Ramaswamy K S, Carrasco C D, Fatma T, Golden J W
Department of Biology, Texas A&M University, College Station 77843-3258, USA.
Mol Microbiol. 1997 Mar;23(6):1241-9. doi: 10.1046/j.1365-2958.1997.3081671.x.
The fdxN element, along with two other DNA elements, is excised from the chromosome during heterocyst differentiation in Anabaena sp. strain PCC 7120. Previous work showed that rearrangement of the fdxN element requires the xisF gene, which encodes a site-specific recombinase, and suggested that at least one other heterocyst-specific factor is involved. Here we report that the xisH and xisI genes are necessary for the heterocyst-specific excision of the fdxN element. Deletion of a 3.2 kb region downstream of the xisF gene blocked the fdxN-element rearrangement in heterocysts. The 3.2 kb deletion was complemented by the two overlapping genes xisH and xisI. Interestingly, extra copies of xisHI on a replicating plasmid resulted in the xisF-dependent excision of the fdxN element in vegetative cells. Therefore, xisHI are involved in the control of cell-type specificity of the fdxN rearrangement. The xisHI genes had no effect on the two other DNA rearrangements. The xisHI-induced excision of the fdxN element produced strains lacking the element and demonstrates that the 55 kb element contains no essential genes. xisH and xisI do not show similarity to any known genes.
在鱼腥藻PCC 7120菌株异形胞分化过程中,fdxN元件与另外两个DNA元件一起从染色体上切除。先前的研究表明,fdxN元件的重排需要xisF基因,该基因编码一种位点特异性重组酶,并表明至少还涉及一种其他异形胞特异性因子。在此,我们报告xisH和xisI基因对于fdxN元件的异形胞特异性切除是必需的。xisF基因下游3.2 kb区域的缺失阻断了异形胞中fdxN元件的重排。3.2 kb的缺失由两个重叠基因xisH和xisI互补。有趣的是,复制质粒上xisHI的额外拷贝导致营养细胞中fdxN元件的xisF依赖性切除。因此,xisHI参与了fdxN重排的细胞类型特异性控制。xisHI基因对其他两种DNA重排没有影响。xisHI诱导的fdxN元件切除产生了缺乏该元件的菌株,并证明55 kb的元件不包含必需基因。xisH和xisI与任何已知基因均无相似性。