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噬菌体T4头部DNA包装模型。

Model for DNA packaging into bacteriophage T4 heads.

作者信息

Black L W, Silverman D J

出版信息

J Virol. 1978 Nov;28(2):643-55. doi: 10.1128/JVI.28.2.643-655.1978.

Abstract

The mechanism of DNA packaging into bacteriophage T4 heads in vivo was investigated by glucosylation of hydroxymethylcytosine residues in a conditionally glucose-deficient host. Cytoplasmic DNA associated with partially packaged ts49 heads can be fully glucosylated, whereas DNA already packaged into these heads is shown to be resistant to glucosylation. After temperature shift and completion of arrested packaging into the reversible temperature-sensitive ts49 head, the structure of the DNA in the mature ts49 phage was investigated by restriction enzyme digestion, autoradiography, and other techniques. Such mature DNA appears to be fully glucosylated along part of its length and nonglucosylated on the remainder. Its structure suggests that the DNA is run into the head linearly and unidirectionally from one mature end and that there is little sequence specificity in that portion of the T4 DNA which first enters the capsid. This technique should be useful in investigation of the three-dimensional structure of first- and last-packaged DNA within the head; preliminary studies including autoradiography of osmotically shocked phage suggest that the DNA which first enters the head is deposited toward the center of the capsid and that the end of the DNA which first enters the head exits first upon injection. In conjunction with studies of the structure of condensed DNA, the positions and functions of T4 capsid proteins in DNA packaging, and the order of T4 packaging functions [Earnshaw and Harrison, Nature (London) 268:598-602, 1977; Hsiao and Black, Proc. Natl. Acad. Sci. U.S.A. 74:3652-3656, 1977; Müller-Salamin et al., J. Virol. 24:121-134, 1977; Richards et al., J. Mol. Biol. 78:255-259, 1973], the features described above suggest the following model: the first DNA end is fixed to the proximal apex of the head at p20 and the DNA is then pumped into the head enzymatically by proteins (p20 + p17) which induce torsion in the DNA molecule.

摘要

通过在条件性葡萄糖缺乏的宿主中对羟甲基胞嘧啶残基进行糖基化,研究了噬菌体T4头部DNA在体内的包装机制。与部分包装的ts49头部相关的细胞质DNA可以被完全糖基化,而已经包装到这些头部的DNA则显示对糖基化具有抗性。在温度转换以及将包装停滞在可逆温度敏感的ts49头部完成之后,通过限制性内切酶消化、放射自显影和其他技术研究了成熟ts49噬菌体中DNA的结构。这种成熟的DNA似乎在其长度的一部分上完全被糖基化,而其余部分未被糖基化。其结构表明,DNA从一个成熟末端线性且单向地进入头部,并且在首先进入衣壳的T4 DNA部分中几乎没有序列特异性。该技术对于研究头部内首先包装和最后包装的DNA的三维结构应该是有用的;包括对渗透休克噬菌体的放射自显影在内的初步研究表明,首先进入头部的DNA沉积在衣壳的中心,并且首先进入头部的DNA末端在注射时首先排出。结合对浓缩DNA结构、T4衣壳蛋白在DNA包装中的位置和功能以及T4包装功能顺序的研究[厄恩肖和哈里森,《自然》(伦敦)268:598 - 602,1977;萧和布莱克,《美国国家科学院院刊》74:3652 - 3656,1977;米勒 - 萨拉明等人,《病毒学杂志》24:121 - 134,1977;理查兹等人,《分子生物学杂志》78:255 - 259,1973],上述特征提示了以下模型:第一个DNA末端在p20处固定在头部的近端顶点,然后DNA通过在DNA分子中诱导扭转的蛋白质(p20 + p17)酶促地泵入头部。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fc9/354311/db893c38dc50/jvirol00203-0234-a.jpg

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