Inducing mutation and ascertaining lethal dosage of in vitro cultures of banana cv. Ney Poovan to ethyl methane sulfonate

IF 1.5 4区 医学 Q4 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Mutation Research-Fundamental and Molecular Mechanisms of Mutagenesis Pub Date : 2024-01-01 DOI:10.1016/j.mrfmmm.2023.111850
C.Y. Shalini Udaya
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Abstract

In vitro mutation breeding in vegetatively propagated crops like banana offers a benefit in screening for beneficial variants in plant cells or cultured tissues. An attempt was made to induce mutants and determine the lethal dose, as it is the prerequisite to optimize the concentration and duration of the mutagen used to recover a larger population in mutation research. Shoot tip cultures were treated for 2 and 4 h at six different EMS concentrations ranging from 80 mM to 160 mM, whereas proliferating multiple shoots were exposed for 30 and 60 min at six different EMS concentrations ranging from 8 mM to 40 mM. Survival percentage, shoot length, and number of shoots reduced linearly and significantly as concentration and duration increased in both shoot tips and proliferating multiple buds. The probit curve-based analysis of mortality of treated explants revealed that the LD50 was 155.83 mM for 2 h and 113.72 mM for 4 h, respectively for shoot tip cultures, whereas for proliferating multiple buds, the LD50 value was adjusted to 39.11 mM for 30 min and 30.41 mM for 60 min. 160 mM EMS for 4 h resulted in a shorter shoot, a longer rooting duration, a lesser number of roots, and decreased root development. In proliferating multiple shoots, the smallest shoot, longest rooting duration, least number of roots, and shortest root were observed in 40 mM EMS for 60 min. Similar reductions in growth parameters were observed in proliferating multiple shoots at higher exposure to EMS for a longer duration.

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诱导香蕉变种 Ney Poovan 对甲烷磺酸乙酯的体外培养变异并确定致死剂量
香蕉等无性繁殖作物的体外诱变育种有利于在植物细胞或培养组织中筛选有益变体。我们尝试诱导突变体并确定致死剂量,因为这是优化诱变剂浓度和持续时间的先决条件,以便在突变研究中恢复更大的群体。芽尖培养物在 80 mM 至 160 mM 的六种不同 EMS 浓度下分别处理 2 小时和 4 小时,而增殖的多芽则在 8 mM 至 40 mM 的六种不同 EMS 浓度下分别暴露 30 分钟和 60 分钟。随着浓度和持续时间的增加,芽尖和增殖多芽的存活率、芽长和芽数都呈线性显著下降。基于 probit 曲线的外植体死亡率分析表明,对于芽尖培养物,2 小时和 4 小时的半数致死剂量分别为 155.83 毫摩尔和 113.72 毫摩尔;而对于增殖多芽,30 分钟和 60 分钟的半数致死剂量分别为 39.11 毫摩尔和 30.41 毫摩尔。160 毫摩尔 EMS 4 小时会导致芽变短、生根时间延长、根数量减少和根系发育减弱。在增殖的多芽中,40 毫摩尔 EMS 60 分钟的芽最小、生根时间最长、根数最少、根最短。在较长时间暴露于 EMS 的情况下,增殖多芽的生长参数也出现了类似的下降。
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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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