Preston C R, Engels W R
Laboratory of Genetics, University of Wisconsin, Madison 53706, USA.
Genetics. 1996 Dec;144(4):1611-22. doi: 10.1093/genetics/144.4.1611.
A P-element insertion flanked by 13 restriction fragment length polymorphism (RFLP) marker sites was used to examine male recombination and gene conversion at an autosomal site. The great majority of crossovers on chromosome arm 2R occurred within the 4-kb region containing the P element and RFLP sites. Of the 128 recombinants analyzed, approximately two-thirds carried duplications or deletions flanking the P element. These rearrangements are described in more detail in the accompanying report. In a parallel experiment, we examined 91 gene conversion tracts resulting from excision of the same autosomal P element. We found the average tract length was 1463 bp, which is essentially the same as found previously at the white locus. The distribution of conversion tract endpoints was indistinguishable from the distribution of crossover points among the nonrearranged male recombinants. Most recombination events can be explained by the "hybrid element insertion" model, but, for those lacking a duplication or deletion, a second step involving double-strand gap repair must be postulated to explain the distribution of crossover points.
一个两侧带有13个限制性片段长度多态性(RFLP)标记位点的P因子插入片段被用于检测常染色体位点处的雄性重组和基因转换。2R染色体臂上的绝大多数交叉发生在包含P因子和RFLP位点的4kb区域内。在分析的128个重组体中,约三分之二携带P因子两侧的重复或缺失。这些重排在随附报告中有更详细的描述。在一个平行实验中,我们检测了由同一个常染色体P因子切除产生的91个基因转换片段。我们发现平均片段长度为1463bp,这与之前在白眼基因座处发现的基本相同。转换片段端点的分布与未重排的雄性重组体中交叉点的分布没有区别。大多数重组事件可以用“杂种元件插入”模型来解释,但是,对于那些没有重复或缺失的重组事件,必须假定第二步涉及双链缺口修复来解释交叉点的分布。