Hastings P J
Department of Genetics, University of Alberta, Edmonton, Canada.
Mutat Res. 1992 Dec 1;284(1):97-110. doi: 10.1016/0027-5107(92)90026-x.
In fungi, most mitotic recombination and at least some meiotic recombination appear to stem from a process of double-strand break repair. During this repair, recombination occurs by conversion caused by the process of double-strand gap filling, by conversion related to heteroduplex formation where homologous molecules interact by complementary base pairing, and by crossing-over which is probably an occasional byproduct of the repair process. From a review of the genetic and biochemical data and the published models of the process of recombination, the following view emerges: broken ends may be acted upon by nucleases and helicases to produce a recombinagenic end which may have both 3' and 5' single-stranded tails. These postulated split-ends may then act independently to find regions of homology with which to react. Invasion by both ends forms two splice-junctions which prime DNA synthesis towards each other to replace lost information, using the homologous sequences as templates. This process would lead to a structure which consists of a double Holliday junction which may be resolved endonucleolytically, sometimes giving a crossover, or by another means such as the action of topoisomerase, to dissolve the structure without a crossover having been formed.
在真菌中,大多数有丝分裂重组以及至少一些减数分裂重组似乎源于双链断裂修复过程。在这种修复过程中,重组通过双链缺口填补过程引起的转换、与异源双链形成相关的转换(其中同源分子通过互补碱基配对相互作用)以及可能是修复过程偶尔产生的副产物的交叉互换而发生。从对重组过程的遗传和生化数据以及已发表模型的综述中,出现了以下观点:断裂末端可能会被核酸酶和解旋酶作用,产生一个可能具有3'和5'单链尾巴的重组性末端。这些假定的裂端然后可能独立起作用,寻找与之反应的同源区域。两端的侵入形成两个剪接连接点,以同源序列为模板,向彼此引导DNA合成以取代丢失的信息。这个过程将导致形成一个由双Holliday连接点组成的结构,该结构可以通过核酸内切酶分解,有时会产生交叉互换,或者通过另一种方式,如拓扑异构酶的作用,在不形成交叉互换的情况下溶解该结构。