|Table of Contents|

Establishment of ISSR Reaction System and Genetic Diversity Analysis of Hypericum attenuatum Choisy.(PDF)

《北方园艺》[ISSN:1001-0009/CN:23-1247/S]

Issue:
2017年05
Page:
96-101
Research Field:
Publishing date:

Info

Title:
Establishment of ISSR Reaction System and Genetic Diversity Analysis of Hypericum attenuatum Choisy.
Author(s):
WANG Xia12XU Jize12WANG Huan12GAO Qianqian1
(1.College of Biological Engineering,College of Jilin Agriculture Science and Technology,Jilin,Jilin 132101;2.Key Laboratory of Changbai Mountain Animal and Plant Rescources′ Utilization and Protection of Universities in Jilin Province,Jilin,Jilin 132101)
Keywords:
Hypericum attenuatumISSR reaction systemgenetic diversity
PACS:
-
DOI:
10.11937/bfyy.201705023
Abstract:
Fourteen Hypericum attenuatum were used as materials,the ISSR-PCR reaction system was established and optimized by L16(45) orthogonal experimental design.The genetic diversity of Hypericum attenuatum was analyzed by the optimal reaction system.The results showed that the optimum reaction system contained 1.0 U Taq DNA polymerase,0.2 mmol?L-1 dNTs,2.0 mmol?L-1 Mg2+ and 45 ng DNA template respectively in a 20 μL ISSR reaction system.Eleven polymorphic primers which were used to analyze the genetic diversity of Hypericum attenuatum were selected from 45 ISSR primers.A total of 85 bands were amplified,of which 57 bands were polymorphic loci and the percentage of total polymorphic loci was 67.06%.The genetic similarity coefficient was 0.375 1-0.725 2 in 4 populations of Hypericum attenuatum,and the average was 0.541 6.The clustering analysis was constructed by UPGMA method based on the genetic identity and 14 Hypericum attenuatum materials were clustered into 3 main groups and 4 subgroups.The level of genetic diversity of Hypericum attenuatum between populations was higher than that within populations and between the genetic distance and geographic distance had a certain correlation.

References:

 

[1]李冀,吴全娥,高彦宇,.鼠海马单胺类神经递质含量5-HT5-HIAA的影响[J].中医药信息,2012,29(5):18-20.

[2]李冀,曹明明,高彦宇.乌腺金丝桃与丹参配伍对心肌缺血模型动物影响的研究[J].中医药学报,2012,40(1):17-19.

[3]孟祥丽,赵玉佳,徐艳敏,.黑龙江省乌腺金丝桃资源学调查[J].中国野生植物资源,2014,33(3):56-57.

[4]张艳艳,郭庆梅,周凤琴,.分子标记技术在木瓜属种质资源研究中的应用[J].辽宁中医药大学学报,2015,7(12):60-62.

[5]白玉.DNA分子标记技术及其应用[J].安徽农业科学,2007,35(24):7422-7424.

[6]牛俊海,黄少华,冷青云,.分子标记技术在红掌研究中的应用与展望[J].分子植物育种,2015,13(6):1424-1432.

[7]ZIETKIEWICZ ERAFALSKI ALABUDA D.Genome fingerprinting by simple sequence repeat(SSR)-anchored polymerase chain reaction amplification[J].Genonics,1994,20(2):176-183.

[8]王超,张智勇,陈永胜,.ISSR分子标记技术及其在蓖麻遗传育种中的应用[J].黑龙江农业科学,2012(9):14-17.

[9]邓汉超,王学林,李筠,.正交优化水稻ISSR种质鉴定技术研究[J].中国种业,2012(12):48-50.

[10]刘楠楠,薛运波,王志,.蜜蜂遗传多样性研究的RAPD-PCR反应体系的正交优化[J].吉林畜牧兽医,2011,9(32):4-7.

[11]吴生,熊宇婷,谢砚,.正交设计优化翼梗五味子ISSR-PCR反应体系[J].中草药,2011,42(5):976-979.

[12]靳晓丽,田新会,杜文华.鹰嘴豆ISSR应体系的正交优化[J].草地学报,2015,23(6):1303-1309.

[13]唐辉,陈宗游,史艳财,.正交设计优化地枫皮ISSR-PCR反应体系[J].中草药,2013,44(5):610-615.

[14]赵博,李景剑,符支宏,.正交设计优化大旗瓣凤仙ISSR-PCR反应体系[J].南方农业学报,2014,45(2):184-188.

[15]任风鸣,金江群,焦雁翔,.中药金钱草种质资源的ISSR遗传多样性研究[J].中国药学杂志,2015,50(15):1277-1281.

[16]李卫星,花艳敏,张秀萍,.银杏雄株ISSR分子标记及亲缘关系分析[J].扬州大学学报(农业与生命科学版),2015,36(1):101-106.

[17]汤正辉,祝亚军,谭晓风,.河南连翘种群遗传多样性的ISSR分析[J].中南林业科技大学学报,2013,33(8):32-37.

[18]周冬琴,莫海波,芦治国.基于SRAP标记的墨西哥落羽杉优良单株的遗传多样性分析[J].植物资源与环境学报,2012,21(1):36-41.

Memo

Memo:
-
Last Update: 2017-03-24