Hu W Y, Derbyshire K M
Molecular Genetics Program, Wadsworth Center, New York State Department of Health, Albany, New York, USA.
J Bacteriol. 1998 Jun;180(12):3039-48. doi: 10.1128/JB.180.12.3039-3048.1998.
We have examined the targeting preference of the bacterial insertion element IS903 by determining the sites of insertion of a large number of transposition events into the 55-kb conjugative plasmid pOX38. Despite the large target size, all the insertions were clustered in four small distinct regions associated with conjugal DNA transfer. Within these regions, many different sites were used for insertion; however, there were a few sites that IS903 inserted into more than once. Alignment of the insertion sites showed that there was no consensus sequence within the 9-bp target duplication but that there were preferred sequences located symmetrically on either side of the target. This is consistent with target recognition by a dimer or multimer of transposase, with either sequence-specific or structure-specific interactions on both sides of the target. We show further that when one of these preferred regions was cloned into a second conjugative plasmid, pUB307, it was still a preferred target, implying that all the sequences necessary for target selection are contained within this DNA segment. Also, we observed a very strong preference for insertion in a single orientation in pUB307. We examined the possibility that either DNA replication from the origin of vegetative replication, oriV, or the origin of transfer, oriT, might determine this orientation effect. We find that reversing the direction of vegetative replication had no effect on the orientation of transposon insertions; however, reversing the direction of DNA transfer abolished the orientation effect. This supports the idea that conjugal DNA transfer imparts a polarity on the target that is sensed by the transposon.
我们通过确定大量转座事件在55kb接合质粒pOX38上的插入位点,研究了细菌插入元件IS903的靶向偏好。尽管靶标尺寸很大,但所有插入都聚集在与接合DNA转移相关的四个小的不同区域。在这些区域内,许多不同的位点被用于插入;然而,有一些位点IS903不止一次插入。插入位点的比对表明,在9bp的靶标重复序列内没有共有序列,但在靶标的两侧对称地存在偏好序列。这与转座酶二聚体或多聚体对靶标的识别一致,在靶标的两侧具有序列特异性或结构特异性相互作用。我们进一步表明,当这些偏好区域之一被克隆到第二个接合质粒pUB307中时,它仍然是一个偏好靶标,这意味着靶标选择所需的所有序列都包含在该DNA片段中。此外,我们观察到在pUB307中插入时强烈偏好单一方向。我们研究了来自营养复制起点oriV或转移起点oriT的DNA复制可能决定这种方向效应的可能性。我们发现,逆转营养复制方向对转座子插入方向没有影响;然而,逆转DNA转移方向消除了方向效应。这支持了接合DNA转移在靶标上赋予一种极性的观点,这种极性可被转座子感知。