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中国农学通报 ›› 2021, Vol. 37 ›› Issue (1): 61-66.doi: 10.11924/j.issn.1000-6850.casb20200100068

所属专题: 园艺

• 林学·园艺·园林 • 上一篇    下一篇

苹果SSR-PCR反应体系的建立与优化

刘琳1(), 孙晓帅2, 李乾1, 范书臣1, 时鸿迪1, 马钧3, 刘丹丹1()   

  1. 1云南大学农学院,昆明 650091
    2西藏大学理学院,拉萨 850000
    3云南省农业科学院园艺作物所,昆明 650091
  • 收稿日期:2020-01-20 修回日期:2020-03-24 出版日期:2021-01-05 发布日期:2020-12-25
  • 通讯作者: 刘丹丹
  • 作者简介:刘琳,女,1994年出生,陕西铜川人,硕士,研究方向为果树种质资源。通信地址:650091 云南省昆明市呈贡区 云南大学呈贡校区农学院,Tel:0871-65031539,E-mail:xuecangll@163.com
  • 基金资助:
    云南省科技计划“云南特色水果品质提升与优势品牌创建”(2019ZG002);国家自然科学基金“苹果砧木平邑甜茶PcG蛋白MhMSI1调控单性生殖的分子机理”(31660566)

Establishment and Optimization of SSR-PCR Reaction System of Apple Plants

Liu Lin1(), Sun Xiaoshuai2, Li Qian1, Fan Shuchen1, Shi Hongdi1, Ma Jun3, Liu Dandan1()   

  1. 1College of Agriculture, Yunnan University, Kunming 650091
    2College of Science, Tibet University, Lhasa 850000
    3Institute of Horticultural Crops, Yunnan Academy of Agricultural Sciences, Kunming 650091
  • Received:2020-01-20 Revised:2020-03-24 Online:2021-01-05 Published:2020-12-25
  • Contact: Liu Dandan

摘要:

为建立苹果属植物SSR-PCR反应优化体系,采用L16(45)正交实验和退火温度梯度实验,分析反应体系中使用的模板、引物、Mg2+、dNTPs以及Top Taq酶浓度对扩增产物的影响,并对这5个因素进行4个水平不同浓度梯度的筛选和优化。结果表明,引物浓度对SSR-PCR反应体系的影响最大,通过综合分析最终确定SSR-PCR的25 μL最佳反应体系为:30~60 ng DNA模板,1.2 μL正反向引物(5 μmol/L),0.5 μL dNTPs(2.5 mmol/L),0.5 μL Top Taq酶(2.5 U/μL)以及2.5 μL 10× Top Taq buffer(含Mg2+)。利用优化后的反应体系对蔷薇科苹果属的21种植物材料进行检测,实验结果表明扩增产物均在100~200 bp左右,可扩增出2~3个有效等位基因。通过优化反应体系中的各影响因素,建立了最佳的SSR-PCR反应体系,可为苹果属植物不同种群的遗传变异研究及亲缘关系的分子鉴定提供前期研究基础。

关键词: 苹果, SSR-PCR最佳反应体系, 正交设计试验, 种质资源, 单因素试验

Abstract:

To establish an optimal SSR-PCR system for apple plants, the L16(45) orthogonal test and the annealing temperature gradient experiment were used to analyze the effect of template concentration, primer concentration, Mg2+concentration, dNTPs concentration and Top Taq enzyme concentration in the SSR reaction system on the amplification products. Additionally, the above five factors were screened and optimized at 4 different levels. The results showed that the primer concentration factor had the greatest impact on the SSR-PCR reaction system. Though analysis, the optimal reaction system of 25 μL for SSR-PCR was finally determined to be as follows: 30-60 ng DNA template, 1.2 μL forward and reverse primer (5 μmol/L), 0.5 μL dNTPs (2.5 mmol/L), 0.5 μL Top Taq enzyme (2.5 U/μL) and 2.5 μL 10×Top Taq buffer (containing Mg2+). Finally, optimized reaction system was used for PCR amplification using 21 different apple plants, and the amplification products were about 100-200 bp displaying 2-3 alleles. The optimal SSR-PCR reaction system can provide a preliminary basis for the genetic variation research and molecular identification of genetic relationships in different populations of apple plants.

Key words: apple, SSR-PCR optimal reaction system, orthogonal design experiment, germplasm resource, single factor test

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