Mutational property of newly identified mutagen l-glutamic acid γ-hydrazide in Escherichia coli

IF 1.5 4区 医学 Q4 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Tomoya Maeda , Atsushi Shibai , Naomi Yokoi , Yumeko Tarusawa , Masako Kawada , Hazuki Kotani , Chikara Furusawa
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引用次数: 2

Abstract

We previously found that an l-glutamine analog l-glutamic acid γ-hydrazide has high mutagenic activity through the high-throughput laboratory evolution of Escherichia coli. In this study, mutagenicity and mutational property of l-glutamic acid γ-hydrazide were examined by the Ames test and mutation accumulation experiments using E. coli. The Ames test revealed that l-glutamic acid γ-hydrazide showed higher mutagenic activity without metabolic activation than known mutagens 2-aminoanthracene, and cobalt(II) acetate tetrahydrate. This result indicates that l-glutamic acid γ-hydrazide does not require metabolic activation for mutagenic activity in E. coli. Mutation accumulation experiments and whole-genome sequencing analysis revealed the number and spectrum of the accumulated mutations with or without l-glutamic acid γ-hydrazide. In the presence of l-glutamic acid γ-hydrazide, MDS42 strain accumulated 392.3 ± 116.2 point mutations during 30 passages corresponding to 777 generations, while MDS42 strain accumulated 1.5 ± 2.5 point mutations without l-glutamic acid γ-hydrazide during 50 passages corresponding to 1341 generations. The mutational spectrum of l-glutamic acid γ-hydrazide was G/C to A/T transition (82.2 ± 4.3 %) and A/T to G/C transition (17.4 ± 4.3 %). These results indicated that l-glutamic acid γ-hydrazide has a strong mutagenic activity.

新发现的诱变剂l-谷氨酸γ-肼在大肠杆菌中的突变特性
我们之前通过大肠杆菌的高通量实验室进化发现l-谷氨酰胺类似物l-谷氨酸γ-肼具有高诱变活性。采用Ames试验和大肠杆菌突变积累试验,研究了l-谷氨酸γ-肼的致突变性和突变特性。Ames试验表明,l-谷氨酸γ-酰肼在没有代谢激活的情况下比已知的诱变剂2-氨基蒽和四水合乙酸钴具有更高的诱变活性。结果表明,l-谷氨酸γ-酰肼不需要代谢激活就能在大肠杆菌中产生诱变活性。突变积累实验和全基因组测序分析揭示了含或不含l-谷氨酸γ-肼的累积突变的数量和谱。在存在l-谷氨酸γ-肼的条件下,MDS42菌株在30代(777代)内累积了392.3±116.2点突变,而不存在l-谷氨酸γ-肼的MDS42菌株在50代(1341代)内累积了1.5±2.5点突变。l-谷氨酸γ-酰肼的突变谱为G/C向A/T转变(82.2±4.3%),A/T向G/C转变(17.4±4.3%)。结果表明,l-谷氨酸γ-酰肼具有较强的诱变活性。
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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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