Identification and characterization of inheritable structural variations induced by ion beam radiations in rice

IF 1.5 4区 医学 Q4 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Yunchao Zheng , Shan Li , Jianzhong Huang , Haowei Fu , Libin Zhou , Yoshiya Furusawa , Qingyao Shu
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引用次数: 5

Abstract

High energy ion beams are effective physical mutagens for mutation induction in plants. Due to their high linear energy transfer (LET) property, they are known to generate single nucleotide variations (SNVs) and insertion/deletions (InDels, <50 bp) as well as structural variations (SVs). However, due to the technical difficulties to identify SVs, studies on ion beam induced SVs by genome sequencing have so far been limited in numbers and inadequate in nature, and knowledge of SVs is scarce with regards to their characteristics. In the present study, we identified and validated SVs in six M4 plants (designated as Ar_50, Ar_100, C_150, C_200, Ne_50 and Ne_100 according to ion beam types and irradiation doses), two each induced by argon (40Ar18+), carbon (12C6+) and neon (20Ne10+) ion beams and performed in depth analyses of their characteristics. In total, 22 SVs were identified and validated, consisting of 11 deletions, 1 duplication, and 4 intra-chromosomal and 6 inter-chromosomal translocations. There were several SVs larger than 1 kbp. The SVs were distributed across the whole genome with an aggregation with SNVs and InDels only in the Ne_50 mutants. An enrichment of a 11-bp wide G-rich DNA motif 'GAAGGWGGRGG' was identified around the SV breakpoints. Three mechanisms might be involved in the SV formation, i.e., the expansion of tandem repeats, transposable element insertion, and non-allelic homologous recombination. Put together, the present study provides a preliminary view of SVs induced by Ar, C and Ne ion beam radiations, and as a pilot study, it contributes to our understanding of how SVs might form after ion beam irradiation in rice.

离子束辐射诱导水稻遗传结构变异的鉴定与表征
高能离子束是植物诱变的有效物理诱变剂。由于其高线性能量转移(LET)特性,已知它们会产生单核苷酸变异(snv)和插入/缺失(InDels, <50 bp)以及结构变异(SVs)。然而,由于对sv的鉴定技术困难,迄今为止离子束诱导sv的基因组测序研究数量有限,性质不充分,对sv的特性了解较少。在本研究中,我们对6株M4植物(根据离子束类型和辐照剂量分别命名为Ar_50、Ar_100、C_150、C_200、Ne_50和Ne_100)中的SVs进行了鉴定和验证,其中氩(40Ar18+)、碳(12C6+)和氖(20Ne10+)离子束诱导的SVs各2株,并对其特性进行了深入分析。共鉴定和验证了22个sv,包括11个缺失,1个重复,4个染色体内易位和6个染色体间易位。有几个sv大于1kbp。sv分布于整个基因组,仅在Ne_50突变体中与snv和indel聚集。在SV断点附近发现了一个11 bp宽的富g DNA基序“gaaggwgggg”的富集。SV的形成可能涉及三种机制,即串联重复序列的扩展、转座因子的插入和非等位基因同源重组。综上所述,本研究提供了Ar、C和Ne离子束辐照诱导水稻SVs的初步认识,并作为一项先导研究,有助于我们了解离子束辐照后水稻SVs的形成机制。
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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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