Chadov B F
Institute of Cytology and Genetics, Russian Academy of Sciences, Novosibirsk, Russia.
Genetika. 1999 Dec;35(12):1634-42.
Analysis of the crossing over increment in the structurally normal chromosome of Drosophila caused by a rearrangement in nonhomologous chromosome (interchromosomal effect on crossing over, IEC) was carried out based on the author's personal and literature data. The IEC in the left arm of chromosome 2 caused by inversions in chromosomes X and 3, as well as the IEC in X chromosome caused by inversions in chromosomes 2 and 3, were examined. The IEC-induced increment of crossing over results from the increase of the number of double exchanges under the constant or reduced number of single exchanges. Tetrad analysis showed that the given alternation of the crossing over processes could occur only in the case of conversion of the tetrads with single exchanges into the tetrads with double exchanges. In other words, the events leading to the formation of double exchanges occur consecutively. The borders of the IEC-induced double exchanges can be seen all over the chromosome body. However, the IEC-induced increase of chromosome recombination length occurs only in the proximal region (in rare cases, in proximal and distal regions) of the chromosome arm. This means that a double exchange is formed when the first event with predominant location in the middle of the arm is supplemented with the second event predominantly localized at the arm T end, most frequently in the proximal region. The pattern of the IEC-induced double exchange formation can be satisfactorily described in terms of the contact model of the crossing over. According to the model, an elementary crossing-over event is the local contact between the homologues. Neither single exchange nor a double-stranded DNA break can serve as an elementary event in the process of any multiple exchange formation.
基于作者个人及文献数据,对由非同源染色体重排(染色体间交叉互换效应,IEC)引起的果蝇结构正常染色体交叉互换增量进行了分析。研究了X染色体和3号染色体倒位导致的2号染色体左臂的IEC,以及2号染色体和3号染色体倒位导致的X染色体的IEC。IEC诱导的交叉互换增量源于在单交换数量恒定或减少的情况下双交换数量的增加。四分体分析表明,交叉互换过程的特定交替仅在单交换四分体转变为双交换四分体的情况下才会发生。换句话说,导致双交换形成的事件是连续发生的。IEC诱导的双交换边界在染色体全长上均可观察到。然而,IEC诱导的染色体重组长度增加仅发生在染色体臂的近端区域(极少数情况下,近端和远端区域都有)。这意味着当第一个主要发生在臂中部的事件与第二个主要位于臂T端(最常见于近端区域)的事件相结合时,就会形成双交换。IEC诱导的双交换形成模式可以用交叉互换的接触模型进行令人满意的描述。根据该模型,基本的交叉互换事件是同源染色体之间的局部接触。在任何多重交换形成过程中,单交换和双链DNA断裂都不能作为基本事件。