Fluch Silvia, Burg Agnes, Kopecky Dieter, Homolka Andreas, Spiess Nadine, Vendramin Giovanni G
AIT Austrian Institute of Technology GmbH, Health & Environment Department, Bioresources, 3430 Tulln, Austria.
BMC Res Notes. 2011 Oct 12;4:401. doi: 10.1186/1756-0500-4-401.
Norway spruce is widely distributed across Europe and the predominant tree of the Alpine region. Fast growth and the fact that timber can be harvested cost-effectively in relatively young populations define its status as one of the economically most important tree species of Northern Europe. In this study, EST derived simple sequence repeat (SSR) markers were developed for the assessment of putative functional diversity in Austrian Norway spruce stands.
SSR sequences were identified by analyzing 14,022 publicly available EST sequences. Tri-nucleotide repeat motifs were most abundant in the data set followed by penta- and hexa-nucleotide repeats. Specific primer pairs were designed for sixty loci. Among these, 27 displayed polymorphism in a testing population of 16 P. abies individuals sampled across Austria and in an additional screening population of 96 P. abies individuals from two geographically distinct Austrian populations. Allele numbers per locus ranged from two to 17 with observed heterozygosity ranging from 0.075 to 0.99.
We have characterized variable EST SSR markers for Norway spruce detected in expressed genes. Due to their moderate to high degree of variability in the two tested screening populations, these newly developed SSR markers are well suited for the analysis of stress related functional variation present in Norway spruce populations.
欧洲云杉广泛分布于欧洲,是阿尔卑斯地区的主要树种。其生长迅速,且在相对年轻的种群中就能经济高效地采伐木材,这使其成为北欧经济上最重要的树种之一。在本研究中,开发了基于EST的简单序列重复(SSR)标记,用于评估奥地利欧洲云杉林分中假定的功能多样性。
通过分析14,022条公开的EST序列鉴定出SSR序列。三核苷酸重复基序在数据集中最为丰富,其次是五核苷酸和六核苷酸重复。为60个位点设计了特异性引物对。其中,27个在从奥地利各地采集的16个欧洲云杉个体的测试群体以及来自奥地利两个地理上不同种群的另外96个欧洲云杉个体的筛选群体中表现出多态性。每个位点的等位基因数从2到17不等,观察到的杂合度从0.075到0.99不等。
我们对在表达基因中检测到的欧洲云杉可变EST SSR标记进行了表征。由于这些新开发的SSR标记在两个测试筛选群体中具有中度到高度的变异性,因此非常适合分析欧洲云杉种群中存在的与胁迫相关的功能变异。