ZHAO Wanyue,LENG Qiusi,XIONG Jian,et al.Establishment and Optimization of ISSR-PCR Reaction System for Meconopsis integrifolia[J].Northern Horticulture,2018,42(14):80-86.[doi:10.11937/bfyy.20174097]
全缘叶绿绒蒿ISSR体系的建立与优化
- Title:
- Establishment and Optimization of ISSR-PCR Reaction System for Meconopsis integrifolia
- 文献标志码:
- A
- 摘要:
- 以全缘叶绿绒蒿的DNA为模板,利用正交实验设计,研究了Mg2+、dNTPs、引物、Taq DNA聚合酶、DNA这5种PCR反应成分对反应体系的影响,以期建立并优化一个适合全缘叶绿绒蒿的ISSR反应体系,并用优化的体系对UBC公布的100条ISSR引物进行筛选。结果表明:在50 μL优化后的反应体系中,含3 mmol·L-1 Mg2+、2 mmol·L-1 dNTPs、0.4 mmol·L-1引物、1.25 U Taq DNA聚合酶、60 ng DNA。通过梯度PCR仪检验,确定了适宜的退火温度、延伸时间和循环次数。利用该体系共筛选出16条ISSR引物,并对全缘叶绿绒蒿共10株个体材料进行扩增检验,获得了较好的扩增效果。利用该体系,可为今后ISSR标记在绿绒蒿属植物的种质鉴定和遗传多样性分析等方面的应用提供一定的试验基础。
- Abstract:
- The M.integrifolia was used as template in this study.And the effects of five PCR reaction components including Mg2+,dNTPs,primers,Taq DNA polymerase,and DNA on the reaction system were studied by using the orthogonal design.The purpose was establishment and optimization of ISSR-PCR reaction system for M.integrifolia,and screened 100 ISSR primers published by UBC with this system.The results showed that the 50 μL reaction system,including 3 mmol·L-1 Mg2+,2 mmol·L-1 dNTPs,0.4 mmol·L-1 primers,1.25 U Taq DNA polymerase,60 ng DNA.And the suitable annealing temperature,extension time and cycle times were determined by gradient PCR.A total of 16 ISSR primers were screened by the system,and 10 individual materials were tested for amplification,which obtained good amplification results.This system could provide some experimental basis for the future study on germplasm identification and genetic diversity analysis of M.Vig.by using ISSR marker.
相似文献/References:
[1]肖志娟,翟梅枝,许静,等.不同核桃品种的ISSR标记分析[J].北方园艺,2013,37(04):103.
[2]刘志曦,李志强,魏海莲,等.平菇ISSR遗传多样性分析[J].北方园艺,2014,38(12):94.
LIU Zhi-xi,LI Zhi-qiang,WEI Hai-lian,et al. Phylogenetic Analysis of Oyster Mushrooms by ISSR Marker[J].Northern Horticulture,2014,38(14):94.
[3]李 娜,张存旭,崔晓燕,等.栓皮栎ISSR反应体系的建立[J].北方园艺,2014,38(13):93.
LI Na,ZHANG Cun-xu,CUI Xiao-yan,et al.Establishment of ISSR Reaction System in Quercus variabilis [J].Northern Horticulture,2014,38(14):93.
[4]王鸿磊,丁 强,吕 蔚,等.我国双孢菇菌株与国外引进菌株间亲缘关系的ISSR分析[J].北方园艺,2014,38(11):96.
WANG Hong-lei,DING qiang,LV Wei,et al.Genetic Relationship Based on ISSR Markers Among Agaricus bisporus Strains From China and Overseas[J].Northern Horticulture,2014,38(14):96.
[5]李 娜,张存旭,刘 伟,等.毛梾ISSR-PCR反应体系的建立[J].北方园艺,2013,37(22):114.
LI Na,ZHANG Cun-xu,LIU Wei,et al.Establishment of ISSRPCR Reaction System of Cornus walteri[J].Northern Horticulture,2013,37(14):114.
[6]黄萌,陈尚钘,杨光耀,等.古樟ISSR扩增条件的优化[J].北方园艺,2013,37(07):116.
HUANG Meng,CHEN Shang-xing,YANG Guang-yao,et al.Optimization of ISSR Amplification Conditions in Ancient Camphor-trees[J].Northern Horticulture,2013,37(14):116.
[7]吴春燕,高义,宋廷宇,等.正交设计优化大白菜ISSR-PCR 反应体系[J].北方园艺,2012,36(05):127.
WU Chun-yan,GAO Yi,SONG Ting-yu,et al.Optimization of an ISSR-PCR Reaction System of Chinese Cabbage by Orthogonal Design[J].Northern Horticulture,2012,36(14):127.
[8]陈名红,李 玉,刘 多,等.适于ISSR-PCR扩增的百合基因组DNA的提取[J].北方园艺,2012,36(24):108.
CHEN Ming-hong,LI Yu,LIU Duo,et al.Extraction of Genomic DNA for ISSR-PCR Reaction in Lilium[J].Northern Horticulture,2012,36(14):108.
[9]张运峰,胡芬.红掌组培再生植株中表型突变体的ISSR分析[J].北方园艺,2014,38(21):101.
ZHANG Yun-feng,HU Fen.ISSR Analysis of Phenotypic Variants in Tissue Culturing Regeneration Plants of Anthurium andraeanum[J].Northern Horticulture,2014,38(14):101.
[10]孙叶迎,陈丽飞,刘树英,等.长白山区杓兰属植物ISSR-PCR最佳反应体系的建立[J].北方园艺,2013,37(24):92.
SUN Ye-ying,CHEN Li-fei,LIU Shu-ying,et al.Establishment of the Optimum ISSR-PCR Reaction System of Cypripedium in the Region of Changbai Mountain of China[J].Northern Horticulture,2013,37(14):92.
备注/Memo
第一作者简介:赵琬玥(1993-),女,硕士研究生,研究方向为分子生物学。E-mail:445994187@qq.com.责任作者:屈燕(1979-),女,博士,副教授,现主要从事园林植物资源保护与开发利用的教学与科研等工作。E-mail:flyersw@163.com.基金项目:国家自然科学基金资助项目(31460218);云南省高校重点建设学科(风景园林学)建设资助项目(云学位[2011]16号);国家级质量工程园林专业综合改革试点资助项目(50126002)。收稿日期:2018-03-01