您好,欢迎访问浙江省农业科学院 机构知识库!

Salinity tolerant performance and genetic diversity of four rice varieties

文献类型: 外文期刊

作者: Xie, JH 1 ; Zapata-Arias, FJ 2 ; Shen, M 2 ; Afza, R 2 ;

作者机构: 1.Int Atom Energy Agcy Labs, FAO IAEA Agr & Biotechnol Lab, Plant Breeding Unit, A-2444 Seibersdorf, Austria

2.Int Atom Energy Agcy Labs, FAO IAEA Agr & Biotechnol Lab, Plant Breeding Unit, A-2444 Seibersdorf, Austria; Zhejiang Agr Univ, Inst Nucl Agr Sci, Hangzhou 310029, Peoples R China; Zhejiang Acad Agr Sci, Inst Applicat Atom Energy, Hangzhou 310021, Peoples R China

关键词: PCR;RAPDS;rice;salt-tolerance

期刊名称:EUPHYTICA ( 影响因子:1.895; 五年影响因子:2.181 )

ISSN: 0014-2336

年卷期: 2000 年 116 卷 2 期

页码:

收录情况: SCI

摘要: The genetic diversity of three salinity tolerant rice varieties Pokkali, Nona-Bokra and Bicol was investigated using random amplified polymorphic DNAs (RAPDs). Hi,oh yielding susceptible variety IR29 was used as check for comparison. The salinity performance of these varieties were tested by using rapid screening techniques at seedling stage. One hundred primers tested of which 42 revealed differences between Pokkali & Nonabokra, 43 between Pokkali st Bicol and 50 between Nonabokra and Bicol. Polymorphism differences between IR29 - Pokkali, IR29 - NonaBokra and IR29 - Bicol were 47%, 53% and 31%, respectively. Four primers amplified specific fragments that appeared in all the three salt tolerant varieties but not in the salt susceptible variety IR 29. Primer UBC 9 (5'-CCTGCGCTTA-3') produced a prominent diagnostic fragment of approximately 1600 bp; primer UBC 244 (5'-CAGCCAACCG-3') generated a fragment of about 800 bp in the salt-tolerant varieties; primer UBC 251 (5'-CTTGACGGGG-3') amplified one polymorphic band of 1100 bp and primer UBC 267 (5'-CCATCTTGTG-3') yielded a relatively weak polymorphic band of 1100 bp.

  • 相关文献

[1]Putrescine Plays a Positive Role in Salt-Tolerance Mechanisms by Reducing Oxidative Damage in Roots of Vegetable Soybean. Zhang Gu-wen,Xu Sheng-chun,Hu Qi-zan,Gong Ya-ming,Mao Wei-hua. 2014

[2]Modeling and Analyzing the Influence of Blade Shape on Rice Canopy Structure. Liyong Cao,Dong Li,Junmin Wang,Zhigang Zhan. 2012

[3]Modeling and analyzing the influence of blade shape on rice canopy structure. Li, Dong,Wang, Junmin,Zhan, Zhigang,Cao, Liyong. 2012

[4]Mapping of leaf and neck blast resistance genes with RFLP, RAPD and resistance gene analogs in rice. K.-L. ZHENG,R.-Y. CHAI,M.-Z. JIN,J.-L. WU,Y.-Y. FAN,H. LEUNG,J.-Y. ZHUANG. 2000

[5]Monitoring Leaf Chlorophyll Fluorescence with Spectral Reflectance in Rice (Oryza sativa L.). Hao Zhang,Lian-feng Zhu,Hao Hu,Ke-feng Zheng,Qian-yu Jin. 2011

[6]DEVELOPMENT AND APPLICATION OF THE CONSULTING SYSTEM OF PRECISION FERTILIZATION IN RICE. Xiaonan Lii,Wanzhu Ma,Zhouqiao Ren,Xiaojia Chen. 2005

[7]Effects of Nitrogenous Fertilization in Rice Fields on the Predatory Function ofCyrtorhinus Lividipennis to Nilaparvata lugens Stal. LU Zhongxian,YU Xiaoping,HEONG Kongluen,HU Cui. 2008

[8]梨火疫病菌新的Ⅲ型泌出系统(T3SS)分析及在其他菌株中的分布. 柴一秋,BOCSANCZY Ana Maria,BEER Steven,王金生. 2010

[9]浙江柑橘黄龙病病原β-操纵子核糖体蛋白基因的PCR检测及其序列比对. 张利平,陈国庆,王海琴,黄振东. 2010

[10]台州地区规模猪场主要疫病的流行病学调查. 徐丽华,陈冬祥,姚邦,候贤宏,游新根,管妙东,王一成. 2017

[11]柑桔黄龙病菌分子生物学研究进展. 张利平. 2007

[12]猪圆环病毒2型PCR检测方法的建立. 李婧雅,王德全,袁秀芳,黄华荣. 2018

[13]鸡粪便来源大肠杆菌的质谱法快速鉴定及聚类分析. 张玲,常江,曹刘杰,杨华,夏效东,唐标. 2018

[14]CaMV35S启动子及其在转基因作物中的应用和检测. 汤婷,谢实龙,祝旋,徐俊锋,唐俊,汪小福. 2019

[15]牛羊线虫抗药性及其PCR检测技术研究进展. 李国勤,张雪娟. 2002

[16]应用PCR方法检测烟粉虱传双生病毒. 叶青静,杨悦俭,王荣青,李志邈,阮美颖,周国治,姚祝平. 2008

[17]家蚕磷酸甘油醛异构酶Tpi基因的克隆. 牛宝龙,孟智启,翁宏飙,沈卫锋,吕顺霖. 2005

[18]转基因大豆SHZD32-1转化体普通PCR和qRT-PCR检测方法的研究. 杨华,彭城,肖英平,汪小福,徐俊锋. 2018

[19]蟹源易损气单胞菌气溶素基因的克隆及其PCR检测. 徐海圣,曾健,徐步进. 2008

[20]兔支气管败血波氏杆菌的分离鉴定及耐药基因检测. 王晓芳,刘燕,肖琛闻,鲍国连,崔言顺,李建亮,季权安,韦强. 2015

作者其他论文 更多>>