首页> 美国卫生研究院文献>Nucleic Acids Research >Mutagenicity of a unique thymine-thymine dimer or thymine-thymine pyrimidine pyrimidone (6-4) photoproduct in mammalian cells.
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Mutagenicity of a unique thymine-thymine dimer or thymine-thymine pyrimidine pyrimidone (6-4) photoproduct in mammalian cells.

机译:独特的胸腺嘧啶-胸腺嘧啶二聚体或胸腺嘧啶-胸腺嘧啶嘧啶嘧啶酮(6-4)光产物在哺乳动物细胞中的致突变性。

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摘要

The mutagenic properties of UV-induced photoproducts, both the cis-syn thymine-thymine dimer (TT) and the thymine-thymine pyrimidine pyrimidone (6-4) photoproduct [T(6-4)T] were studied in mammalian cells using shuttle vectors. A shuttle vector able to replicate in both mammalian cells and bacteria was produced in its single-stranded DNA form. A unique photoproduct was inserted at a single restriction site and after recircularization of the single-stranded DNA vector, this latter was transfected into simian COS7 cells. After DNA replication the vector was extracted from cells and used to transform bacteria. Amplified DNA was finally analyzed without any selective screening, DNA from randomly picked bacterial colonies being directly sequenced. Our results show clearly that both lesions are mutagenic, but at different levels. Mutation frequencies of 2 and 60% respectively were observed with the TT dimer and the T(6-4)T. With the TT dimer the mutations were targeted on the 3'-T. With the T(6-4)T a large variety of mutations were observed. A majority of G-->T transversions were semi-targeted to the base before the 5'-T of the photoproduct. These kinds of mutations were not observed when the same plasmid was transfected directly into SOS-induced JM105 bacteria or when the T(6-4)T oligonucleotide inserted in a different plasmid was replicated in SOS-induced SMH10 Escherichia coil bacteria. These semi-targeted mutations are therefore the specific result of bypass of the T(6-4)T lesion in COS7 cells by one of the eukaryotic DNA polymerases.
机译:使用穿梭在哺乳动物细胞中研究了紫外线诱导的光产物(顺式-胸腺嘧啶-胸腺嘧啶二聚体(TT)和胸腺嘧啶-胸腺嘧啶嘧啶嘧啶酮(6-4)光产物[T(6-4)T])的诱变特性。向量。能够在哺乳动物细胞和细菌中复制的穿梭载体以其单链DNA形式产生。将独特的光产物插入单个限制性酶切位点,并将单链DNA载体重新环化后,将其转染到猿猴COS7细胞中。 DNA复制后,从细胞中提取载体并用于转化细菌。最后,无需任何选择性筛选就可以分析扩增后的DNA,直接对随机挑选的细菌菌落中的DNA进行测序。我们的结果清楚地表明,两种病变都是致突变性的,但水平不同。 TT二聚体和T(6-4)T的突变频率分别为2%和60%。使用TT二聚体,突变靶向3'-T。使用T(6-4)T可以观察到各种各样的突变。大多数G-> T转换都在光产物的5'-T之前半靶向到碱基。当相同的质粒直接转染到SOS诱导的JM105细菌中或插入不同质粒中的T(6-4)T寡核苷酸在SOS诱导的SMH10大肠埃希氏菌中复制时,没有观察到这类突变。因此,这些半靶向突变是真核DNA聚合酶之一绕过COS7细胞中T(6-4)T病变的特定结果。

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