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一种用于噬菌体T4包装长度小于满头部长度DNA分子的不连续满头部包装模型。

A discontinuous headful packaging model for packaging less than headful length DNA molecules by bacteriophage T4.

作者信息

Leffers G, Rao V B

机构信息

Department of Biology, Catholic University of America, Washington, DC 20064, USA.

出版信息

J Mol Biol. 1996 May 24;258(5):839-50. doi: 10.1006/jmbi.1996.0291.

Abstract

Bacteriophage T4 and other double-stranded DNA-containing bacteriophages package DNA by the classical headful packaging mechanism. In this mechanism, the packaging machinery cuts a DNA concatemer and packages a single unit length genome within the viral capsid. The length of the packaged DNA molecule is determined by the size of the viral capsid. Surprisingly, during large DNA cloning experiments, we observed that the in vitro phage T4 packaging system can package and transduce DNA molecules that are much smaller than the T4 headful size. We analyzed this phenomenon by using defined plasmid DNAs as substrates for in vitro packaging. The data showed that phage T4 can successfully package and transduce 4 to 29 kb plasmid DNA molecules. When two plasmid DNAs with different antibiotic markers were added to the packaging reaction mixture, transductants that are resistant to both the antibiotics were obtained, suggesting that both the plasmid DNAs are packaged within the same head. Analysis of the transducing particles by equilibrium CsCl density-gradient centrifugation showed that the particles have the same density as the wild-type phage. That the less than headful length molecules were not converted to T4 headful length prior to packaging was established by a number of independent approaches. Finally, unit length plasmid DNA molecules of appropriate size were isolated from the in vitro packaged particles. Based on these data, we propose a discontinuous headful packaging model for packaging less than headful length molecules. In this model, the packaging machinery packages the first available less than headful length DNA molecule and generates a partially full head. The partially full head then reinitiates packaging on a second DNA molecule. This process continues until the head is filled with DNA.

摘要

噬菌体T4和其他含双链DNA的噬菌体通过经典的满头部包装机制来包装DNA。在这种机制中,包装机制切割DNA多联体,并将单个单位长度的基因组包装在病毒衣壳内。包装的DNA分子的长度由病毒衣壳的大小决定。令人惊讶的是,在大型DNA克隆实验中,我们观察到体外噬菌体T4包装系统能够包装和转导比T4满头部大小小得多的DNA分子。我们通过使用确定的质粒DNA作为体外包装的底物来分析这种现象。数据表明,噬菌体T4能够成功地包装和转导4至29 kb的质粒DNA分子。当将两个带有不同抗生素标记的质粒DNA添加到包装反应混合物中时,获得了对两种抗生素都有抗性的转导子,这表明两种质粒DNA都被包装在同一个头部内。通过平衡CsCl密度梯度离心对转导颗粒进行分析表明,这些颗粒与野生型噬菌体具有相同的密度。通过多种独立方法确定,小于满头部长度的分子在包装之前并未转化为T4满头部长度。最后,从体外包装的颗粒中分离出适当大小的单位长度质粒DNA分子。基于这些数据,我们提出了一种用于包装小于满头部长度分子的不连续满头部包装模型。在这个模型中,包装机制包装第一个可用的小于满头部长度的DNA分子,并产生一个部分充满的头部。然后,这个部分充满的头部在第二个DNA分子上重新启动包装。这个过程持续进行,直到头部充满DNA。

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