海南龙血树RAPD-PCR反应体系的优化  

Optimization of RAPD-PCR reaction system for Dracaena cambodiana

作　　者：郑道君[1] 谢良商[1] 张文[1] 张治礼[1] 

机构地区：[1]海南省农业科学院农作物遗传育种重点实验室,海口571100

出　　处：《广西植物》2011年第1期31-35,86,共6页Guihaia

基　　金：国家自然科学基金(30760015);海南省自然科学基金(30831)~~

摘　　要：采用单因子试验和正交试验设计,对影响海南龙血树RAPD-PCR反应的模板DNA量、Mg2+、dNTP和引物浓度,Taq聚合酶用量等因子进行研究,分析各因子对RAPD-PCR扩增结果的影响,确立了海南龙血树RAPD-PCR反应的最佳条件,即在25μL反应体系中,包含10×buffer2.5μL,2.0mmol/L MgCl2,300μmol/L dNTPs,Taq酶1.5U,引物0.8μmol/L和DNA模板20ng。以此条件为基础,筛选出适用于海南龙血树RAPD-PCR分析的18条有效引物,为采用RAPD技术分析海南龙血树种群遗传变异水平和遗传结构打下了基础。Both single factor test and orthogonal design were applied to study the effects of main factors on the RAPD-PCR system for Dracaena cambodiana,in which the main factors included the content of template DNA,the concentration of Mg2＋、dNTPs and primers and the content of Taq DNA polymerase,and an optimal 25μL RAPD-PCR reaction system for D.cambodiana was established,including 2.5 μL 10×PCR buffer,2.0 mmol/L MgCl_2,300 μmol/L dNTPs,1.5 U Taq polymerase,0.8 μmol/L primers,and 20 ng DNA template.18 primers were selected for RAPD-PCR analysis for D.cambodiana using the optimized amplification system above,which can be employed for the analysis of genetic variation and structure of D.cambodiana population.

关 键 词：海南龙血树 RAPD 反应条件优化 有效引物筛选 

分 类 号：Q943[生物学—植物学]