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离子束诱变突变体的基因组测序有助于检测候选基因,这些基因负责水稻突变体表型。

Genome sequencing of ion-beam-induced mutants facilitates detection of candidate genes responsible for phenotypes of mutants in rice.

机构信息

Department of Radiation-Applied Biology Research, Takasaki Advanced Radiation Research Institute (TARRI), Quantum Beam Science Research Directorate (QuBS), National Institutes for Quantum and Radiological Science and Technology (QST), Takasaki, Gunma, Japan.

Ion Beam Breeding Team, RIKEN Nishina Center for Accelerator-Based Science (RNC), RIKEN, Wako, Saitama, Japan.

出版信息

Mutat Res. 2020 May-Dec;821:111691. doi: 10.1016/j.mrfmmm.2020.111691. Epub 2020 Feb 21.

Abstract

Ion beams are physical mutagens used for plant and microbe breeding that cause mutations via a mechanism distinct from those of chemical mutagens or gamma rays. We utilized whole-exome sequencing of rice DNA in order to understand the properties of ion beam-induced mutations in a genome-wide manner. DNA libraries were constructed from selected carbon-ion-beam-induced rice mutants by capturing with a custom probes covering 66.3 M bases of nearly all exons and miRNAs predicted in the genome. A total of 56 mutations, including 24 single nucleotide variations, 23 deletions, and 5 insertions, were detected in five mutant rice lines (two dwarf and three early-heading-date mutants). The mutations were distributed among all 12 chromosomes, and the average mutation frequency in the M1 generation was estimated to be 2.7 × 10 per base. Many single base insertions and deletions were associated with homopolymeric repeats, whereas larger deletions up to seven base pairs were observed at polynucleotide repeats in the DNA sequences of the mutation sites. Of the 56 mutations, six were classified as high-impact mutations that caused a frame shift or loss of exons. A gene that was functionally related to the phenotype of the mutant was disrupted by a high-impact mutation in four of the five lines tested, suggesting that whole-exome sequencing of ion-beam-irradiated mutants could facilitate the detection of candidate genes responsible for the mutant phenotypes.

摘要

离子束是用于植物和微生物育种的物理诱变剂,通过与化学诱变剂或伽马射线不同的机制引起突变。我们利用水稻 DNA 的全外显子组测序,以便全面了解离子束诱导突变在基因组中的特性。通过用覆盖基因组中几乎所有外显子和预测的 miRNA 的定制探针捕获,从选定的碳离子束诱导的水稻突变体中构建 DNA 文库。在五个突变体水稻品系(两个矮秆和三个早穗突变体)中检测到 56 个突变,包括 24 个单核苷酸变异、23 个缺失和 5 个插入。突变分布在所有 12 条染色体上,M1 代的平均突变频率估计为每碱基 2.7×10。许多单碱基插入和缺失与同聚体重复有关,而在突变位点的 DNA 序列中观察到长达七个碱基对的较大缺失则发生在多核苷酸重复处。在 56 个突变中,有 6 个被归类为高影响突变,导致移码或外显子缺失。在测试的五个品系中的四个中,一个与突变体表型功能相关的基因被高影响突变所破坏,这表明对离子束辐照突变体的全外显子组测序可以促进候选基因的检测,这些候选基因与突变体表型有关。

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