Buerstedde Jean-Marie, Lowndes Noel, Schatz David G
Centre for Chromosome Biology, School of Natural Sciences, National University of Ireland, Galway, Galway, Ireland
Centre for Chromosome Biology, School of Natural Sciences, National University of Ireland, Galway, Galway, Ireland.
Elife. 2014 Jul 8;3:e03110. doi: 10.7554/eLife.03110.
The activation induced cytidine deaminase (AID) protein is known to initiate somatic hypermutation, gene conversion or switch recombination by cytidine deamination within the immunoglobulin loci. Using chromosomally integrated fluorescence reporter transgenes, we demonstrate a new recombinogenic activity of AID leading to intra- and intergenic deletions via homologous recombination of sequence repeats. Repeat recombination occurs at high frequencies even when the homologous sequences are hundreds of bases away from the positions of AID-mediated cytidine deamination, suggesting DNA end resection before strand invasion. Analysis of recombinants between homeologous repeats yielded evidence for heteroduplex formation and preferential migration of the Holliday junctions to the boundaries of sequence homology. These findings broaden the target and off-target mutagenic potential of AID and establish a novel system to study induced homologous recombination in vertebrate cells.DOI: http://dx.doi.org/10.7554/eLife.03110.001.
已知激活诱导胞苷脱氨酶(AID)蛋白通过免疫球蛋白基因座内的胞苷脱氨作用引发体细胞超突变、基因转换或类别转换重组。利用染色体整合的荧光报告转基因,我们证明了AID的一种新的重组活性,即通过序列重复的同源重组导致基因内和基因间缺失。即使同源序列距离AID介导的胞苷脱氨位置有数百个碱基之遥,重复重组仍以高频发生,这表明在链侵入之前发生了DNA末端切除。对同源重复序列之间重组体的分析为异源双链体形成以及霍利迪连接点向序列同源性边界的优先迁移提供了证据. 这些发现拓宽了AID的靶向和脱靶诱变潜力,并建立了一个研究脊椎动物细胞中诱导同源重组的新系统。DOI: http://dx.doi.org/10.7554/eLife.03110.001。