|Table of Contents|

Optimization of ISSR Amplification Conditions in Ancient Camphor-trees(PDF)

《北方园艺》[ISSN:1001-0009/CN:23-1247/S]

Issue:
2013年07期
Page:
116-120
Research Field:
Publishing date:

Info

Title:
Optimization of ISSR Amplification Conditions in Ancient Camphor-trees
Author(s):
HUANG Meng12CHEN Shang-xing12YANG Guang-yao12WANG Zong-de12JI Chun-feng12
1.College of Landscape and Art,Jiangxi Agricultural University,Nanchang,Jiangxi 330045;
2.Jiangxi Provincial Key Laboratory for Bamboo Germplasm Resources and Applications,Jiangxi Agricultural University,Nanchang,Jiangxi 330045
Keywords:
ancient camphor-treesISSRreaction conditionoptimization
PACS:
S 792.23
DOI:
-
Abstract:
The genomic DNA of ancient camphor-trees was extracted from leaves by improved CTAB method.With the design of single factor experiment method,the influences of seven factors including Mg2+,dNTP,DNA content in the template,Taq DNA polymerase,amounts of primer,deionized formamide,and annealing temperature on PCR amplification were analyzed.The results showed that the best ISSR-PCR reaction system of ancient camphor-trees was as follows:50 ng DNA template,2.5 mmol/L MgCl2,0.20 mmol/L dNTPS,1.0 U Taq polymerase,0.5 μmol/L primer and 2% formamide deionized in 20 μL reaction volume.The results would lay a technology foundation for further study of the genetic diversity of ancient camphor-trees with ISSR molecular marking.

References:

[1]中国树木志编辑委员会.中国树木志(第一卷)[M].北京:中国林业出版社,1983:735-749.

[2]李明志.江西古树[M].南昌:江西人民出版社,1998:61-68.

[3]邢建宏,刘希华,陈存及,.樟树几种生化类型及近缘种的RAPD分析[J].三明学院学报,2007,24(4):433-437.

[4]邢建宏,陈存及,张国防.樟树ISSR-PCR反应体系优化研究[J].福建林业科技,2006,33(3):96-98.

[5]邢建宏,陈存及,张国防,.樟树几种化学类型及近缘种的ISSR分析[J].福建林业科技,2008,35(4):101-104.

[6]宋爱云,陈辉,董林水.RAPD分子标记在鉴定香樟优选株和普通株中的应用[J].应用与环境生物学报,2009,9(3):263-265.

[7]Zietkiewicz ERafalak I ALabud Aet al.Genome fingerprinting by simple sequence repeat (SSR)-anchored polymerase chain reaction amplification[J].Genomic,1994,20(2):176-183.

[8]Iruela MRubio JCubero J Iet al.Phylogenetic analysis in genus Cicer and cultivated chickpea using RAPD and ISSR markers[J].Theor Appl Genet,2002,104:643-651.

[9]Debnath S C.Inter-simple sequence repeat (ISSR)-PCR analysis to assess genetic diversity in a collection of wild cloudberry (Rubus chamaemorus?L.) clones[J].Journal of Horticultural Science and Biotechnology,2007,82(5):727-732.

[10]Li AGe S.Genetic variation and colonal diversity of Psammochloa villosa?(Poaceae) detected by ISSR markers[J].Ann Bot,2001,87:585-590.

[11]Esselman E JLi J QCrawford D Jet al.Clonal diversity in the rare Calamagrostis porteri ssp.insperata?(Poaceae)comparative results for allozymes and random amplified polymorphic DNA (RAPD) and inter simple sequence repeat (ISSR) markers[J].Mol Ecol,1999,8:443-451.

[12]Ammiraju J S SDholakia B BSantra D Ket al.Identification of inter simple sequence repeat (ISSR) markers associated with seed size in wheat[J].Theor Appl Genet,2001,102:726-732.

[13]Hao G,Lee D H,Lee J S,et al.A study of taxonomical relationships among species of Korean?Allium?sect.Sacculiferum?(Alliaceae) and related species using inter-simple sequence repeat (ISSR) markers[J].Bot Bull Acad Sin,2002,43:63-68.

[14]Prevost AWilkinson M J.A new system of comparing PCR primers applied to ISSR fingerprinting of potato cultivars[J].Theor Appl Genet,1999,98:107-112.

[15]Bornet BBranchard M.Nonanchored inter simple sequence repeat (ISSR) markersreproducible and specific tools for genome fingerprinting[J].Plant Molecular Biology Reporter,2001,19:209-215.

[16]王国霞,曹福亮,方炎明.古银杏雄株的ISSR遗传多样性分析[J].北京林业大学学报,2010,32(2):39-45.

[17]金则新,李均敏.濒危植物夏腊梅扩增条件的优化[J].植物研究,2007,27(1):69-72.

[18]张国防,陈存及,邢建宏.樟树干叶DNA提取方法的研究[J].江西农业大学学报,2006,28(1):111-114.

[19]卢圣栋.现代分子生物学实验技术[M].2.北京:中国协和医科大学出版社,1999:458-463.

[20]温强,叶金山,雷小林,.油茶ISSR反应体建立及优化[J].中南林学院学报,2006,26(6):22-26.

[21]钱韦,葛颂,洪德元.采用RAPDISSR标记探讨中国疣粒野生稻的遗传多样性[J].植物学报,2000,42(7):741-750.

[22]Joshi S PGupta V SAggarwal R Ket al.Genetic diversity and phylogenetic relationship as revealed by inter simple sequence repeat (ISSR) polymorphism in the genus?Oryza[J].Theor Appl Genet,2000,100:1311-1320.


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Last Update: 2014-08-24