Au T K, Agrawal Pushpa, Harshey Rasika M
Section of Molecular Genetics and Microbiology and Institute of Cellular and Molecular Biology, University of Texas at Austin, Austin, TX 78712, USA.
J Bacteriol. 2006 Mar;188(5):1829-34. doi: 10.1128/JB.188.5.1829-1834.2006.
DNA transposition is central to the propagation of temperate phage Mu. A long-standing problem in Mu biology has been the mechanism by which the linear genome of an infecting phage, which is linked at both ends to DNA acquired from a previous host, integrates into the new host chromosome. If Mu were to use its well-established cointegrate mechanism for integration (single-strand nicks at Mu ends, joined to a staggered double-strand break in the target), the flanking host sequences would remain linked to Mu; target-primed replication of the linear integrant would subsequently break the chromosome. The absence of evidence for chromosome breaks has led to speculation that infecting Mu might use a cut-and-paste mechanism, whereby Mu DNA is cut away from the flanking sequences prior to integration. In this study we have followed the fate of the flanking DNA during the time course of Mu infection. We have found that these sequences are still attached to Mu upon integration and that they disappear soon after. The data rule out a cut-and-paste mechanism and suggest that infecting Mu integrates to generate simple insertions by a variation of its established cointegrate mechanism in which, instead of a "nick, join, and replicate" pathway, it follows a "nick, join, and process" pathway. The results show similarities with human immunodeficiency virus integration and provide a unifying mechanism for development of Mu along either the lysogenic or lytic pathway.
DNA转座对于温和噬菌体Mu的增殖至关重要。Mu生物学中一个长期存在的问题是,感染性噬菌体的线性基因组(其两端与从前一个宿主获得的DNA相连)整合到新宿主染色体中的机制。如果Mu使用其成熟的共整合机制进行整合(在Mu末端产生单链切口,连接到靶标中的交错双链断裂处),那么侧翼宿主序列将仍然与Mu相连;线性整合体的靶标引发复制随后会破坏染色体。缺乏染色体断裂证据导致人们猜测,感染性Mu可能使用一种剪切粘贴机制,即Mu DNA在整合之前从侧翼序列上被剪切下来。在本研究中,我们追踪了Mu感染过程中侧翼DNA的命运。我们发现,这些序列在整合时仍与Mu相连,并且在整合后不久就消失了。这些数据排除了剪切粘贴机制,并表明感染性Mu通过其成熟的共整合机制的一种变体进行整合以产生简单插入,在这种变体中,它遵循的是“切口、连接和加工”途径,而不是“切口、连接和复制”途径。结果显示出与人类免疫缺陷病毒整合的相似性,并为Mu沿溶原或裂解途径发展提供了一种统一机制。