Nassif N, Penney J, Pal S, Engels W R, Gloor G B
Laboratory of Genetics, University of Wisconsin--Madison 53706.
Mol Cell Biol. 1994 Mar;14(3):1613-25. doi: 10.1128/mcb.14.3.1613-1625.1994.
P-element-induced gap repair was used to copy nonhomologous DNA into the Drosophila white locus. We found that nearly 8,000 bp of nonhomologous sequence could be copied from an ectopic template at essentially the same rate as a single-base substitution at the same location. An in vitro-constructed deletion was also copied into white at high frequencies. This procedure can be applied to the study of gene expression in Drosophila melanogaster, especially for genes too large to be manipulated in other ways. We also observed several types of more complex events in which the copied template sequences were rearranged such that the breakpoints occurred at direct duplications. Most of these can be explained by a model of double strand break repair in which each terminus of the break invades a template independently and serves as a primer for DNA synthesis from it, yielding two overlapping single-stranded sequences. These single strands then pair, and synthesis is completed by each using the other as a template. This synthesis-dependent strand annealing (SDSA) model as a possible general mechanism in complex organisms is discussed.
利用P因子诱导的缺口修复将非同源DNA复制到果蝇的白眼基因座中。我们发现,近8000 bp的非同源序列能够以与同一位置单碱基替换基本相同的速率从异位模板进行复制。体外构建的缺失片段也能以高频复制到白眼基因中。该方法可应用于黑腹果蝇基因表达的研究,尤其适用于那些因太大而无法用其他方法操作的基因。我们还观察到几种更复杂的事件,其中复制的模板序列发生重排,使得断点出现在同向重复处。这些事件大多可以用双链断裂修复模型来解释,即断裂的每个末端独立侵入一个模板,并作为从该模板进行DNA合成的引物,产生两个重叠的单链序列。然后这些单链配对,各自以对方为模板完成合成。本文讨论了合成依赖链退火(SDSA)模型作为复杂生物体中一种可能的普遍机制。