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单纯疱疹病毒贾斯汀株和F株DNA的BamI、KpnI及SalI限制性酶切图谱:病毒DNA特定区域中异质性的出现情况

BamI, KpnI, and SalI restriction enzyme maps of the DNAs of herpes simplex virus strains Justin and F: occurrence of heterogeneities in defined regions of the viral DNA.

作者信息

Locker H, Frenkel N

出版信息

J Virol. 1979 Nov;32(2):429-41. doi: 10.1128/JVI.32.2.429-441.1979.

Abstract

We present the locations of the cleavage sites for the BamI, KpnI, and SalI restriction endonucleases within the DNA molecules of herpes simplex virus type 1 (HSV-1) strains Justin and F. These restriction enzymes cleave the HSV-1 DNA at many sites, producing relatively small fragments which should prove useful in future studies of HSV-1 gene structure and function. The mapping data revealed the occurrence of heterogeneity within three regions of the viral genome including (i) the region spanning map coordinates 0.74--0.76, (ii) the ends of the large (L) DNA component, and (iii) the junction between the large (L) and the small (S) components. The heterogeneity in the ends of L and the S-L junctions of HSV-1 (Justin) and HSV-1 (F) DNAs was grossly similar to that previously reported to occur in the ends of L and the S-L junctions of the HSV-1 (KOS) DNA (M. J. Wagner and W. C. Summers, J. Virol. 27:374--387, 1978). Thus, cleavage of these regions with restriction endonucleases yielded sets of minor fragments differing in size by constant increments. However, the various strains of HSV-1 differed with respect to the numbers, size increments, and relative molarities of the various minor fragments, suggesting that the parameters of the heterogeneity are inherited in the structural makeup of the HSV-1 genome. The strain dependence of the pattern of heterogeneity can be most easily explained in terms of variable sizes of the terminally reiterated a sequence, contained in the DNA molecules of these three strains of HSV-1.

摘要

我们展示了1型单纯疱疹病毒(HSV-1)毒株贾斯汀(Justin)和F的DNA分子中BamI、KpnI和SalI限制性内切酶的切割位点位置。这些限制性酶在许多位点切割HSV-1 DNA,产生相对较小的片段,这在未来HSV-1基因结构与功能的研究中应会证明是有用的。图谱数据揭示了病毒基因组三个区域内存在异质性,包括:(i)跨度为图谱坐标0.74 - 0.76的区域;(ii)大(L)DNA组分的末端;(iii)大(L)和小(S)组分之间的连接处。HSV-1(贾斯汀)和HSV-1(F)DNA的L末端和S-L连接处的异质性与先前报道的HSV-1(KOS)DNA的L末端和S-L连接处的异质性大致相似(M. J. 瓦格纳和W. C. 萨默斯,《病毒学杂志》27:374 - 387,1978年)。因此,用限制性内切酶切割这些区域产生了一系列大小以恒定增量不同的小片段。然而,HSV-1的各种毒株在各种小片段的数量、大小增量和相对摩尔数方面存在差异,这表明异质性参数是由HSV-1基因组的结构组成所遗传的。异质性模式的毒株依赖性最容易用这三种HSV-1毒株的DNA分子中末端重复a序列的可变大小来解释。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6139/353574/d2c8a30b03ca/jvirol00191-0083-a.jpg

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