{"title":"Properties and functions of Escherichia coli: Pol IV and Pol V.","authors":"Robert P Fuchs, Shingo Fujii, Jérôme Wagner","doi":"10.1016/S0065-3233(04)69008-5","DOIUrl":null,"url":null,"abstract":"<p><p>Escherichia coli possesses two members of the newly discovered class of Y DNA polymerases (Ohmori et al., 2001): Pol IV (dinB) and Pol V (umuD'C). Polymerases that belong to this family are often referred to as specialized or error-prone DNA polymerases to distinguish them from the previously discovered DNA polymerases (Pol I, II, and III) that are essentially involved in DNA replication or error-free DNA repair. Y-family DNA polymerases are characterized by their capacity to replicate DNA, through chemically damaged template bases, or to elongate mismatched primer termini. These properties stem from their capacity to accommodate and use distorted primer templates within their active site and from the lack of an associated exonuclease activity. Even though both belong to the Y-family, Pol IV and Pol V appear to perform distinct physiological functions. Although Pol V is clearly the major lesion bypass polymerase involved in damage-induced mutagenesis, the role of Pol IV remains enigmatic. Indeed, compared to a wild-type strain, a dinB mutant exhibits no clear phenotype with respect to survival or mutagenesis following treatment with DNA-damaging agents. Subtler dinB phenotypes will be discussed below. Moreover, despite the fact that both dinB and umuDC loci are controlled by the SOS response, their constitutive and induced levels of expression are dramatically different. In noninduced cells, Pol V is undetectable by Western analysis. In contrast, it is estimated that there are about 250 copies of Pol IV per cell. On SOS induction, it is believed that only about 15 molecules of Pol V are assembled per cell (S. Sommer, personal communication), whereas Pol IV levels reach approximately 2500 molecules. In fact, despite extensive knowledge of the individual enzymatic properties of all five E. coli DNA polymerases, much more work is needed to understand how their activities are orchestrated within a living cell.</p>","PeriodicalId":51216,"journal":{"name":"Advances in Protein Chemistry","volume":"69 ","pages":"229-64"},"PeriodicalIF":0.0000,"publicationDate":"2004-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0065-3233(04)69008-5","citationCount":"94","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advances in Protein Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1016/S0065-3233(04)69008-5","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 94
Abstract
Escherichia coli possesses two members of the newly discovered class of Y DNA polymerases (Ohmori et al., 2001): Pol IV (dinB) and Pol V (umuD'C). Polymerases that belong to this family are often referred to as specialized or error-prone DNA polymerases to distinguish them from the previously discovered DNA polymerases (Pol I, II, and III) that are essentially involved in DNA replication or error-free DNA repair. Y-family DNA polymerases are characterized by their capacity to replicate DNA, through chemically damaged template bases, or to elongate mismatched primer termini. These properties stem from their capacity to accommodate and use distorted primer templates within their active site and from the lack of an associated exonuclease activity. Even though both belong to the Y-family, Pol IV and Pol V appear to perform distinct physiological functions. Although Pol V is clearly the major lesion bypass polymerase involved in damage-induced mutagenesis, the role of Pol IV remains enigmatic. Indeed, compared to a wild-type strain, a dinB mutant exhibits no clear phenotype with respect to survival or mutagenesis following treatment with DNA-damaging agents. Subtler dinB phenotypes will be discussed below. Moreover, despite the fact that both dinB and umuDC loci are controlled by the SOS response, their constitutive and induced levels of expression are dramatically different. In noninduced cells, Pol V is undetectable by Western analysis. In contrast, it is estimated that there are about 250 copies of Pol IV per cell. On SOS induction, it is believed that only about 15 molecules of Pol V are assembled per cell (S. Sommer, personal communication), whereas Pol IV levels reach approximately 2500 molecules. In fact, despite extensive knowledge of the individual enzymatic properties of all five E. coli DNA polymerases, much more work is needed to understand how their activities are orchestrated within a living cell.
大肠杆菌拥有两种新发现的Y DNA聚合酶(Ohmori et al., 2001): Pol IV (dinB)和Pol V (umuD'C)。属于该家族的聚合酶通常被称为特化或易出错DNA聚合酶,以区别于先前发现的DNA聚合酶(Pol I, II和III),这些聚合酶主要参与DNA复制或无错误DNA修复。y家族DNA聚合酶的特点是它们能够复制DNA,通过化学损伤的模板碱基,或延长不匹配的引物末端。这些特性源于它们在活性位点内容纳和使用扭曲引物模板的能力,以及缺乏相关的外切酶活性。尽管两者都属于y家族,但Pol IV和Pol V似乎具有不同的生理功能。虽然Pol V显然是参与损伤诱变的主要病变旁路聚合酶,但Pol IV的作用仍然是谜。事实上,与野生型菌株相比,在dna损伤剂治疗后,dinB突变体在存活或突变方面没有明确的表型。下面将讨论更微妙的dinB表型。此外,尽管dinB和umuDC基因座都受SOS反应控制,但它们的构成和诱导表达水平却有很大不同。在非诱导细胞中,用Western分析无法检测到Pol V。相比之下,据估计每个细胞约有250个Pol IV拷贝。在SOS诱导下,每个细胞只组装约15个Pol V分子(S. Sommer,个人通信),而Pol IV水平达到约2500个分子。事实上,尽管对所有五种大肠杆菌DNA聚合酶的单个酶特性有广泛的了解,但要了解它们在活细胞内的活动是如何协调的,还需要做更多的工作。