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RAPD Analysis on Three Cucurbita ficifotia(PDF)

《北方园艺》[ISSN:1001-0009/CN:23-1247/S]

Issue:
2015年17
Page:
75-78
Research Field:
Publishing date:

Info

Title:
RAPD Analysis on Three Cucurbita ficifotia
Author(s):
CHENG Xiaojing1ZHOU Chuqi1ZHOU Liying1BU Lulu1HONG Jiankang2YANG Zhengan1
(1.College of Horticulture,Yunnan Agricultural University,Kunming,Yunnan 6502101;2.Honghe Prefecture Agricultural Institute of Yunnan Province,Mengzi,Yunnan 661100)
Keywords:
Cucurbita ficifotia Bauchegenome DNARAPDgenetic diversity
PACS:
-
DOI:
10.11937/bfyy.201517019
Abstract:
The genomic DNA of 3 Cucurbita ficifotia whose names were ‘Green peel’,‘White peel’ and ‘Green peel with White peel’ respectively were extracted by CTAB and were used to analysis the genetic relationships by RAPD molecular markers.RAPD was affected by many factors,so this experiment was for improved RAPD method.5 factors and 4 levels orthogonal design and screening of RAPD-PCR reaction system was used,the three kinds of black seed pumpkin relatedness were analyzed.The results showed that from 38 kinds of random primers selected 20 kinds of primers,6 kinds of the primers’analysis was clear amplification,and better repeatability.Total 43 bands were amplified,in which 39 bands were polymorphic.The percentage of polymorphic band was 90.70%.The cluster analysis results were indicated as follows:the average genetic distance among ‘Green peel’,‘White peel’ and ‘Green peel with white spot’ was 0.94.The genetic distance between ‘White peel’ and ‘green peel with white spot’ was 0.40.The results showed that the Cucurbita ficifotia varieties of relationships:‘Green peel’ and ‘White peel’,‘Green peel with white spot’ had far more distant relatives,and then‘White peel’ and ‘Green peel with white spot’ had close genetic relationship.

References:

 

[1]赖众民.黑籽南瓜优异的种质资源[J].云南农业科技,1991(4):42-44.

[2]蒋有条,孙利祥,张明方.我国瓜类嫁接栽培的进展与展望[J].长江蔬菜,1998(6):1-4.

[3]缪珉.黄瓜热伤害与热适应生理机制及耐热栽培技术研究[D].南京:南京农业大学,2000.

[4]张菊平,张长远.碧绿3号苦瓜种子纯度的RAPD检测研究[J].广东农业科学,2002(4):18.

[5]WILLIAMS J C,KUBELIK A R,JENNER C E,et al.DNA polymorphisms amplified by arbitrary primers are useful as genetic markers[J].Nucl Acid Res,1990,18(6):531-535.

[6]WELSH JMCCLELLAND M.Fingerprinting genomes using PCR with arbitraty primers[J].Nucl Acid Res,1990,18(7):213-218.

[7]SCOTT V T,JOSEPH P Del Tufo.Genetic analysis with random amplified polymorphic DNA makers[J].Plant Phisiol,1993,101:349-352.

[8]CHENG F S,BROWN S K,WEEDEN N F.A DNA extraction protocol from various tissues in woody species[J].Hort Science,1997,32(5):921-922.

[9]VOS P,HOGERS R,BLEEKER M.AFLP:A new technique for DNA fingerprinting[J].Nucl Acids Res,1995,23:4407-4414.

[10]NEI M,LI W H.Mathematical model for studying genetic variation in terms of restriction endonucleases[J].Proc Natl Acad Sci USA,1979,76:5269-5273.

[11]胡润芳,薛珠政,唐永晖.白灵侧耳菌株间的RAPD分析[J].福建农业学报,2006,21(4):346-349.

[12]张建珍,郭亚平,张敏,.云南三种稻蝗基因组DNARAPD多态性分析[J].动物分类学报,2005,30(3):447-452.

[13]CUI X M.Authentication of Panax notoginseng by 5S-rRNA spacer domain and random amplified polymorphic DNA(RAPD)analysis[J].Planta M ed,2003,69(6):584-586.

[14]PARK S Y,YOOK C S,NOHARA T,et al.Random amplified polymorphic DNA analysis of genetic relationships among Acanthopanax species [J].Arch Pharm Res,2004,27(12):1270-1274.

[15]HOSOKAWA K,MINAMI M,KAWAHARA K,et al.Discrimination among three species of medicinal Scutellaria plants using RAPD markers [J].Planta M ed,2000,66(3):270-272.

[16]ZHANG M,HUANG H R,LIAO S M,et al.Cluster analysis of Dendrobium by RAPD and design of specific pri mer for Dendrobium candidum[J].China J Chin Med Mater,2001,26(7):442-447.

[17]WANG A M,JI S.Experi ment briefing of two officinal Dendrobium by RAPD [J].J Chin Med Mater2002,25(5):324-325.

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Last Update: 2015-10-10