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首页> 外文期刊>Electronic Journal of Biotechnology >Analysis of genetic and epigenetic variation in in vitro propagated potato somatic hybrid by AFLP and MSAP marker
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Analysis of genetic and epigenetic variation in in vitro propagated potato somatic hybrid by AFLP and MSAP marker

机译:利用AFLP和MSAP标记分析马铃薯体细胞杂种的遗传和表观遗传变异。

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Background: Genetic and epigenetic changes (DNA methylation) were examined in the tissue-culture propagated interspecific potato somatic hybrids between dihaploid Solanum tuberosum and S. pinnatisectum. Amplified fragment length polymorphism (AFLP) and methylation-sensitive amplified polymorphism (MSAP) were applied to detect the genetic and epigenetic changes, respectively in the somatic hybrids mother plants (1st cycle) and their regenerants (30th cycles sub-cultured).Results: To detect genetic changes, eight AFLP primer combinations yielded a total of 329 scorable bands of which 49 bands were polymorphic in both mother plants and regenerants. None of the scorable bands were observed in term of loss of original band of mother plant or gain of novel band in their regenerants. AFLP profiles and their cluster analysis based on the Jaccard’s similarity coefficient revealed 100% genetic similarity among the mother plant and their regenerants. On the other hand, to analyze epigenetic changes, eight MSAP primer pair combinations detected a few DNA methylation patterns in the mother plants (0 to 3.4%) and their regenerants (3.2 to 8.5%). Out of total 2320 MSAP sites in the mother plants, 2287 (98.6%) unmethylated, 21 (0.9%) fully methylated and 12 (0.5%) hemi-methylated, and out of total 2494 MSAP sites in their regenerants, 2357 (94.5%) unmethylated, 79 (3.1%) fully methylated and 58 (2.3%) hemi-methylated sites were amplified.Conclusion: The study concluded that no genetic variations were observed among the somatic hybrids mother plants and their regenerants by eight AFLP markers. However, minimum epigenetic variations among the samples were detected ranged from 0 to 3.4% (mother plants) and 3.2 to 8.5% (regenerants) during the tissue culture process.
机译:背景:研究了在双倍体马铃薯和Pinnatisectum之间的组织培养繁殖的种间马铃薯体细胞杂种的遗传和表观遗传变化(DNA甲基化)。应用扩增片段长度多态性(AFLP)和甲基化敏感的扩增多态性(MSAP)分别检测体细胞杂种母本(第一个周期)及其再生子(传代培养的第30个周期)的遗传和表观遗传变化。为了检测遗传变化,八种AFLP引物组合产生了329条可评分带,其中49条带在母本和再生体中都是多态的。就其母体的原始条带的丧失或其再生物中的新条带的获得而言,没有观察到可评分的条带。 AFLP谱及其基于Jaccard相似系数的聚类分析表明,母本植物及其再生体之间具有100%的遗传相似性。另一方面,为了分析表观遗传变化,八种MSAP引物对组合在母本植物(0%至3.4%)及其再生体(3.2%至8.5%)中检测到一些DNA甲基化模式。在母本植物中总共2320个MSAP位点中,未甲基化的2287个(98.6%),完全甲基化的21个(0.9%)和半甲基化的12个(0.5%),在其再生体中的2494个MSAP中的2357个(94.5%) )未甲基化,扩增了79个(3.1%)完全甲基化的位点,并扩增了58个(2.3%)半甲基化的位点。结论:研究得出结论,通过8种AFLP标记未观察到体细胞杂种母株及其再生体之间的遗传变异。然而,在组织培养过程中,检测到的样品中最小的表观遗传变异范围为0至3.4%(母本植物)和3.2至8.5%(再生体)。

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