Cassier-Chauvat C, Poncelet M, Chauvat F
Service de Biochimie et Génétique Moléculaire, CEA Saclay, URA 2096 CNRS, Gif sur Yvette, France.
Gene. 1997 Aug 22;195(2):257-66. doi: 10.1016/s0378-1119(97)00165-0.
Three insertion sequences were characterized from the widely-used cyanobacterium Synechocystis PCC6803. They all harbored a putative transposase sequence flanked by two imperfect inverted repeats, seemed to have duplicated their target insertion site and occurred as multiple copies in the host genome. They exhibited no obvious homology with any other cyanobacterial ISs and were termed IS5S (871 bp), IS4S (1299 bp) and ISS1987 (949 bp) because they were, respectively, homologous to IS5- and IS4-bacterial elements, and to several members of the IS630-Tc1-mariner superfamily of IS elements occurring in a wide range of hosts. This suggests that these IS-elements were spread through horizontal transfer between evolutionary distant organisms. Three IS5S-copies were isolated as a rescue insertion into a replicating plasmid (IS5Sa), or subsequently cloned from a Synechocystis DNA-library probed with IS5Sa (IS5Sb and IS5Sc), and appeared to be almost identical. In the vicinity of IS5Sb, we found the ISS1987 element inserted into the IS4S element. This indicates that the ISS1987 element has been, and could still be, mobile since its transposase sequence is not interrupted with stop codons or translational frameshifts, unlike that which is found in most members of the IS630-Tc1-mariner superfamily of transposable elements.
从广泛使用的蓝藻集胞藻PCC6803中鉴定出三个插入序列。它们都含有一个推测的转座酶序列,两侧是两个不完全的反向重复序列,似乎复制了其靶插入位点,并以多个拷贝的形式存在于宿主基因组中。它们与任何其他蓝藻插入序列均无明显同源性,分别被命名为IS5S(871 bp)、IS4S(1299 bp)和ISS1987(949 bp),因为它们分别与IS5和IS4细菌元件同源,以及与广泛宿主中出现的IS630-Tc1-mariner插入序列超家族的几个成员同源。这表明这些插入序列元件是通过水平转移在进化距离较远的生物体之间传播的。三个IS5S拷贝被分离出来,一个作为拯救插入到复制质粒中(IS5Sa),或者随后从用IS5Sa探针筛选的集胞藻DNA文库中克隆出来(IS5Sb和IS5Sc),它们看起来几乎相同。在IS5Sb附近,我们发现ISS1987元件插入到了IS4S元件中。这表明ISS1987元件一直以来并且可能仍然具有移动性,因为其转座酶序列不像大多数IS630-Tc1-mariner转座元件超家族成员那样被终止密码子或翻译移码打断。