Beck B N
Genetics. 1980 Sep;96(1):25-41. doi: 10.1093/genetics/96.1.25.
The process of close recombinant formation in bacteriophage T5 crosses has been studied by examining the structure of internal heterozygotes (HETs), the immediate products of recombination events. The T5 system was chosen because it permits the study of internal heterozygotes exclusively, thus avoiding the ambiguities inherent in previous studies with T4. The heterozygotes were obtained by the nonselective screening of progeny phage in a prematurely lysed sample from an eight-factor cross. The molecular structure of each HET was inferred from the strand genotypes displayed among its progeny. This investigation presents unequivocal evidence that both overlap and insertion HETs are intermediates in recombinant formation and that insertion HETs are a significant source of close double recombinants. There is evidence suggesting that mismatch repair of overlap HETs could be the source of close triple exchanges. Thus, a significant part, and perhaps all, of the high negative interference for close-marker recombination observed in this system is a direct consequence of the fine structure of the recombinational intermediates. These findings are compatible with recombination models proposed by others, in which a single branched intermediate can give rise to HETs of both the overlap and insertion types.
通过检查内部杂合子(HETs)(重组事件的直接产物)的结构,对噬菌体T5杂交中紧密重组形成的过程进行了研究。选择T5系统是因为它仅允许对内部杂合子进行研究,从而避免了先前对T4研究中固有的模糊性。杂合子是通过对八因子杂交中过早裂解样品中的子代噬菌体进行非选择性筛选获得的。每个HET的分子结构是根据其子代中显示的链基因型推断出来的。这项研究提供了明确的证据,表明重叠和插入HETs都是重组形成的中间体,并且插入HETs是紧密双重组体的重要来源。有证据表明,重叠HETs的错配修复可能是紧密三交换的来源。因此,在该系统中观察到的紧密标记重组的高负干扰的很大一部分,甚至可能全部,是重组中间体精细结构的直接结果。这些发现与其他人提出的重组模型一致,在该模型中,单个分支中间体可以产生重叠和插入类型的HETs。