油菜纯合子系遗传多样性的分子评价

M. A. El-Aziz, R. Habiba
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引用次数: 9

摘要

为了评估油菜10个纯合子系的遗传多样性,8个RAPD引物和5个ISSR引物以及2个Triple-RAPD的不同组合成功地产生了可重复和可靠的扩增子。利用所有分子标记技术共扩增出115个扩增子,其中多态性扩增59个(51.3%),独特扩增21个(18.3%)。ISSR技术在平均分辨率Rp(13.6)和标记扩增数/PCR反应数(1.8)方面表现最好。在所有ISSR目标微卫星中,重复基序(GA)n在其他ISSR引物所瞄准的重复基序中频率更高。所有分子标记技术与组合数据的分子距离均呈极显著正相关,表明组合数据的分子距离在准确评价油菜纯合子系遗传多样性和鉴定遗传亲缘关系方面是可靠的。因此,采用聚类分析和主坐标(PCo)分析表明,所研究的纯合子系之间的相似度较高。此外,PCo分析成功地将这些品系划分为4个类群,表明PCo分析成功地评估了所研究品系的遗传多样性和异质性。另一方面,对油菜纯合子系的遗传指纹图谱进行DNA-Profile图分析,结果表明,每个纯合子系的扩增子相互分化,平均扩增子数为93.3个,分子标记数量多样,表明DNA-Profile也是分子鉴定的有效工具。在此基础上,这些技术具有鉴定油菜纯合子系特异性标记的潜力,这表明这些标记可以作为油菜育种和改良的可靠资源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
MOLECULAR ASSESSMENT OF GENETIC DIVERSITY IN SOME CANOLA HOMOZYGOUS LINES
In order to assess genetic diversity among ten homozygous lines of Canola, eight RAPD and five ISSR primers as well as two various combinations of Triple-RAPD were successful in generating reproducible and reliable amplicons. A total of 115 amplicons were amplified using all molecular marker techniques applied in this study, 59 (51.3%) of them were polymorphic of which 21 (18.3%) were unique markers. ISSR technique was the best in terms of the average resolving power Rp (13.6) and number of marker amplicons/PCR reaction (1.8). From all of the targeted microsatellites by ISSRs, the repetitive motif (GA)n was more frequent from all repetitive motifs targeted by the other ISSR primers. Highly significant positive correlations were found for molecular distance among all of these molecular marker techniques and combined data, which indicates the reliability of the combined data for molecular distances in accurate assessment for genetic diversity and identifying the genetic relationships between all studied homozygous lines in canola. Accordingly, Cluster analysis and Principal Coordinate (PCo) analysis based on combined data were used for indicating degree of similarity which was high between all the studied homozygous lines. Moreover, PCo analysis have managed to divide these lines into four groups indicating that PCo analysis was succeeded in assessment of genetic diversity and description of heterogeneity within studied lines. On the other hand, the genetic fingerprint for all homozygous lines of canola was performed as DNA-Profile diagram, showing that the amplicons per homozygous line were differentiated for each other with average of 93.3 amplicons and with an appropriate number of diverse molecular markers, indicating that DNA-Profile also is a useful tool for molecular identification. Based on that, these techniques have the potential to identify specific markers for homozygous lines of canola, which indicates the possibility of using these markers as reliable resources for breeding and improvement of canola.
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