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首页> 外文期刊>Virus Genes >Cloning of E6 and E7 genes of human papilloma virus type 18 and transformation potential of E7 gene and its mutants.
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Cloning of E6 and E7 genes of human papilloma virus type 18 and transformation potential of E7 gene and its mutants.

机译:人乳头瘤病毒18型E6和E7基因的克隆及其E7基因及其突变体的转化潜力。

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E6 and E7 genes of human papilloma virus type 18 have been subcloned from plasmid pC7, carrying an insert of DNA from squamous cell carcinoma of cervix. Both genes in comparison to prototype variant contain one mutation that changes asparagine to leucine. In the case of E6 gene this mutation is mapped in codon 129, in the case of E7 the same change AAC to AAA mapped in codon 92. In addition both genes contain few point mutations that do not change the aminoacid sequences of the protein. Two mutants of E7 gene have been constructed by site directed mutagenesis based on PCR technology-one in codon 10 (change Asp to Asn) and one in codon 24 (change Asp to Gly). The first type of mutation did not influence the transformation potential of the E7 gene in comparison to the parental one with mutation in codon 92. The mutation in codon 24 (region responsible for the interaction with Rb protein) eliminate the transformation potential of the gene. The cells transformed with E7 mutants in codons 10 and 92 were tumorigenic for syngenic rats.
机译:人乳头瘤病毒18型的E6和E7基因已从质粒pC7中亚克隆,该质粒带有子宫颈鳞状细胞癌的DNA插入片段。与原型变体相比,这两个基因均包含一个突变,该突变将天冬酰胺变为亮氨酸。在E6基因的情况下,该突变被定位在129号密码子中,在E7基因的情况下,相同的AAC变成了在92号密码子中所映射的AAA。此外,两个基因都包含很少的不改变蛋白质氨基酸序列的点突变。通过基于PCR技术的定点诱变已经构建了E7基因的两个突变体,一个在密码子10中(将Asp变为Ast),一个在密码子24中(将Asp变为Gly)。与具有密码子92突变的亲本相比,第一类突变不影响E7基因的转化潜能。密码子24(负责与Rb蛋白相互作用的区域)中的突变消除了该基因的转化潜能。用E7突变体在密码子10和92中转化的细胞对同系大鼠具有致瘤性。

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