本研究由国家公益性行业(农业)专项(201103005);福建省省长基金项目(Sbxd0903);福建省财政专项“福建省农业科学科技创新团队建设基金”(STIF_Y01)专项经费资助。
国家公益性行业专项“绿肥作物生产与利用技术集成研究及示范”(200803029);福建省财政专项“福建省农业科学技术创新团队建设基金”(STIF—Y01)
以紫云英为研究材料,用哥伦比亚大学(UBC)公布的100条 ISSR引物和十一种紫云英品种的DNA为模板进行PCR扩增,筛选出33条扩增条带较好的ISSR引物 ,对其中的ISSR引物进行梯度PCR筛选出最佳的退火温度。再采用正交实验和单因素实验相结合的方法对紫云英ISSR-PCR反应体系的五种因素(模板,Mg2 , Taq DNA聚合酶,dNTP及引物)进行优化浓度。确立了适合紫云英的ISSR分析的反应体系。在25μL反应体系中,反应体系的量为:DNA模板50.00ng,Mg2 2.00mmol/L ,Taq聚合酶1.0 U,dNTP 0.25 mmol/L;引物0.20μmol/L ,2.5μL10譩uffer。本实验为以后利用ISSR 技术进行紫云英遗传多样性分析和物种保护奠定了技术基础;为开发紫云英SSR引物提供了条件。
The factors that affccting the ISSR(inter-simple sequence repeat)result of Astragalus sinicus.L. We studied and selected 33 ISSR primers which can amplify bands from the DNA of Astragalus sinicus.L.and the 33 ISSR primers all from the ISSR primers published by Columbia University. Bysetting the temperature gradient,the available primers’best annealing temperature are explored.The effect of the five main reaction elements(Mg2 、 TaqDNApolymerase、dNTP、 template and primer)on ISSR-PCR were all optimized by combining single factor experiments and othogonal test methed .then we establish the best ISSR-PCRreaction system.The best ISSR-PCR reaction system of Astragalus sinicus. is 25μl reaction system containting the DNA template 50.00ng,Mg2 concentration 2.00mmol/L,Taq enzyme dosageis 1.0U,dNTPs concention is 0.25mmol/L,primers0.20μmol/L, 2.5μL 10譩uffer. The seleted ISSR primers and annealing temperature is widespread and representative in Astragalus sinicusISSR-PCRmarker research and the result could provide the basis for the analysis of diversity , protection ;exploitation of SSR primers of Astragalus sinicus.
孙清信,陈 坚,张 辉,等.紫云英ISSR引物的筛选及PCR反应体系的优化[J].植物遗传资源学报,2012,13(5):870-878.
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