产生不同紫外线诱导突变光谱的生化和光化学机制

IF 1.5 4区 医学 Q4 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Mutation Research-Fundamental and Molecular Mechanisms of Mutagenesis Pub Date : 2021-07-01 DOI:10.1016/j.mrfmmm.2021.111762
Tomohiko Sugiyama , Brianna Keinard , Griffin Best , Mahima R. Sanyal
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引用次数: 4

摘要

虽然紫外线诱变已被广泛研究,但将紫外线诱导的DNA损伤转化为突变的确切机制仍然难以捉摸。一个被充分研究的机制涉及DNA聚合酶(Pol) η和ζ,它们产生C >跨嘧啶二聚体的平移合成(TLS)中的T跃迁。我们之前提出了另一种生化机制,涉及多次紫外线照射,中间在黑暗中孵育。孵育促进嘧啶二聚体中胞嘧啶的自发脱氨,随后的紫外线照射诱导不依赖光解酶的(直接)光逆转,将胞嘧啶转化为单体尿嘧啶残基。在本文中,我们首次证明了自然阳光可以在体外诱导这两个突变过程。用单色UVB在300 nm波长下也能再现直接光反转。我们还证明了两个突变过程都需要在黑暗中进行辐照后孵育,这表明在Pol η/ζ依赖和光逆转依赖的机制中都需要胞嘧啶脱胺。当与Pol ζ结合时,另一个y家族聚合酶Pol ι也介导了紫外线损伤模板上的诱变TLS。Pol -依赖性突变在很大程度上与辐照后孵育无关,这表明胞嘧啶脱氨作用不是该突变过程所必需的。阳光照射也会诱发C >一种可能由鸟嘌呤残基氧化引起的翻转。最后,我们以一种与癌症突变特征类似的格式构建了体外突变谱。虽然Pol - η依赖和光逆转依赖的光谱与癌症特征(SBS7a)高度相似,但Pol -ⅰ依赖的突变光谱具有不同的T >A/C替换,在另一种癌症特征(SBS7d)中发现。Pol依赖性T >A/C取代对T4嘧啶二聚体糖基化酶具有抗性,表明该突变过程与顺-syn嘧啶二聚体无关。讨论了紫外线诱变的多种机制的最新模型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Biochemical and photochemical mechanisms that produce different UV-induced mutation spectra

Although UV-induced mutagenesis has been studied extensively, the precise mechanisms that convert UV-induced DNA damage into mutations remain elusive. One well-studied mechanism involves DNA polymerase (Pol) η and ζ, which produces C > T transitions during translesion synthesis (TLS) across pyrimidine dimers. We previously proposed another biochemical mechanism that involves multiple UV-irradiations with incubation in the dark in between. The incubation facilitates spontaneous deamination of cytosine in a pyrimidine dimer, and the subsequent UV irradiation induces photolyase-independent (direct) photoreversal that converts cytosine into monomeric uracil residue. In this paper, we first demonstrate that natural sunlight can induce both mutational processes in vitro. The direct photoreversal was also reproduced by monochromatic UVB at 300 nm. We also demonstrate that post-irradiation incubation in the dark is required for both mutational processes, suggesting that cytosine deamination is required for both the Pol η/ζ-dependent and the photoreversal-dependent mechanisms. Another Y-family polymerase Pol ι also mediated a mutagenic TLS on UV-damaged templates when combined with Pol ζ. The Pol ι-dependent mutations were largely independent of post-irradiation incubation, indicating that cytosine deamination was not essential for this mutational process. Sunlight-exposure also induced C > A transversions which were likely caused by oxidation of guanine residues. Finally, we constructed in vitro mutation spectra in a comparable format to cancer mutation signatures. While both Pol η-dependent and photoreversal-dependent spectra showed high similarities to a cancer signature (SBS7a), Pol ι-dependent mutation spectrum has distinct T > A/C substitutions, which are found in another cancer signature (SBS7d). The Pol ι-dependent T > A/C substitutions were resistant to T4 pyrimidine dimer glycosylase-treatment, suggesting that this mutational process is independent of cis-syn pyrimidine dimers. An updated model about multiple mechanisms of UV-induced mutagenesis is discussed.

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来源期刊
CiteScore
4.90
自引率
0.00%
发文量
24
审稿时长
51 days
期刊介绍: Mutation Research (MR) provides a platform for publishing all aspects of DNA mutations and epimutations, from basic evolutionary aspects to translational applications in genetic and epigenetic diagnostics and therapy. Mutations are defined as all possible alterations in DNA sequence and sequence organization, from point mutations to genome structural variation, chromosomal aberrations and aneuploidy. Epimutations are defined as alterations in the epigenome, i.e., changes in DNA methylation, histone modification and small regulatory RNAs. MR publishes articles in the following areas: Of special interest are basic mechanisms through which DNA damage and mutations impact development and differentiation, stem cell biology and cell fate in general, including various forms of cell death and cellular senescence. The study of genome instability in human molecular epidemiology and in relation to complex phenotypes, such as human disease, is considered a growing area of importance. Mechanisms of (epi)mutation induction, for example, during DNA repair, replication or recombination; novel methods of (epi)mutation detection, with a focus on ultra-high-throughput sequencing. Landscape of somatic mutations and epimutations in cancer and aging. Role of de novo mutations in human disease and aging; mutations in population genomics. Interactions between mutations and epimutations. The role of epimutations in chromatin structure and function. Mitochondrial DNA mutations and their consequences in terms of human disease and aging. Novel ways to generate mutations and epimutations in cell lines and animal models.
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