Nalbantoglu J, Hartley D, Phear G, Tear G, Meuth M
EMBO J. 1986 Jun;5(6):1199-204. doi: 10.1002/j.1460-2075.1986.tb04347.x.
To examine the factors governing the generation of DNA sequence rearrangements in mammalian somatic cells, we have cloned and sequenced novel junctions produced by six spontaneous deletion mutations at the aprt locus of Chinese hamster ovary cells. Our analyses indicate that these rearrangements were produced by non-homologous recombinational events occurring between short (2-7 bp) sequence repeats at the two termini of the deletion which leave one copy of the repeat in the mutant gene. Certain tri- and tetranucleotides recur at the deletion termini, suggesting that these may possibly be a recognition sequence for an enzyme involved in the event. No other gene structural alterations were found at the novel junctions or in neighbouring sequences. The deletions are not randomly distributed over the aprt gene; four termini clustered in a 40-bp sequence. This region of aprt is unusual as it contains both significant stretches of dyad symmetry which could potentially form stable DNA secondary structures and short direct repeats. Regions of dyad symmetry were also found at at least one terminus of all the deletions. In view of the similar properties of this set of deletions, possible mechanisms for the formation of this type of gene rearrangement are considered.
为了研究哺乳动物体细胞中DNA序列重排产生的调控因素,我们克隆并测序了中国仓鼠卵巢细胞aprt基因座上六个自发缺失突变产生的新连接点。我们的分析表明,这些重排是由缺失两端短(2 - 7 bp)序列重复之间发生的非同源重组事件产生的,这些重复序列在突变基因中留下一个拷贝。某些三核苷酸和四核苷酸在缺失末端反复出现,这表明它们可能是参与该事件的酶的识别序列。在新连接点或相邻序列中未发现其他基因结构改变。这些缺失并非随机分布在aprt基因上;四个末端聚集在一个40 bp的序列中。aprt的这个区域很不寻常,因为它既包含可能形成稳定DNA二级结构的显著的二分对称序列,又包含短的直接重复序列。在所有缺失的至少一个末端也发现了二分对称区域。鉴于这组缺失的相似特性,我们考虑了这种类型基因重排形成的可能机制。