An exploratory study on allelic diversity among rice and its wild species as well as relatives with simple sequence repeat and inter simple sequence repeat markers

被引:0
|
作者
Ganie, Showkat Ahmad [1 ,2 ]
Karmakar, Joydip [1 ]
Roychowdhury, Rajib [1 ]
Mondal, Tapan Kumar [2 ]
Dey, Narottam [1 ]
机构
[1] Visva Bharati, Dept Biotechnol, Santini Ketan 731235, W Bengal, India
[2] Natl Bur Plant Genet Resources, Div Genom Resources, New Delhi 110012, India
来源
INDIAN JOURNAL OF BIOTECHNOLOGY | 2016年 / 15卷 / 03期
关键词
Genetic diversity; ISSR; rice; SSR; wild rice; ORYZA-SATIVA L; COARCTATA ROXB. TATEOKA; GENETIC DIVERSITY; SALT-TOLERANCE; INTROGRESSION; LANDRACES;
D O I
暂无
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Genomic information of crop plants is a pre-requisite for the enrichment and management of the crop's genetic resources. Rice has a number of wild species and wild relatives, which harbdur a good number of agronomically important genes that can be incorporated into the cultivated rice. In the present work, a wild rice (Oryza rufipogon Griff.) and a wild rice relative, Porteresia coarctata (Roxb.) Tateoka (syn. O. coarctata Roxb.), were genotyped with trait (osmotic stress tolerance) linked 29 SSR and 22 ISSR markers, distributed throughout the rice genome. For exploring the comparative allelic diversity (in the form of difference in mol wt of amplified products for a particular SSR or ISSR locus), two marker based panels were constructed considering cultivated rice (O. saliva L.) as the reference genotype. Among the studied SSR markers, the maximum allelic variation was found with RM10773, which showed the maximum difference (370.25 bp) between O. saliva and O. rufipogon, and also with RM10864 that showed a difference of 194.47 bp between O. sativa and P. coarctata. For ISSR loci, the maximum difference (300.73 bp) between O. saliva and O. rufipogon was shown by PR36, and the maximum difference (451.66 bp) between O. saliva and P. coartata was shown by PR29. The genotypic profiles prepared in the present investigation may be used for identification of the corresponding genotypes and in marker assisted hybridization programmes.
引用
收藏
页码:357 / 362
页数:6
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