%0 Journal Article %T 甜樱桃栽培种指纹图谱构建及遗传多样性分析<br>Establishment of DNA Fingerprinting and Analysis of Genetic Diversity among Prunus aviun Cultivars %A 王丹丹 %A 付化瑞 %A 张彦文 %J 西北农业学报 %D 2017 %R 10.7606/j.issn.1004-1389.2017.12.010 %X 为了对甜樱桃品种进行分子鉴别及分析不同品种间的亲缘关系,以叶片直接进行PCR扩增,采用EST-SSR分子标记技术构建生产上常用的40个甜樱桃栽培品种的数字指纹图谱和模式指纹图谱数据库(Cluster Project)并进行遗传多样性分析。采用24对甜樱桃核心引物对所有品种基因组进行扩增,共检测到129个等位位点,包括118个多态性位点,多态性比率为91.2%。每对引物扩增出的等位位点数3~10个,每对引物平均扩增5.38个基因型,扩增条带大小介于100~500 bp,多态信息含量(PIC)为0.654,基因流(Nm)为1.402,平均杂合率为0.495。8对引物,即PA17、PA32、PA51、PA54、PA73、PA99、PA101和PA202可作为指纹图谱构建的首选引物,利用其中的PA17、PA51、PA99、PA101和PA202以引物组合方式构建指纹图谱可区分40个品种;聚类分析表明在遗传距离0.71处40个品种被分为5类,聚类结果与品种的特性及成熟期具有较高的一致性。<br>In order to identify the cultivars of Prunus aviun and analyze the genetic relationship among different cultivars at a molecular level, we constructed the digital fingerprint and model fingerprint(ClusterProject)for 40 common Prunus aviun cultivars using EST-SSR(Expressed Sequence Tag-Simple Sequence Repeats) molecular markers. The 24 pairs of primers amplified a total of 129 alleles including 118 polymorphic alleles with a polymorphism rate of 91.2%. Each pairs of primers can amplify 3-10 alleles, with an average of 5.38 alleles per locus. The length of amplified products was 100-500 bp, with the mean value of PIC(Polymorphism information content) being 0.654,Nm(Gene flow) being 1.402, and the mean value of Ho(Heterozygosity) being 0.495. Among the 24 primers, 8 primers can be used as a preferred choice for fingerprinting, namely PA17, PA32, PA51, PA54,PA73, PA99,PA101 and PA202, in which 5 primers(PA17, PA51, PA99, PA101 and PA202) can be employed in combination to identify the 40 cultivars. Cluster analysis showed that the 40 cultivars can be divided into five groups at a genetic distance of 0.71; the genetic relationship as indicated by the cluster completely reflected the characteristics and the maturation stage of the cultivars. %K 甜樱桃 EST-SSR标记 指纹图谱 遗传多样性 聚类分析< %K br> %K Prunus aviun EST-SSR markers Fingerprinting Genetic diversity Cluster analysis %U http://xbnyxb.alljournals.cn/ch/reader/view_abstract.aspx?file_no=20171210&flag=1