Preston C R, Sved J A, Engels W R
Laboratory of Genetics, University of Wisconsin, Madison 53706, USA.
Genetics. 1996 Dec;144(4):1623-38. doi: 10.1093/genetics/144.4.1623.
We studied P element-induced recombination in germline mitotic cells by examining the structure of the recombinant chromosomes. We found that most recombinants retain a mobile P element at the site of the recombination, usually with either a deletion or a duplication immediately adjacent to the P end at which the crossover occurred. The sizes of these deletions and duplications ranged from a few base pairs to well over 100 kb. These structures fit the "hybrid element insertion" (HEI) model of male recombination in which the two P-element copies on sister chromatids combine to form a "hybrid element" whose termini insert into a nearby position on the homologue. The data suggest that P-induced recombination can be used as an efficient means of generating flanking deletions in the vicinity of existing P elements. These deletions are easily screened using distant flanking markers, and they can be chosen to extend in a given direction depending on which reciprocal recombinant type is selected. Furthermore, the retention of a mobile P element allows one to extend the deletion or generate additional variability at the site by subsequent rounds of recombination.
我们通过检查重组染色体的结构来研究种系有丝分裂细胞中P因子诱导的重组。我们发现,大多数重组体在重组位点保留了一个可移动的P因子,通常在发生交叉的P末端紧邻处有一个缺失或重复。这些缺失和重复的大小从几个碱基对到超过100 kb不等。这些结构符合雄性重组的“杂交元件插入”(HEI)模型,即姐妹染色单体上的两个P因子拷贝结合形成一个“杂交元件”,其末端插入同源染色体上的附近位置。数据表明,P因子诱导的重组可以作为在现有P因子附近产生侧翼缺失的有效方法。使用远距离侧翼标记很容易筛选这些缺失,并且可以根据选择的哪种相互重组类型选择在给定方向上延伸。此外,保留一个可移动的P因子允许通过后续的重组轮次扩展缺失或在该位点产生额外的变异性。