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Physical and Genetic Characterization of Deletion Mutants of Simian Virus 40 Constructed In Vitro

机译:体外构建的猿猴病毒40缺失突变体的物理和遗传特性

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摘要

Mutants of simian virus 40 (SV40), with deletions ranging in size from fewer than 3 to 750 base pairs located throughout the SV40 genome, were obtained by infecting CV-1P cells with linear SV40 DNA and DNA of an appropriate helper virus. The linear DNA was obtained by complete cleavage of closed circular DNA with Hae II or Bam HI endonuclease or partial cleavage with either Hae III endonuclease or nuclease S1, followed, in some cases, by mild digestion with phage λ 5′ -exonuclease. The following mutants with deletions in the late region of the SV40 genome were obtained and characterized. Ten, containing deletions at the Hae II endonuclease site (map location 0.83), define a new genetic complementation group, E, grow extremely slowly without helper virus, and cause alterations only in VP2. Two mutants with deletions in the region 0.92 to 0.945 affect both VP2 and VP3, demonstrating that VP3 shares sequences with the C-terminal portion of VP2. The mutant with a deletion at 0.93 is the first deletion mutant in the D complementation group and is also temperature sensitive; the mutant with a deletion at 0.94 is viable and grows normally. Three mutants with deletions at the EcoRI endonuclease site (0/1.0) and eleven with deletions at the BamHI endonuclease site (0.15) fall into the B/C complementation group. Six additional mutants with deletions at the BamHI endonuclease site are viable, growing more slowly than wild type. VP1 is the only polypeptide affected by mutants in the B/C group. A mutant with a deletion of the region 0.72 to 0.80 has a polar effect, failing to express the E, D, and B/C genes. Mutants with deletions in the early region (0.67 counterclockwise to 0.17) at 0.66 to 0.59, 0.48, 0.47, 0.33, and 0.285 to 0.205 are all members of the A complementation group. Thus, the A gene is the only viral gene in the early region whose expression is necessary for productive infection of permissive cells. Since mutants with deletions in the region 0.59 to 0.54 are viable, two separate regions are essential for expression of the gene A function: 0.66 to 0.59 and 0.54 to 0.21. Mutants with deletions at 0.21 and 0.18 are viable. Approximate map locations of SV40 genes and possible models for their regulation are discussed.
机译:通过用线性SV40 DNA和合适的辅助病毒DNA感染CV-1P细胞,获得猿猴病毒40(SV40)突变体,其缺失范围在整个SV40基因组中少于3至750个碱基对。通过用Hae II或Bam HI核酸内切酶完全切割封闭的环状DNA或通过Hae III内切核酸酶或核酸酶S1进行部分切割,然后在某些情况下用噬菌体λ5'-核酸外切酶温和消化,获得线性DNA。获得并表征了以下在SV40基因组的晚期区域具有缺失的突变体。十个在Hae II核酸内切酶位点(图位置0.83)包含缺失,定义了一个新的遗传互补基团E,在没有辅助病毒的情况下生长极其缓慢,仅在VP2中引起改变。两个在0.92至0.945区域有缺失的突变体同时影响VP2和VP3,这表明VP3与VP2的C端部分共享序列。在0.93处缺失的突变体是D互补组中的第一个缺失突变体,并且也是温度敏感的。缺失0.94的突变体是有活力的,并且可以正常生长。在EcoRI核酸内切酶位点(0 / 1.0)处缺失的三个突变体和在BamHI核酸内切酶位点处(0.15)缺失的11个突变体属于B / C互补组。 BamHI核酸内切酶位点缺失的另外六个突变体是可行的,其生长速度比野生型慢。 VP1是唯一受B / C组突变体影响的多肽。缺失0.72至0.80区域的突变体具有极性效应,无法表达E,D和B / C基因。在早期区域(逆时针为0.67至0.17)缺失的突变体在0.66至0.59、0.48、0.47、0.33和0.285至0.205都是A互补组的成员。因此,A基因是早期区域中唯一的病毒基因,其表达对于允许性细胞的有效感染是必需的。由于具有在0.59至0.54区域中缺失的突变体是可行的,因此两个单独的区域对于基因A功能的表达是必不可少的:0.66至0.59和0.54至0.21。在0.21和0.18处缺失的突变体是可行的。讨论了SV40基因的大概图谱位置及其调控模型。

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