A A Hussein Mohammed, Eid Manal, Rahimi Mehdi, Filimban Faten Zubair, Abd El-Moneim Diaa
Department of Botany (Genetic Branch), Faculty of Agriculture, Suez Canal University, Ismailia, Egypt.
Department of Biotechnology, Institute of Science and High Technology and Environmental Sciences, Graduate University of Advanced Technology, Kerman, Iran.
PeerJ. 2023 Sep 28;11:e15722. doi: 10.7717/peerj.15722. eCollection 2023.
Genetic improvement mainly depends on the level of genetic variability present in the population, and the degree of genetic diversity in a population largely determines the rate of genetic advancement. For analyzing genetic diversity and determining cultivar identities, a molecular marker is a useful tool. Using 30 SSR (simple sequence repeat) and 30 RAPD (randomly amplified polymorphic DNA) markers, this study evaluated the genetic divergence of 17 mango cultivars. The effectiveness of the two marker systems was evaluated using their genetic diversity characteristics. Additionally, the effects of SM (simple matching) and Dice similarity coefficients and their effects on mango clustering were evaluated. The findings showed that SSR markers generated 192 alleles, all of which were polymorphic (100%). With RAPD markers, 434 bands were obtained, 361 of which were polymorphic (83%). The average polymorphic information content (PIC) for RAPD and SSR was 0.378 and 0.735, respectively. Using SSR markers resulted in much higher values for other genetic diversity parameters compared to RAPD markers. Furthermore, grouping the genotypes according to the two similarity coefficients without detailed consideration of these coefficients could not influence the study results. The RAPD markers OPA_01, OPM_12 followed by OPO_12 and SSR markers MIAC_4, MIAC_5 followed by mMiCIR_21 were the most informative in terms of describing genetic variability among the cultivars under study; they can be used in further investigations such as genetic mapping or marker-assisted selection. Overall, 'Zebda' cultivar was the most diverse of the studied cultivars.
遗传改良主要取决于群体中存在的遗传变异水平,而群体中的遗传多样性程度在很大程度上决定了遗传进展的速度。对于分析遗传多样性和确定品种特性而言,分子标记是一种有用的工具。本研究使用30个SSR(简单序列重复)和30个RAPD(随机扩增多态性DNA)标记,评估了17个芒果品种的遗传差异。利用这两种标记系统的遗传多样性特征评估了它们的有效性。此外,还评估了简单匹配系数(SM)和戴斯相似系数及其对芒果聚类的影响。结果表明,SSR标记产生了192个等位基因,所有这些等位基因都是多态性的(100%)。使用RAPD标记获得了434条带,其中361条是多态性的(83%)。RAPD和SSR的平均多态信息含量(PIC)分别为0.378和0.735。与RAPD标记相比,使用SSR标记得出的其他遗传多样性参数值要高得多。此外,在没有详细考虑这些系数的情况下,根据这两种相似系数对基因型进行分组不会影响研究结果。就描述所研究品种间的遗传变异而言,RAPD标记OPA_01、OPM_12以及随后的OPO_12和SSR标记MIAC_4、MIAC_5以及随后的mMiCIR_21信息最为丰富;它们可用于进一步的研究,如遗传图谱绘制或标记辅助选择。总体而言,‘Zebda’品种是所研究品种中遗传多样性最高的。