Miller J H
Department of Microbiology and Molecular Genetics, University of California, Los Angeles 90024, USA.
Cancer Surv. 1996;28:141-53.
The study of mutator strains of bacteria has elucidated new systems and pathways of mutagenesis and led to the defining of human counterparts to these systems. In addition to previous work that defined the mismatch repair system, newer studies have revealed a repair pathway for oxidative lesions, as well as demonstrating that mistranslation can increase mutation rates. Defects in the human repair pathways are involved in increased cancer susceptibility as well as a mutator character.
对细菌突变菌株的研究阐明了新的诱变系统和途径,并促成了这些系统在人类中的对应物的定义。除了先前定义错配修复系统的工作之外,更新的研究还揭示了一种针对氧化性损伤的修复途径,同时也证明了错误翻译会增加突变率。人类修复途径中的缺陷与癌症易感性增加以及一种突变特性有关。