首页> 外文期刊>International Journal of Forestry Research >Clonal Identification Based on Quantitative, Codominant, and Dominant Marker Data: A Comparative Analysis of Selected Willow (SalixL.) Clones
【24h】

Clonal Identification Based on Quantitative, Codominant, and Dominant Marker Data: A Comparative Analysis of Selected Willow (SalixL.) Clones

机译:基于定量,显性和显性标记数据的克隆鉴定:柳柳克隆的比较分析

获取原文
       

摘要

Clonal identification in forestry may employ different means, each with unique advantages. A comparative evaluation of different approaches is reported. Nine quantitative leaf morphometric parameters, 15 variable codominant (isoenzyme) and 15 variable dominant (RAPD) loci, were used. All clones presented unique multilocus isoenzyme genotypes and 86% presented unique multilocus RAPD genotypes. Quantitative, isoenzyme and molecular data were subjected to principal component analysis, the latter two data sets after vector transformation. Most of the variability (quantitative 99%, isoenzyme 72.5%, RAPD 89%) was accounted for in the first three axes. This study has shown: (1) individual quantitative parameters were inefficient for clonal identification, (2) multilocus clonal identification was successful, (3) dominant markers were more polymorphic than codominant ones: 1.5 variable loci per enzyme system, 7.5 variable RAPD loci per primer, (4) 15 codominant marker loci could identify about 2.8 times more individuals than 15 dominant ones, but this advantage is surpassed when 42 dominant loci are employed, (5) multivariate analysis of morphological, codominant and dominant genetic data could not discriminate at the clonal level. It was concluded that due to their higher number of loci available dominant markers perform better than codominant ones, despite the higher informativeness of the latter.
机译:林业中的克隆鉴定可以采用不同的方法,每种方法都有其独特的优势。报告了对不同方法的比较评估。使用了9个定量叶片形态参数,分别有15个可变优势基因(同工酶)和15个可变优势基因(RAPD)基因座。所有克隆均表现出独特的多基因座同工酶基因型,86%呈现独特的多基因座RAPD基因型。对定量,同工酶和分子数据进行主成分分析,后两个数据集经过载体转化。大部分变异性(定量99%,同工酶72.5%,RAPD 89%)在前三个轴中得到解释。这项研究表明:(1)个体定量参数对克隆鉴定无效,(2)多位点克隆鉴定成功,(3)显性标记比共显性标记具有更多的多态性:每个酶系统1.5个可变基因座,每个酶系统7.5个可变RAPD基因座引物,(4)15个显性标记基因座比15个显性标记物能鉴定出大约2.8倍的个体,但是当使用42个显性基因座时,这一优势被超越。(5)形态,显性和显性遗传数据的多变量分析无法区分克隆级别。得出的结论是,尽管它们的信息量较高,但由于它们的基因座数量更多,可利用的显性标记的性能要优于共显性标记。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号