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Use of Combined MSAP and NGS Techniques to Identify Differentially Methylated Regions in Somaclones: A Case Study of Two Stable Somatic Wheat Mutants

机译:结合使用MSAP和NGS技术鉴定Somaclone中的甲基化差异区域:两个稳定的体细胞小麦突变体的案例研究

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摘要

The appearance of somaclonal variability induced by in vitro cultivation is relatively frequent and can, in some cases, provide a valuable source of new genetic variation for crop improvement. The cause of this phenomenon remains unknown; however, there are a number of reports suggesting that epigenetics, including DNA methylations, are an important factor. In addition to the non-heritable DNA methylation changes caused by transient and reversible stress-responsive gene regulation, recent evidence supports the existence of mitotically and meiotically inherited changes. The induction of phenotypes via stable DNA methylation changes has occasionally great economical value; however, very little is known about the genetic or molecular basis of these phenotypes. We used a novel approach consisting of a standard MSAP analysis followed by deep amplicon sequencing to better understand this phenomenon. Our models included two wheat genotypes, and their somaclones induced using in vitro cultivation with a changed heritable phenotype (shortened stem height and silenced high molecular weight glutenin). Using this novel procedure, we obtained information on the dissimilarity of DNA methylation landscapes between the standard cultivar and its respective somaclones, and we extracted the sequences and genome regions that were differentially methylated between subjects. Transposable elements were identified as the most likely factor for producing changes in somaclone properties. In summary, the novel approach of combining MSAP and NGS is relatively easy and widely applicable, which is a rather unique feature compared with the currently available techniques in the epigenetics field.
机译:体外培养引起的体细胞无定形变异的出现相对频繁,在某些情况下,可以为作物改良提供新的遗传变异的宝贵来源。这种现象的原因仍然未知。但是,有许多报告表明,表观遗传学(包括DNA甲基化)是重要因素。除了由瞬时和可逆的应激反应基因调控引起的不可遗传的DNA甲基化变化外,最近的证据支持有丝分裂和减数分裂遗传改变的存在。通过稳定的DNA甲基化变化诱导表型有时具有很大的经济价值。然而,关于这些表型的遗传或分子基础知之甚少。我们使用了一种新颖的方法,包括标准的MSAP分析和随后的深度扩增子测序,以更好地了解这种现象。我们的模型包括两种小麦基因型,它们的体细胞克隆是通过体外培养诱导的,具有可改变的遗传表型(缩短茎高和沉默高分子量谷蛋白)。使用这种新颖的方法,我们获得了有关标准品种与其相应的体细胞克隆之间DNA甲基化景观差异的信息,并提取了受试者之间甲基化差异的序列和基因组区域。转座因子被确定为造成somaclone特性变化的最可能因素。总而言之,结合MSAP和NGS的新颖方法相对容易并且广泛适用,与表观遗传学领域中当前可用的技术相比,这是一个相当独特的功能。

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