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首页> 外文期刊>Journal of Molecular Biology >HEADFUL PACKAGING REVISITED - THE PACKAGING OF MORE THAN ONE DNA MOLECULE INTO A BACTERIOPHAGE P1 HEAD
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HEADFUL PACKAGING REVISITED - THE PACKAGING OF MORE THAN ONE DNA MOLECULE INTO A BACTERIOPHAGE P1 HEAD

机译:改头换面-将多于一种DNA分子包装入噬菌体P1头中

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摘要

Like a variety of other bacteriophages, such as T4 and P22, bacteriophage P1 packages DNA by a ''headful'' mechanism in which the capacity of the viral capsid determines the size of the single DNA molecule that is packaged. Because of the long-standing and general acceptance of this packaging mechanism, we were surprised to discover that some of our observations, using the in vitro P1 packaging system, could be explained by the packaging of less than headful-sized (<110 kb) DNA molecules into a PI capsid. To account for these observations, we describe results that support a model of in vitro P1 packaging in which multiple less than headful-sized DNA molecules are taken into a P1 head until that head has been filled. The results further suggest that the phage so generated can occasionally inject more than one DNA molecule into a cell upon viral infection. The data that supports these conclusions are: (1) the DNAs of the circular P1 cloning vectors pAd10sacBII (32 kb) and pNS358 (14 kb) are packaged in vitro with an efficiency of about 6 to 12 % of that of longer concatemers of these DNAs. (2) The in vitro packaging of two differentially marked, less than 18 kb plasmid DNAs in the same reaction results in the production of a phage that can occasionally inject both DNAs into the same cell upon infection. (3) Virus particles generated by the packaging of either pAd10sacBII plasmid DNA or the two differently marked plasmids have a density in CsCl equilibrium gradients that is the same as P1 plaque-forming phage, suggesting that the former phage contain a headful of DNA. These results cannot be explained by Cre-mediated site-specific recombination between plasmids in the P1 packaging extracts. Finally we present in vivo experiments that are also consistent with the headful packaging of multiple DNAs into a P1 head. [References: 20]
机译:与T4和P22等其他各种噬菌体一样,噬菌体P1通过“头部”机制包装DNA,其中病毒衣壳的能力决定了被包装的单个DNA分子的大小。由于这种封装机制已长期存在并被普遍接受,我们惊讶地发现,使用体外P1封装系统的某些观察结果可以用小于头部(小于110 kb)的封装来解释DNA分子变成PI衣壳。为了解释这些观察结果,我们描述了支持体外P1包装模型的结果,在该模型中,将少于头个大小的多个DNA分子放入P1头中,直到该头被装满为止。结果进一步表明,如此产生的噬菌体在病毒感染后偶尔可将一个以上的DNA分子注入细胞。支持这些结论的数据是:(1)环形包装的P1克隆载体pAd10sacBII(32 kb)和pNS358(14 kb)的DNA在体外包装,其效率约为这些较长的串联体的6%至12% DNA。 (2)在同一反应中体外包装两个差异标记的,少于18 kb的质粒DNA导致噬菌体的产生,该噬菌体在感染后有时可将两个DNA注入同一细胞。 (3)通过包装pAd10sacBII质粒DNA或两个不同标记的质粒产生的病毒颗粒在CsCl平衡梯度中的密度与形成P1噬菌斑的噬菌体相同,这表明前一个噬菌体含有大量DNA。这些结果不能通过Cre介导的P1包装提取物中质粒之间的位点特异性重组来解释。最后,我们提出了体内实验,这些实验也与将多个DNA的有效包装包装成P1头相一致。 [参考:20]

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