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Analysis of genetic and epigenetic variation in in vitro propagated potato somatic hybrid by AFLP and MSAP marker

机译:AFLP和MSAP标记物体外繁殖马铃薯体细胞杂交体遗传和表观遗传变异分析

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摘要

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:基因,并在组织培养检查表观遗传改变(DNA甲基化)传播双单倍体马铃薯和S. pinnatisectum种间马铃薯体细胞杂种。扩增片段长度多态性(AFLP)和甲基化敏感性扩增多态性(MSAP)施用于检测遗传和表观遗传变化,分别在体细胞杂种母株(第一循环)和它们的再生体(第30次循环传代培养)。结果:为了检测遗传变化,八个AFLP引物组合总共329个可评分频带其中49条带中既母株和再生体多态性的产生。在母亲工厂或在他们的再生植株的新乐队的增益的原创乐队的损失的长期观察刻痕带无。 AFLP配置文件和基于该捷卡的相似系数的聚类分析显示母株及其再生剂中100%的遗传相似性。在另一方面,为了分析表观遗传变化,八个MSAP引物对的组合检测到母株(0到3.4%)和它们的再生体(3.2至8.5%)的几个DNA甲基化模式。在外面的母株共2320个MSAP网站,2287(98.6%)未甲基化,21(0.9%)完全甲基化和12(0.5%)的半甲基化,并出他们的再生植株共2494 MSAP网站,2357(94.5% )未甲基化的,79(3.1%)全甲基化和58(2.3%)半甲基化的位点扩增。结论:该研究的结论是,体细胞杂种母株及其再生植株中观察到八个AFLP标记没有遗传变异。然而,样品间的最小变化后生检测范围从0到在组织培养过程中的3.4%(母株)和3.2至8.5%(再生剂)。

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