the underlying mechanisms of these rearrangements. We present evidence for three mechanisms of RecA-independent sequence rearrangements: simple replication slippage, sister-chromosome exchange-associated slippage, and single-strand annealing. We discuss the constraints of these mechanisms and contrast their properties with RecA-dependent homologous recombination. Replication plays a critical role in the two slipped misalignment mechanisms, and difficulties in replication appear to trigger rearrangements via all these mechanisms.
不同长度串联序列同源性之间的重排是基因组变化的主要来源,可能对生物体有害。这些重排可导致由直接序列重复序列侧翼的遗传物质缺失或重复。对大肠杆菌中重复序列不稳定性的分子遗传学分析为这些重排的潜在机制提供了一些线索。我们提供了三种不依赖RecA的序列重排机制的证据:简单复制滑移、姐妹染色单体交换相关滑移和单链退火。我们讨论了这些机制的限制,并将它们的特性与依赖RecA的同源重组进行了对比。复制在两种滑移错配机制中起关键作用,复制困难似乎通过所有这些机制触发重排。