Genetic Diversity of Some Sweet Cherry Cultivars Based on Molecular Markers

I. Berindean, E. Tămaş, Oana Maria Toderic, I. Zagrai
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Abstract

Sweet cherry ( Prunus avium L.), originated around the Caspian and Black Sea, is an important fruit tree species of economic interest, and hence, breeding and conservation are requested (. Genetic analysis at the molecular level can be used effectively to study molecular polymorphism existing between intraspecific and interspecific tree species and phylogenetic relationships between them and their hybrids. The purpose of this study was to characterize and determine genetic relationships among the sweet cherry native genotypes belonging to Fruit Research & Development Station Bistrita, Romania, using RAPD markers. To eliminate the existence of possible synonyms from national romanian collection, we collect four Van cultivars, from four different national collection. For molecular analysis of the 16 varieties of sweet cherry were considered 13 RAPD primers selected from the literature. They were later used to determine the genetic variability at the molecular level using PAST program, and the dendrogram was generated based on Jaccard’s genetic distance. The dendrogram constructed by PAST software. The quantity and quality of the DNA obtained was suitable to achieve PCR amplification step. Only seven out of the 13 RAPD primers have generate polymorphic bands. The rest of seven were monomorphics. The most polymorphic primer was OPB10 which generated 11 bands from which 100% were polymorphic.Seven RAPD primers generated a high level of polymorphism which allowed to divide these cherry varieties into two groups according to their genetic geographical origin and the pedigree.
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基于分子标记的甜樱桃品种遗传多样性研究
甜樱桃(Prunus avium L.)原产于里海和黑海沿岸,是一种重要的经济树种,因此需要进行育种和保护。分子水平的遗传分析可以有效地研究树种种内和种间的分子多态性及其与杂交种的系统发育关系。本研究旨在利用RAPD标记对罗马尼亚Bistrita果树研究站的甜樱桃本地基因型进行遗传关系分析。为了消除罗马尼亚国家收藏中可能存在的同义词,我们从四个不同的国家收藏中收集了四个Van品种。本文从文献中选取13条RAPD引物对16个甜樱桃品种进行分子分析。然后利用PAST程序在分子水平上确定遗传变异,并根据Jaccard遗传距离生成树突图。用PAST软件构建树形图。所获得的DNA数量和质量适合进行PCR扩增步骤。13条RAPD引物中只有7条产生多态性条带。剩下的七个是单态的。多态性最高的引物为OPB10,共产生11条条带,多态性率为100%。7条RAPD引物产生了高水平的多态性,使这些樱桃品种可以根据其遗传地理来源和家系划分为两类。
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