Parthiban S, Govindaraj P, Senthilkumar S
Division of Crop Improvement, ICAR- Sugarcane, Breeding Institute, Coimbatore, 641 007 Tamil Nadu India.
3 Biotech. 2018 Mar;8(3):144. doi: 10.1007/s13205-018-1172-8. Epub 2018 Feb 21.
Twenty-five primer pairs developed from genomic simple sequence repeats (SSR) were compared with 25 expressed sequence tags (EST) SSRs to evaluate the efficiency of these two sets of primers using 59 sugarcane genetic stocks. The mean polymorphism information content (PIC) of genomic SSR was higher (0.72) compared to the PIC value recorded by EST-SSR marker (0.62). The relatively low level of polymorphism in EST-SSR markers may be due to the location of these markers in more conserved and expressed sequences compared to genomic sequences which are spread throughout the genome. Dendrogram based on the genomic SSR and EST-SSR marker data showed differences in grouping of genotypes. A total of 59 sugarcane accessions were grouped into 6 and 4 clusters using genomic SSR and EST-SSR, respectively. The highly efficient genomic SSR could subcluster the genotypes of some of the clusters formed by EST-SSR markers. The difference in dendrogram observed was probably due to the variation in number of markers produced by genomic SSR and EST-SSR and different portion of genome amplified by both the markers. The combined dendrogram (genomic SSR and EST-SSR) more clearly showed the genetic relationship among the sugarcane genotypes by forming four clusters. The mean genetic similarity (GS) value obtained using EST-SSR among 59 sugarcane accessions was 0.70, whereas the mean GS obtained using genomic SSR was 0.63. Although relatively lower level of polymorphism was displayed by the EST-SSR markers, genetic diversity shown by the EST-SSR was found to be promising as they were functional marker. High level of PIC and low genetic similarity values of genomic SSR may be more useful in DNA fingerprinting, selection of true hybrids, identification of variety specific markers and genetic diversity analysis. Identification of diverse parents based on cluster analysis can be effectively done with EST-SSR as the genetic similarity estimates are based on functional attributes related to morphological/agronomical traits.
将从基因组简单序列重复(SSR)开发的25对引物与25个表达序列标签(EST)SSR进行比较,以使用59份甘蔗遗传材料评估这两组引物的效率。与EST-SSR标记记录的PIC值(0.62)相比,基因组SSR的平均多态性信息含量(PIC)更高(0.72)。EST-SSR标记中相对较低的多态性水平可能是由于这些标记位于比遍布整个基因组的基因组序列更保守和表达的序列中。基于基因组SSR和EST-SSR标记数据的聚类图显示了基因型分组的差异。使用基因组SSR和EST-SSR分别将总共59份甘蔗种质分为6个和4个簇。高效的基因组SSR可以对由EST-SSR标记形成的一些簇的基因型进行亚聚类。观察到的聚类图差异可能是由于基因组SSR和EST-SSR产生的标记数量不同以及两种标记扩增的基因组不同部分所致。组合聚类图(基因组SSR和EST-SSR)通过形成四个簇更清楚地显示了甘蔗基因型之间的遗传关系。在59份甘蔗种质中使用EST-SSR获得的平均遗传相似性(GS)值为0.70,而使用基因组SSR获得的平均GS为0.63。尽管EST-SSR标记显示的多态性水平相对较低,但由于它们是功能标记,发现EST-SSR显示的遗传多样性很有前景。基因组SSR的高PIC水平和低遗传相似性值可能在DNA指纹识别、真杂种选择、品种特异性标记鉴定和遗传多样性分析中更有用。基于聚类分析鉴定不同的亲本可以有效地使用EST-SSR进行,因为遗传相似性估计基于与形态/农艺性状相关的功能属性。