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Molecular genetics of herpes simplex virus: Demonstration of regions of obligatory and nonobligatory identity within diploid regions of the genome by sequence replacement and insertion

机译:单纯疱疹病毒的分子遗传学:通过序列替换和插入来证明基因组二倍体区域内强制性和非强制性同一性的区域

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摘要

The DNAs of herpes simplex virus (HSV) 1 and 2 consist of two components, L and S, each composed of unique sequences bracketed by inverted repeats. In this study we have probed the structure of the reiterated regions of the S component in marker rescue experiments involving transfection of cells with mixtures of intact HSV-1 mutant viral DNA and individual DNA fragments generated by restriction endonuclease digestion of wild-type HSV-1 or HSV-2 DNAs. The results were as follows: (i) HSV is diploid for the wild-type sequences that rescue two temperature-sensitive (ts) mutants. DNA fragments from both reiterated regions of the S component of HSV-1(F) DNA can rescue tsLB2 and tsD mutants. (ii) Identity of the entire reiterated sequence at both ends of S is not obligatory because only one end of the S component of wild phenotype virus HSV-1(1061) rescues tsD even though both ends rescue tsLB2. (iii) Genes in both reiterated sequences can be expressed. We produced, by marker rescue experiments, recombinants with heterotypic ends of the S component, and these specified corresponding polypeptides characteristic of both HSV-1 and HSV-2. (iv) The reiterated sequences of the S component may contain a region of obligatory identity. Thus, several recombinant clones produced by rescue with HSV-2 DNA contained identical HSV-2 DNA insertions within both reiterated regions of the HSV-1 S component. Consistent with this conclusion, the termini of the S component in the heterodiploids described in iii were identical by restriction enzyme analysis. (v) The observation that HSV DNA can be expanded by at least 5 × 106 by means of insertion in the S component suggests that it can be a vehicle for exogenous DNA.
机译:单纯疱疹病毒(HSV)1和2的DNA由两个部分组成,即L和S,每个部分都由被反向重复括起来的独特序列组成。在这项研究中,我们已经在标记物拯救实验中探究了S成分重复区域的结构,该实验涉及用完整HSV-1突变病毒DNA和限制性核酸内切酶消化野生型HSV-1产生的单个DNA混合物转染细胞或HSV-2 DNA。结果如下:(i)HSV是拯救两个温度敏感(ts)突变体的野生型序列的二倍体。 HSV-1(F)DNA S成分的两个重复区域的DNA片段可以拯救tsLB2和tsD突变体。 (ii)在S两端不需要完全重复序列的同一性,因为野生表型病毒HSV-1(1061)的S成分只有一个末端可以拯救tsD,即使两个末端都可以拯救tsLB2。 (iii)两个重复序列中的基因都可以表达。我们通过标志物挽救实验,产生了具有S成分异型末端的重组体,以及这些具有HSV-1和HSV-2特异特征的多肽。 (iv)S成分的重复序列可以包含一个强制同一性区域。因此,通过用HSV-2 DNA抢救产生的几个重组克隆在HSV-1S组分的两个重复区域内包含相同的HSV-2 DNA插入。与该结论一致,通过限制酶分析,iii中所述的异二倍体中的S成分的末端相同。 (v)观察到,通过插入S组分,HSV DNA可以扩增至少5×10 6 ,这表明它可以作为外源DNA的载体。

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