Pearson R K, Fox M S
Department of Biology, Massachusetts Institute of Technology, Cambridge, 02139, USA.
Genetics. 1988 Jan;118(1):5-12. doi: 10.1093/genetics/118.1.5.
We have examined the impact of DNA heterologies on the packaging of lambda DNA in vitro. Heterology-containing DNA molecules were constructed by denaturing and reannealing a mixture of DNA from cI+ phage and DNA front phage carrying small insertion or deletion mutations in the cI gene. We found that molecules with heterologies of up to 19 base pairs (bp) can be packaged as viable heterozygous phage with approximately the same efficiency as molecules with a base pair mismatch. In contrast, with a heterology of 26-bp heterozygous plaque formers are rare. In principle, the absence of cI heterozygotes among packaged phage may be due either to a failure to encapsulate the DNA or a failure to inject the packaged DNA on infection. Southern blot analysis of DNA isolated from packaged phage indicates that DNA harboring a 26-bp heterology is almost completely absent in packaged phage. Thus, an upper limit has been established for the size of heterology that can be accommodated by the packaging apparatus The size of the connector portal could be the basis for this limit.
我们已经研究了DNA异源性对λ噬菌体DNA体外包装的影响。通过使来自cI⁺噬菌体的DNA与携带cI基因小插入或缺失突变的噬菌体DNA混合物变性并重新退火,构建了含有异源序列的DNA分子。我们发现,具有高达19个碱基对(bp)异源序列的分子可以作为有活力的杂合噬菌体进行包装,其效率与具有一个碱基对错配的分子大致相同。相比之下,具有26-bp异源序列的杂合噬菌斑形成体很少见。原则上,包装的噬菌体中不存在cI杂合子可能是由于未能封装DNA,或者是在感染时未能注入包装好的DNA。对从包装的噬菌体中分离的DNA进行Southern印迹分析表明,携带26-bp异源序列的DNA在包装的噬菌体中几乎完全不存在。因此,已经确定了包装装置能够容纳的异源序列大小的上限。连接门户的大小可能是这个限制的基础。