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精确评估组织培养在大麦体外再生体系优化过程中引起的变异。

Precise evaluation of tissue culture-induced variation during optimisation of in vitro regeneration regime in barley.

机构信息

Department of Plant Physiology and Biochemistry, Plant Breeding and Acclimatization Institute-National Research Institute, Błonie, 05-870, Radzików, Poland.

出版信息

Plant Mol Biol. 2020 May;103(1-2):33-50. doi: 10.1007/s11103-020-00973-5. Epub 2020 Feb 11.

Abstract

The Taguchi method and metAFLP analysis were used to optimise barley regenerants towards maximum and minimum levels of tissue culture-induced variation. The subtle effects of symmetric and asymmetric methylation changes in regenerants were identified. Plant tissue cultures (PTCs) provide researchers with unique materials that accelerate the development of new breeding cultivars and facilitate studies on off-type regenerants. The emerging variability of regenerants derived from PTCs may have both genetic and epigenetic origins, and may be desirable or degrade the value of regenerated plants. Thus, it is crucial to determine how the PTC variation level can be controlled. The easiest way to manipulate total tissue culture-induced variation (TTCIV) is to utilise appropriate stress factors and suitable medium components. This study describes the optimisation of in vitro tissue culture-induced variation in plant regenerants derived from barley anther culture, and maximizes and minimizes regenerant variation compared with the source explants. The approach relied on methylation amplified fragment length polymorphism (metAFLP)-derived TTCIV characteristics, which were evaluated in regenerants derived under distinct tissue culture conditions and analysed via Taguchi statistics. The factors that may trigger TTCIV included CuSO, AgNO and the total time spent on the induction medium. The donor plants prepared for regeneration purposes had 5.75% and 2.01% polymorphic metAFLP loci with methylation and sequence changes, respectively. The level of TTCIV (as the sum of all metAFLP characteristics analyzed) identified in optimisation and verification experiments reached 7.51 and 10.46%, respectively. In the trial designed to produce a minimum number of differences between donor and regenerant plants, CuSO and AgNO were more crucial than time, which was not a significant factor. In the trial designed to produce a maximum number of differences between donor and regenerant plants, all factors had comparable impact on variation. The Taguchi method reduced the time required for experimental trials compared with a grid method and suggested that medium modifications were required to control regenerant variation. Finally, the effects of symmetric and asymmetric methylation changes on regenerants were identified using novel aspects of the metAFLP method developed for this analysis.

摘要

采用田口法和 metAFLP 分析优化大麦再生体,以达到组织培养诱导变异的最大和最小水平。鉴定了再生体中对称和非对称甲基化变化的细微影响。植物组织培养(PTCs)为研究人员提供了独特的材料,加速了新的育种品种的开发,并促进了异常再生体的研究。源自 PTC 的再生体的新兴可变性可能具有遗传和表观遗传起源,并且可能是期望的或降低再生植物的价值。因此,确定如何控制 PTC 变异水平至关重要。操纵总组织培养诱导变异(TTCIV)的最简单方法是利用适当的应激因素和合适的培养基成分。本研究描述了优化来自大麦花药培养的植物再生体的体外组织培养诱导变异,并与源外植体相比最大化和最小化再生体变异。该方法依赖于甲基化扩增片段长度多态性(metAFLP)衍生的 TTCIV 特征,这些特征在不同组织培养条件下衍生的再生体中进行评估,并通过田口统计进行分析。可能触发 TTCIV 的因素包括 CuSO4、AgNO3 和诱导培养基上花费的总时间。为再生目的制备的供体植物分别具有 5.75%和 2.01%的多态性 metAFLP 位点,分别具有甲基化和序列变化。在优化和验证实验中鉴定的 TTCIV 水平(作为分析的所有 metAFLP 特征的总和)分别达到 7.51%和 10.46%。在设计产生供体和再生植物之间最小数量差异的试验中,CuSO4 和 AgNO3 比时间更为关键,时间不是重要因素。在设计产生供体和再生植物之间最大数量差异的试验中,所有因素对变异都有类似的影响。田口法与网格法相比,减少了实验试验所需的时间,并表明需要对培养基进行修改以控制再生体变异。最后,使用为该分析开发的 metAFLP 方法的新方面,鉴定了对称和非对称甲基化变化对再生体的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6aa8/7170832/093205ba3faa/11103_2020_973_Fig1_HTML.jpg

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