Doetsch Paul W
Department of Biochemistry and Division of Cancer Biology, Emory University School of Medicine, 4013 Rollins Research Center, Atlanta, GA 30322, USA.
Mutat Res. 2002 Dec 29;510(1-2):131-40. doi: 10.1016/s0027-5107(02)00258-0.
The genes of all organisms are continuously damaged by extrinsic and intrinsic physical and chemical agents. If the resulting DNA damage is left unrepaired, a number of deleterious biological consequences may result including the production of mutant proteins which can change the cellular phenotype. The majority of DNA damage-induced mutagenesis studies are based on models of DNA polymerase errors occurring in the vicinity of the lesion. In contrast, few studies have addressed the possibility that mutagenesis at the level of transcription (i.e. when RNA polymerase bypasses a lesion and a misincorporation event occurs) may also be an important source of mutant proteins, particularly in nondividing cell populations. This article reviews a number of recent studies on translesion synthesis by RNA polymerases resulting in the production of mutant transcripts (transcriptional mutagenesis). Over a dozen different types of DNA damage are now known to be bypassed with various degrees of efficiency and miscoding abilities by the transcriptional elongation machinery. Some important biological implications of transcriptional mutagenesis are discussed.
所有生物体的基因都会持续受到外在和内在物理及化学因素的损伤。如果由此产生的DNA损伤未得到修复,可能会导致一些有害的生物学后果,包括产生能够改变细胞表型的突变蛋白。大多数DNA损伤诱导的诱变研究是基于损伤附近发生的DNA聚合酶错误模型。相比之下,很少有研究探讨转录水平诱变(即当RNA聚合酶绕过损伤并发生错配事件时)也可能是突变蛋白的重要来源这一可能性,特别是在非分裂细胞群体中。本文综述了一些关于RNA聚合酶跨损伤合成导致突变转录本产生(转录诱变)的最新研究。现已知道,转录延伸机制能够以不同程度的效率和错编能力绕过十几种不同类型的DNA损伤。文中还讨论了转录诱变的一些重要生物学意义。