Detection of in silico SSR Markers Specific to Uzun and Kırmızı Cultivars in Pistachio

Harun Karcı
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Abstract

In the current paper, it was aimed to detect the SSR markers that can be used in the prevention of confusion that may occur in breeding or nurseries, and directly genetically separating Uzun and Kırmızı pistachio cultivars from other commercial cultivars. A total of genotypes of 16 Pistacia vera species, one P. atlantica, one P. eurycarpa and two P. terebinthus species were obtained from the farmer's orchard in Nizip district of Gaziantep province for genetic characterization. Genetic diversity and clustering analyzes were performed with UPGMA (Unweighted Pair Group Method with Arithmetic Average) and STRUCTURE 2.3.4 programs using the scored SSR loci. Genetic relationship and population structure of genotypes were defined using common and distinct polymorphic PCR fragments. Cultivar-specific markers to be used in identifying and distinguishing the genetic structure of Uzun and Kırmızı cultivars were carried out in the current research. CUPOhBa2127 marker has the highest allele number (Na=10). In addition, 11 out of 25 SSR markers were explained as cultivar-specific SSRs that can distinguish Uzun and Kırmızı cultivars. These markers can be used directly by breeders and geneticists without any preliminary screnning of the markers. A quite serious providence will be achieved in the cost and time that will occur with the preliminary analysis, and thus, the confusion that may occur in large scale orchard establishments or nurseries will be reduced to pretty low levels with DNA analysis.
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开心果Uzun和Kırmızı品种特异SSR标记的检测
本论文的目的是寻找能够防止在育种或苗种中出现混淆的SSR标记,并将Uzun和Kırmızı开心果品种与其他商品品种直接进行遗传分离。从加济安泰普省尼齐普区农民果园中获得了16种黄连木、1种大西洋黄连木、1种eurycarpa和2种terebinthus的基因型,并进行了遗传鉴定。采用UPGMA (Unweighted Pair Group Method with Arithmetic Average)和STRUCTURE 2.3.4程序对SSR标记进行遗传多样性和聚类分析。利用常见和独特多态性PCR片段确定了基因型的亲缘关系和群体结构。本研究开展了用于乌尊和Kırmızı品种遗传结构鉴定和区分的品种特异性标记。CUPOhBa2127等位基因数量最多(Na=10)。此外,25个SSR标记中有11个被解释为品种特异性SSR,可以区分Uzun和Kırmızı品种。这些标记可以直接由育种家和遗传学家使用,而无需对标记进行任何初步筛选。初步分析将在成本和时间上实现相当认真的护理,因此,在大型果园机构或苗圃中可能出现的混乱将通过DNA分析减少到相当低的水平。
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