Munz P L, Young C S
Virology. 1984 Jun;135(2):503-14. doi: 10.1016/0042-6822(84)90204-6.
The distributions of the crossovers necessary to generate ts+ genomes have been examined in a collection of clonally unrelated ts+ recombinants from a set of ts X ts adenovirus crosses. In a cross between two parents that are grossly heterologous between map units 80.2 and 91.5, the distribution of crossovers was significantly skewed toward the left-hand end of the genome, with a declining frequency proceeding rightward. This gradient of recombination was modified by the removal of the right-hand heterology and by the presence of another region of heterology between map units 3.67 and 10.11. In a cross where the ts markers were flanked by both heterologies, no gradient was observed and ts+ recombinants were characterized by a higher rate of supernumerary crossovers. In a cross designed so that one ts marker was internal to two heterologies, crossovers were found disproportionately between the second ts marker and the nearby heterology. In addition, ts+ recombinants formed by crossing over internal to the heterologies again were accompanied by a high frequency of supernumerary crossovers. Finally, ts+ recombinant frequencies in crosses identical except for the presence of either one or two flanking heterologies were markedly lower in the latter case. These data, taken together, suggest that a major pathway of adenovirus recombination initiates at, or near, the molecular termini and is perhaps driven by the displaced single strands produced during DNA replication. Internal initiation, on the other hand, may employ these single strands to form genetic "patches."
在一组ts×ts腺病毒杂交产生的一系列克隆无关的ts+重组体中,研究了产生ts+基因组所需交换的分布情况。在两个亲本之间的杂交中,这两个亲本在图谱单位80.2和91.5之间存在明显的异源区域,交换的分布明显偏向基因组的左端,频率向右逐渐下降。通过去除右端异源区域以及在图谱单位3.67和10.11之间存在另一个异源区域,改变了这种重组梯度。在一个杂交中,ts标记两侧都有异源区域,未观察到梯度,并且ts+重组体的特征是额外交换的发生率较高。在一个设计的杂交中,使一个ts标记位于两个异源区域内部,在第二个ts标记和附近的异源区域之间发现交换不成比例。此外,通过在异源区域内部发生交换形成的ts+重组体再次伴随着高频的额外交换。最后,除了存在一个或两个侧翼异源区域外其他相同的杂交中,ts+重组频率在后一种情况下明显较低。综合这些数据表明,腺病毒重组的主要途径在分子末端或其附近起始,可能由DNA复制过程中产生的置换单链驱动。另一方面,内部起始可能利用这些单链形成遗传“补丁”。