Aradhya Mallikarjuna K, Stover Ed, Velasco Dianne, Koehmstedt Anne
National Clonal Germplasm Repository, USDA-ARS, University of California, Davis, One Shields Avenue, Davis, CA, 95616, USA.
Genetica. 2010 Jun;138(6):681-94. doi: 10.1007/s10709-010-9442-3. Epub 2010 Mar 10.
One hundred ninety-four germplasm accessions of fig representing the four fig types, Common, Smyrna, San Pedro, and Caprifig were analyzed for genetic diversity, structure, and differentiation using genetic polymorphism at 15 microsatellite loci. The collection showed considerable polymorphism with observed number of alleles per locus ranging from four for five different loci, MFC4, LMFC14, LMFC22, LMFC31 and LMFC35 to nine for LMFC30 with an average of 4.9 alleles per locus. Seven of the 15 loci included in the genetic structure analyses exhibited significant deviation from panmixia, of which two showed excess and five showed deficiency of heterozygote. The cluster analysis (CA) revealed ten groups with 32 instances of synonymy among cultivars and groups differed significantly for frequency and composition of alleles for different loci. The principal components analysis (PCA) confirmed the results of CA with some groups more differentiated than the others. Further, the model based Bayesian approach clustering suggested a subtle population structure with mixed ancestry for most figs. The gene diversity analysis indicated that much of the total variation is found within groups (H (G) /H (T) = 0.853; 85.3%) and the among groups within total component (G (GT) = 0.147) accounted for the remaining 14.7%, of which approximately 64% accounted for among groups within clusters (G (GC) = 0.094) and approximately 36% among clusters (G (CT) = 0.053). The analysis of molecular variance (AMOVA) showed approximately similar results with nearly 87% of variation within groups and approximately 10% among groups within clusters, and approximately 3% among clusters. Overall, the gene pool of cultivated fig analyzed possesses substantial genetic polymorphism but exhibits narrow differentiation. It is evident that fig accessions from Turkmenistan are somewhat genetically different from the rest of the Mediterranean and the Caucasus figs. The long history of domestication and cultivation with widespread dispersal of cultivars with many synonyms has resulted in a great deal of confusion in the identification and classification of cultivars in fig.
利用15个微卫星位点的遗传多态性,对代表普通型、斯密尔那型、圣佩德罗型和野生型这四种无花果类型的194份无花果种质资源进行了遗传多样性、结构和分化分析。该收集品显示出相当大的多态性,每个位点观察到的等位基因数从五个不同位点(MFC4、LMFC14、LMFC22、LMFC31和LMFC35)的4个到LMFC30的9个不等,平均每个位点有4.9个等位基因。遗传结构分析中包含的15个位点中有7个显示出与随机交配的显著偏差,其中2个显示杂合子过剩,5个显示杂合子不足。聚类分析(CA)揭示了10个组,品种间有32个同义实例,不同组在不同位点的等位基因频率和组成上有显著差异。主成分分析(PCA)证实了CA的结果,一些组比其他组更具分化性。此外,基于模型的贝叶斯方法聚类表明,大多数无花果具有微妙的种群结构和混合血统。基因多样性分析表明,大部分总变异存在于组内(H(G)/H(T)=0.853;85.3%),组内成分间(G(GT)=0.147)占其余14.7%,其中约64%占聚类内组间(G(GC)=0.094),约36%占聚类间(G(CT)=0.053)。分子方差分析(AMOVA)显示了大致相似的结果,组内变异近87%,聚类内组间变异约10%,聚类间变异约3%。总体而言,所分析的栽培无花果基因库具有大量的遗传多态性,但分化程度较窄。显然,来自土库曼斯坦的无花果种质在遗传上与地中海其他地区和高加索地区的无花果有所不同。长期的驯化和栽培历史,以及具有许多同义词的品种的广泛传播,导致了无花果品种鉴定和分类的大量混乱。