Honigberg S M, Rao B J, Radding C M
Proc Natl Acad Sci U S A. 1986 Dec;83(24):9586-90. doi: 10.1073/pnas.83.24.9586.
RecA nucleoprotein filaments found homologous targets even when the latter was mixed with 200,000 times as much heterologous duplex DNA. By contrast, mixing of the single-stranded probe with only 100 times as much heterologous single strands markedly reduced the rate of finding homologous duplex molecules. Titration of the reaction with different proportions of homologous single-stranded DNA distinguished a condition under which the search for homology itself was rate limiting from a condition under which some later step was limiting. Less than 1 min was required to scan 6.4 kilobase pairs of duplex DNA for homology to a RecA-coated single strand of the same size, but these experiments revealed that rapid searching by RecA nucleoprotein filaments was largely confined to neighboring duplex molecules. These observations provide guidelines for the use of RecA protein in locating rare sequences in complex mixtures of duplex DNA, and we describe a simple protocol by which rare sequences can be rapidly enriched at least a thousandfold.
RecA核蛋白丝即使在同源靶标与多达200,000倍的异源双链DNA混合时也能找到同源靶标。相比之下,单链探针与仅100倍量的异源单链混合会显著降低找到同源双链分子的速率。用不同比例的同源单链DNA对反应进行滴定,区分了同源性搜索本身是限速步骤的情况和后续某个步骤是限速步骤的情况。扫描6.4千碱基对的双链DNA以寻找与相同大小的RecA包被单链的同源性只需不到1分钟,但这些实验表明,RecA核蛋白丝的快速搜索主要局限于相邻的双链分子。这些观察结果为在双链DNA复杂混合物中定位稀有序列时使用RecA蛋白提供了指导,并且我们描述了一种简单的方案,通过该方案稀有序列可以快速富集至少一千倍。