Mohd-Yusoff Nur Fatihah, Ruperao Pradeep, Tomoyoshi Nurain Emylia, Edwards David, Gresshoff Peter M, Biswas Bandana, Batley Jacqueline
Centre of Integrative Legume Research, School of Agriculture and Food Science, The University of Queensland, St Lucia, Brisbane QLD 4072, Australia Department of Cell and Molecular Biology, Faculty of Biotechnology and Biomolecular Sciences, Universiti Putra Malaysia, 43400, Serdang, Selangor, Malaysia.
Australian Centre for Plant Functional Genomics, School of Agriculture and Food Science, The University of Queensland, St Lucia, Brisbane QLD 4072, Australia Centre of Excellence in Genomics (CEG), International Crops Research Institute for the Semi-Arid Tropics (ICRISAT), Patancheru 502324, Telangana, India.
G3 (Bethesda). 2015 Feb 6;5(4):559-67. doi: 10.1534/g3.114.014571.
Genetic structure can be altered by chemical mutagenesis, which is a common method applied in molecular biology and genetics. Second-generation sequencing provides a platform to reveal base alterations occurring in the whole genome due to mutagenesis. A model legume, Lotus japonicus ecotype Miyakojima, was chemically mutated with alkylating ethyl methanesulfonate (EMS) for the scanning of DNA lesions throughout the genome. Using second-generation sequencing, two individually mutated third-generation progeny (M3, named AM and AS) were sequenced and analyzed to identify single nucleotide polymorphisms and reveal the effects of EMS on nucleotide sequences in these mutant genomes. Single-nucleotide polymorphisms were found in every 208 kb (AS) and 202 kb (AM) with a bias mutation of G/C-to-A/T changes at low percentage. Most mutations were intergenic. The mutation spectrum of the genomes was comparable in their individual chromosomes; however, each mutated genome has unique alterations, which are useful to identify causal mutations for their phenotypic changes. The data obtained demonstrate that whole genomic sequencing is applicable as a high-throughput tool to investigate genomic changes due to mutagenesis. The identification of these single-point mutations will facilitate the identification of phenotypically causative mutations in EMS-mutated germplasm.
遗传结构可通过化学诱变改变,这是分子生物学和遗传学中常用的方法。第二代测序提供了一个平台,用于揭示诱变导致的全基因组碱基变化。模式豆科植物百脉根生态型宫古岛用烷基化剂甲磺酸乙酯(EMS)进行化学诱变,以扫描全基因组的DNA损伤。利用第二代测序技术,对两个单独诱变的第三代后代(M3,命名为AM和AS)进行测序和分析,以鉴定单核苷酸多态性,并揭示EMS对这些突变基因组中核苷酸序列的影响。在每208 kb(AS)和202 kb(AM)中发现单核苷酸多态性,G/C到A/T的偏向性突变比例较低。大多数突变位于基因间。基因组的突变谱在其各个染色体中具有可比性;然而,每个突变基因组都有独特的变化,这有助于识别其表型变化的因果突变。所获得的数据表明,全基因组测序可作为一种高通量工具,用于研究诱变导致的基因组变化。这些单点突变的鉴定将有助于在EMS诱变种质中鉴定表型因果突变。