Lammers P J, Golden J W, Haselkorn R
Cell. 1986 Mar 28;44(6):905-11. doi: 10.1016/0092-8674(86)90013-9.
Vegetative cells of the cyanobacterium Anabaena contain an 11 kb DNA element within the coding region of the nifD gene. This element is excised by site-specific recombination between directly repeated 11 bp sequences at each of its ends during differentiation of nitrogen-fixing cells called heterocysts. Site-specific recombination, leading to the same rejoined nifD gene, was observed during propagation in E. coli of a fragment containing the 11 kb element and flanking sequences. An assay for excision of the element in E. coli was developed, based on mini-Mu-lac transposition into the element. Since the 11 kb element lacks an origin of replication, its excision results in loss of lac and conversion of blue colony-forming cells to white on X-gal plates. Insertion and deletion mutagenesis identified a region of the element needed for excision. Mutations in this region could be complemented by a 6 kb fragment containing an open reading frame that runs counter to those of the nif genes, beginning 240 bp from the recombination site.
蓝藻鱼腥藻的营养细胞在nifD基因的编码区域内含有一个11 kb的DNA元件。在称为异形胞的固氮细胞分化过程中,该元件通过其两端直接重复的11 bp序列之间的位点特异性重组被切除。在含有11 kb元件和侧翼序列的片段于大肠杆菌中繁殖期间,观察到了导致相同重新连接的nifD基因的位点特异性重组。基于mini-Mu-lac转座到该元件中,开发了一种在大肠杆菌中检测该元件切除的方法。由于11 kb元件缺乏复制起点,其切除导致lac缺失,并使在X-gal平板上形成蓝色菌落的细胞转变为白色。插入和缺失诱变确定了切除所需的元件区域。该区域的突变可由一个6 kb的片段互补,该片段包含一个开放阅读框,其方向与nif基因相反,从重组位点开始240 bp。