Gentil A, Le Page F, Margot A, Lawrence C W, Borden A, Sarasin A
Institut de Recherches sur le Cancer, CNRS, IFC 1, Laboratory of Molecular Genetics, Villejuif, France.
Nucleic Acids Res. 1996 May 15;24(10):1837-40. doi: 10.1093/nar/24.10.1837.
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.
利用穿梭载体在哺乳动物细胞中研究了紫外线诱导的光产物的诱变特性,包括顺式-胸腺嘧啶二聚体(TT)和胸腺嘧啶-胸腺嘧啶嘧啶酮(6-4)光产物 [T(6-4)T]。构建了一种能在哺乳动物细胞和细菌中都能复制的穿梭载体,以单链DNA形式存在。在单一限制性位点插入一个独特的光产物,单链DNA载体环化后,将其转染到猴COS7细胞中。DNA复制后,从细胞中提取载体并用于转化细菌。最终对扩增的DNA进行分析,无需任何选择性筛选,直接对随机挑选的细菌菌落的DNA进行测序。我们的结果清楚地表明,这两种损伤都是诱变的,但程度不同。TT二聚体和T(6-4)T的突变频率分别为2%和60%。对于TT二聚体,突变靶向于3'-T。对于T(6-4)T,观察到多种突变。大多数G→T颠换半靶向于光产物5'-T之前的碱基。当将相同质粒直接转染到SOS诱导的JM105细菌中,或者当插入不同质粒中的T(6-4)T寡核苷酸在SOS诱导的SMH10大肠杆菌中复制时,未观察到这类突变。因此,这些半靶向突变是真核DNA聚合酶之一在COS7细胞中绕过T(6-4)T损伤的特定结果。