Loechler E L
Department of Biology, Boston University, MA 02215, USA.
Carcinogenesis. 1996 May;17(5):895-902. doi: 10.1093/carcin/17.5.895.
Usually, a particular mutagen/carcinogen forms adducts at many sites in DNA, making it impossible to determine which type of adduct causes which mutation and why. Adduct site-specific mutagenesis studies, in which a single adduct is built into a vector, can be used to overcome this problem. The adduct can be situated in double-stranded DNA, single-stranded DNA or in a single-stranded gap, and the benefit and concerns associated with each are addressed. An adduct site-specific study is most useful when it is compared to a mutagenesis study with its corresponding mutagen/carcinogen. Mutations induced by a particular mutagen/carcinogen can be influenced by DNA sequence context, mutagen/carcinogen dose (and other changes in conditions), level of SOS induction, cell type and other factors. Thus, it is important to match the conditions of the adduct study versus the mutagen/carcinogen study as closely as possible. DNA sequence context can profoundly affect the quantitative and qualitative pattern of adduct mutagenesis, which is addressed. In vitro studies with DNA polymerases, frameshift mutagenesis and semi-targeted mutagenesis, whereby a mutation is induced near but not at the site of the adduct, are each discussed. Finally, the relationship between structural studies on adducts and mutagenesis is considered.
通常,一种特定的诱变剂/致癌物会在DNA的多个位点形成加合物,这使得无法确定哪种类型的加合物会导致哪种突变以及原因。加合物位点特异性诱变研究可以用来克服这个问题,在这种研究中,单个加合物被构建到载体中。该加合物可以位于双链DNA、单链DNA或单链缺口处,文中讨论了每种情况的益处和相关问题。当将加合物位点特异性研究与其相应的诱变剂/致癌物的诱变研究进行比较时,这种研究最为有用。特定诱变剂/致癌物诱导的突变可能会受到DNA序列背景、诱变剂/致癌物剂量(以及其他条件变化)、SOS诱导水平、细胞类型和其他因素的影响。因此,尽可能使加合物研究与诱变剂/致癌物研究的条件相匹配非常重要。文中讨论了DNA序列背景如何深刻影响加合物诱变的定量和定性模式。还分别讨论了使用DNA聚合酶的体外研究、移码诱变和半靶向诱变(即在加合物位点附近而非该位点诱导突变)。最后,考虑了加合物结构研究与诱变之间的关系。