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首页> 外文期刊>African Journal of Biotechnology >Molecular characterization of ten mango cultivars using simple sequences repeat (SSR) markers
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Molecular characterization of ten mango cultivars using simple sequences repeat (SSR) markers

机译:使用简单重复序列(SSR)标记对十个芒果品种进行分子鉴定

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Simple sequence repeats (SSRs) which is an efficient genetic markers for comparative genome mapping can be helpful in the classification of genotypes, germplasm resource utilization and breeding programmes. Therefore, the present study was conducted to show genetic variation and investigate inter-relationship between ten mango genotypes. Twenty (20) SSR markers were tested with 10 genotypes: Kalepad, Neelum, Swarnarekha, Alphonso Rumani, Sendura, Banganapalli, Himayuddin, Mulgoa and Bangalora. The genomic DNA was extracted from the leaf samples using cetyltrimethyl ammonium bromide (CTAB) method. Polymerase chain reaction (PCR) amplification of the DNA isolated from 10 mango genotypes with 20 SSR primers produced a total of 240 amplified products, of which 184 were polymorphic and 56 monomorphic. The sizes of the alleles detected ranged from 120 to 369 bp. SSR markers were highly polymorphic with an average of 2.70 alleles per primers. SSRs gave moderate values of polymorphic information content (PIC) range of 0.320 to 0.774. The amplified products varied between 2 (LMMA 1, 5, 7, 12, 16, MiSHRS-1 and MiSHRS-37) to 3 and 4 (LMMA 4, 6, 9, 10, 11, 13, 14, 15 MiSHRS-4, 48, 18, 39 and LMMA 8) bands per primer. We obtained moderate degree of genetic diversity, with Jaccard’s similarity co-efficient values ranging from 0.075 between cluster I and II to 0.285 between clusters II and III. The dendrogram generated from the unweighted pair group arithmetic average (UPGMA) cluster analysis broadly placed 10 mango cultivars into three major clusters at co-efficient similarity of 0.65. The cluster size varied from 1 to 6 and cluster III was the largest cluster comprising of six cultivars followed by cluster II possessing three and cluster I possessing one variety. Cluster I had the highest diverse cultivars namely, Kalepad, Neelum and Swarnarekha. Cluster II included cultivar of Alphonso. Cluster III contain the cultivars viz., Rumani, Sendura, Bangnapalli, Himayuddin, Mulgoa and Bangalora. Unique fingerprints were identified in the cultivars. The unique fingerprints size ranged from LMMA-8 (257-270 bp), LMMA-11 (232- 245 bp) to MiSHRS 39 (340-369 bp). The tendency of clustering among mango cultivars revealed that they have strong affinity towards further breeding programme.
机译:简单序列重复(SSR)是比较基因组作图的有效遗传标记,可有助于基因型的分类,种质资源利用和育种计划。因此,本研究旨在显示遗传变异并研究十个芒果基因型之间的相互关系。用十个基因型测试了二十(20)个SSR标记:Kalepad,Neelum,Swarnarekha,Alphonso Rumani,Sendura,Banganapalli,Himayuddin,Mulgoa和Bangalora。使用十六烷基三甲基溴化铵(CTAB)方法从叶片样品中提取基因组DNA。用20个SSR引物对10个芒果基因型分离的DNA进行聚合酶链反应(PCR)扩增,共产生240个扩增产物,其中184个为多态性,56个为单态性。检测到的等位基因的大小在120至369 bp之间。 SSR标记高度多态,每个引物平均有2.70个等位基因。 SSR给出的多态信息含量(PIC)范围介于0.320至0.774之间。扩增产物在2(LMMA 1、5、7、12、16,MiSHRS-1和MiSHRS-37)至3和4(LMMA 4、6、9、10、11、13、14、15 MiSHRS-4)之间变化每个引物具有48、18、39和LMMA 8)条带。我们获得了中等程度的遗传多样性,Jaccard的相似系数值介于I类和II类之间的0.075到II类和III类之间的0.285。通过非加权对算术平均值(UPGMA)聚类分析生成的树状图将10个芒果品种广泛地分为三个主要聚类,其系数相似度为0.65。簇的大小从1到6不等,簇III是由六个品种组成的最大的簇,其次是具有三个品种的簇II和具有一个品种的簇I。第一类品种具有最高的品种,即甘蓝菜,Neelum和Swarnarekha。第二类包括阿方索的品种。第III组包含Rumani,Sendura,Bangnapalli,Himayuddin,Mulgoa和Bangalora的品种。在品种中鉴定出独特的指纹。独特的指纹大小范围从LMMA-8(257-270 bp),LMMA-11(232-245 bp)到MiSHRS 39(340-369 bp)。芒果品种之间的聚集趋势表明,它们对进一步的育种计划具有很强的亲和力。

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