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在赛氏疱疹病毒转化的淋巴样细胞系中的游离病毒DNA。

Episomal viral DNA in a Herpesvirus saimiri-transformed lymphoid cell line.

作者信息

Werner F J, Bornkamm G W, Fleckenstein B

出版信息

J Virol. 1977 Jun;22(3):794-803. doi: 10.1128/JVI.22.3.794-803.1977.

Abstract

The lymphoid cell line #1670 has been derived from the infiltrated spleen of a tumor-bearing marmoset monkey infected with Herpesvirus saimiri. The cells contain both types of H. saimiri DNA, unique light (L-) DNA (36% cytosine plus guanine) and repetitive heavy (H-) DNA (71% cytosine plus guanine), without producing infectious virus. Viral DNA was found to persist in these cells as nonintegrated circular DNA molecules. Closed circular superhelical viral DNA molecules were isolated by three subsequent centrifugation steps: (i) isopycnic centrifugation in CsCl, (ii) sedimentation through glycerol gradients, and (iii) equilibrium centrifugation in CsCl-ethidium bromide. The isolated circles had a molecular weight of 131.5 +/- 3.6 x 10(6). This is significantly higher than the molecular weight of linear DNA molecules isolated from purified H. saimiri virions (about 100 x 10(6)). Partial denaturation mapping of circular molecules from #1670 lymphoid cells showed uniform arrangement of H- and L-DNA sequences in all circles. All denatured molecules contained two L-DNA regions (molecular weights of 54.0 +/- 1.8 x 10(6) and 31.5 +/- 1.3 x 10(6)) and two H-DNA regions (molecular weight of 25.6 +/- 1.9 x 10(6) and 20.0 +/- 0.8 x 10(6)) of constant length. Maps of both L-regions suggested that the sequences of the shorter L-DNA region were a subset of those of the longer region. The sequences of both L-regions had the same orientation. Circular molecules from H. saimiri-transformed lymphoid cell line #1670 appeared to represent defective genomes, containing only 75% of the genetic information present in L-DNA of H. saimiri virions.

摘要

淋巴样细胞系#1670源自感染了赛米里疱疹病毒的荷瘤狨猴的浸润脾脏。这些细胞含有两种类型的赛米里疱疹病毒DNA,即独特的轻(L-)DNA(胞嘧啶加鸟嘌呤含量为36%)和重复重(H-)DNA(胞嘧啶加鸟嘌呤含量为71%),但不产生感染性病毒。发现病毒DNA以非整合的环状DNA分子形式在这些细胞中持续存在。通过随后的三个离心步骤分离出闭环超螺旋病毒DNA分子:(i)在CsCl中进行等密度离心,(ii)通过甘油梯度沉降,以及(iii)在CsCl-溴化乙锭中进行平衡离心。分离出的环状分子的分子量为131.5±3.6×10⁶。这明显高于从纯化的赛米里疱疹病毒颗粒中分离出的线性DNA分子的分子量(约100×10⁶)。对#1670淋巴样细胞的环状分子进行的部分变性图谱分析表明,所有环状分子中H-和L-DNA序列排列均匀。所有变性分子都含有两个长度恒定的L-DNA区域(分子量分别为54.0±1.8×10⁶和31.5±1.3×10⁶)和两个H-DNA区域(分子量分别为25.6±1.9×10⁶和20.0±0.8×10⁶)。两个L区域的图谱表明,较短L-DNA区域的序列是较长区域序列的一个子集。两个L区域的序列具有相同的方向。来自赛米里疱疹病毒转化的淋巴样细胞系#1670的环状分子似乎代表有缺陷的基因组,仅包含赛米里疱疹病毒颗粒L-DNA中75%的遗传信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3be3/515778/aace57a50232/jvirol00210-0225-a.jpg

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