Hoess R H, Abremski K
Proc Natl Acad Sci U S A. 1984 Feb;81(4):1026-9. doi: 10.1073/pnas.81.4.1026.
The interaction between the P1 recombinase protein Cre and the DNA site at which it acts, loxP, has been studied by using nuclease protection techniques. The region of DNA protected by Cre against nuclease attack by DNase I or neocarzinostatin is a 34-base-pair (bp) region containing two 13-bp inverted repeats separated by an 8-bp spacer region. These protected sequences have previously been shown to be required for efficient Cre-mediated recombination at loxP. The results of the above protection experiments suggest (i) that no more than 34 bp may be required for loxP recombination and (ii) that the asymmetry of loxP recombination is due to the 8-bp spacer sequence. With neocarzinostatin, a specific nucleotide within the 8-bp spacer region is not protected. This nucleotide is located in a 2-bp sequence shown to be involved in a loxP crossover event, suggesting that this region remains exposed after Cre binding. Protection experiments have also been done with loxP sites that have either the left or right inverted repeat deleted. The nuclease protection pattern of these sites reveals that each loxP site consists of two binding domains for Cre, each being composed of one 13-bp inverted repeat and the contiguous 4 bp of the 8-bp spacer region.
通过核酸酶保护技术研究了P1重组酶蛋白Cre与其作用的DNA位点loxP之间的相互作用。Cre保护免受DNA酶I或新制癌菌素核酸酶攻击的DNA区域是一个34碱基对(bp)的区域,包含两个由8 bp间隔区隔开的13 bp反向重复序列。这些受保护的序列先前已被证明是loxP处高效Cre介导的重组所必需的。上述保护实验的结果表明:(i)loxP重组可能只需要不超过34 bp;(ii)loxP重组的不对称性是由于8 bp间隔序列所致。对于新制癌菌素,8 bp间隔区内的一个特定核苷酸未受到保护。该核苷酸位于一个2 bp序列中,该序列已被证明参与loxP交叉事件,这表明该区域在Cre结合后仍保持暴露状态。还对缺失了左或右反向重复序列的loxP位点进行了保护实验。这些位点的核酸酶保护模式表明,每个loxP位点由两个Cre结合结构域组成,每个结构域由一个13 bp反向重复序列和8 bp间隔区中相邻的4 bp组成。