Establishment of Start Codon Targeted Polymorphism Molecular Markers System and Genetic Diversity Analysis of Fritillaria thunbergii

IF 0.5 4区 医学
Yunzhe Dong, Qiuli Wu, Lili Dong, Huanru Guo, Zhonghua Wang
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Abstract

After years of selective breeding, numerous cultivars of Fritillaria thunbergii have been cultivated in various regions of Zhejiang Province, showing significant genomic and epigenetic differences. Molecular marker loci developed so far are mainly based on non-coding regions of the genome, and their identification efficiency is limited when applied to these cultivars. Therefore, this study used start codon targeted polymorphism molecular marker to detect PCR amplification of 100 Fritillaria thunbergii samples from various sources. The SCoT-PCR reaction system was optimized using a single-factor and orthogonal testing to determine the optimal conditions: DNA concentration of 4.2 ng • μL−1, primer concentration of 0.88 μmol • L−1, dNTP concentration of 0.35 mmol • L−1, Mg2+ concentration of 2.5 mmol • L−1, Supercharm Fidelity enzyme amount of 1.2 U, and total reaction volume of 25 μL. Moreover, 16 effective primers were identified, including SCoT1, SCoT2, SCoT3, SCoT7, SCoT11, SCoT12, SCoT14, SCoT17, SCoT19, SCoT23, SCoT25, SCoT26, SCoT29, SCoT35, and SCoT37. The annealing temperature for each primer was determined. Among them, SCoT14, SCoT25, SCoT29, SCoT35, and SCoT41 were specific for identifying six main cultivars: “Zhebei 1”, “Zhebei 2”, “Zhebei 3”, “Xuansanzi”, “Sanzi”, and “Duozi”. SCoT7, SCoT14, and SCoT35 were useful in tracking mutations in progeny of Zhebei 3 after radiation treatment, while SCoT29 could distinguish Zhebei 1 from Chunan. In addition, cluster analysis was conducted to simulate the genetic relationship between different cultivars, demonstrating that genetic similarity analysis is practically significant for predicting genetic correlation among different cultivars. The results not only improve the identification ability of Fritillaria thunbergii cultivars, but also help objectively evaluate their genetic stability and environmental adaptability. These achievements provide important scientific evidence for the ecological protection and utilization of germplasm resources of Fritillaria thunbergii and serve as a reference for exploring genetic diversity and evolution of traditional Chinese medicine.
建立起始密码子靶向多态性分子标记系统并分析蓟马的遗传多样性
经过多年的选育,浙江省各地培育出了大量的毛蕊花栽培品种,这些栽培品种在基因组和表观遗传方面表现出显著的差异。目前开发的分子标记位点主要基于基因组的非编码区,应用于这些栽培品种的鉴定效率有限。因此,本研究采用起始密码子定向多态性分子标记,对来自不同来源的 100 个蓟马样品进行 PCR 扩增检测。采用单因素和正交试验优化了 SCoT-PCR 反应系统,以确定最佳条件:DNA 浓度为 4.2 ng - μL-1,引物浓度为 0.88 μmol - L-1,dNTP 浓度为 0.35 mmol - L-1,Mg2+ 浓度为 2.5 mmol - L-1,Supercharm Fidelity 酶量为 1.2 U,总反应体积为 25 μL。此外,还确定了 16 种有效引物,包括 SCoT1、SCoT2、SCoT3、SCoT7、SCoT11、SCoT12、SCoT14、SCoT17、SCoT19、SCoT23、SCoT25、SCoT26、SCoT29、SCoT35 和 SCoT37。确定了每种引物的退火温度。其中,SCoT14、SCoT25、SCoT29、SCoT35 和 SCoT41 对鉴定 6 个主要栽培品种具有特异性:"浙贝 1 号"、"浙贝 2 号"、"浙贝 3 号"、"宣山子"、"桑子 "和 "朵子"。SCoT7、SCoT14和SCoT35有助于追踪 "浙北3号 "放射治疗后后代的突变情况,而SCoT29则可以区分 "浙北1号 "和 "浙南"。此外,还通过聚类分析模拟了不同栽培品种之间的遗传关系,证明遗传相似性分析对于预测不同栽培品种之间的遗传相关性具有实际意义。这些结果不仅提高了对蓟马栽培品种的鉴定能力,而且有助于客观评价其遗传稳定性和环境适应性。这些研究成果为中药材种质资源的生态保护和利用提供了重要的科学依据,也为探索中药材遗传多样性和进化提供了参考。
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来源期刊
Journal of Biobased Materials and Bioenergy
Journal of Biobased Materials and Bioenergy 工程技术-材料科学:生物材料
自引率
0.00%
发文量
60
审稿时长
6 months
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