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首页> 外文期刊>Acta Biologica Szegediensis >Molecular and genome size analyses of somaclonal variation in apple rootstocks Malling 7 and Malling 9
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Molecular and genome size analyses of somaclonal variation in apple rootstocks Malling 7 and Malling 9

机译:苹果砧木Malling 7和Malling 9体细胞克隆变异的分子和基因组大小分析

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The cultivated apple (Malus domestica) is important fruit crops cultivated inworld. For production and breeding of high quality apple, inducing and enhancing new geneticdiversity and suitable traits are necessary. In Iran, different local and imported apple genotypesare cultivated and common apple root stocks (Malling 7) M7 and (Malling 9) M9 are mostly usedroot stocks in the country. Therefore, we studied genetic diversity of M7 an M9 tissue cultureregenerated plants produced by different treatments by using twenty ISSR markers. In total51 randomly selected plants were studied for the occurrence of somaclonal variation in applemother plants and tissue culture regenerated plants. Four different treatments were used fortissue culture. Genetic diversity parameters, genetic distance and polymorphism percentagewere studied in regenerated plants. Variations in loci frequency and combination were checkedby STRUCTURE and the presence of similar loci in the plants was studied by reticulation NJ tree.Genetic relationship versus distinctness was determined by principal coordinate analysis. Theresults showed the occurrence of genetic variation among mother plants and tissue culture regeneratedplants of each subculture due to somaclonal variation. Significant difference in thegenome size among some of the regenerated plants indicates that change in genetic structureof plants during tissue culture is also accompanied with quantitative change in DNA. However,degree of genetic variation differed among apple rootstocks and also among different treatmentsused.
机译:栽培苹果(Malus domestica)是世界上重要的水果作物。为了生产和育种优质苹果,必须诱导和增强新的遗传多样性和合适的性状。在伊朗,种植了不同的本地和进口苹果基因型,在该国,常见的苹果根系种群(Malling 7)M7和(Malling 9)M9主要用作根系种群。因此,我们使用二十种ISSR标记研究了通过不同处理产生的M7和M9组织培养再生植物的遗传多样性。总共研究了51种随机选择的植物在苹果母植物和组织培养再生植物中体细胞克隆变异的发生。在组织培养中使用了四种不同的处理方法。研究了再生植物的遗传多样性参数,遗传距离和多态性百分比。通过结构检查基因座频率和组合的变化,并通过网状NJ树研究植物中类似基因座的存在。通过主坐标分析确定遗传关系与不同性。结果表明,由于体细胞克隆的变异,各继代植物的母本植物和组织培养再生植物之间发生了遗传变异。一些再生植物之间基因组大小的显着差异表明,组织培养期间植物遗传结构的变化也伴随着DNA的定量变化。然而,苹果砧木的遗传变异程度不同,所用的处理方式也不同。

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