首页 | 本学科首页   官方微博 | 高级检索  
     


Screening and identification of random amplified polymorphic DNA (RAPD) markers linked to mungbean yellow mosaic virus (MYMV) resistance in mungbean (Vigna radiata (L.) Wilczek)
Authors:A. Karthikeyan  M. Sudha  N. Senthil  M. Pandiyan  M. Raveendran  P. Nagrajan
Affiliation:1. Department of Plant Molecular Biology &2. Biotechnology , Centre for Plant Molecular Biology, Tamil Nadu Agricultural University Coimbatore , India karthik2373@gmail.com;4. Biotechnology , Centre for Plant Molecular Biology, Tamil Nadu Agricultural University Coimbatore , India;5. National Pulses Research Centre , Tamil Nadu Agricultural University , Vamban , Pudhukottai , India
Abstract:Bulk segregant analysis (BSA) and random amplified polymorphic DNA (RAPD) techniques were used to analyse the F2 individuals of susceptible VBN (Gg) 2 × resistant KMG 189 to screen and identify the molecular marker linked to mungbean yellow mosaic virus (MYMV) resistant gene in mungbean. Two DNA bulks namely resistant bulks and susceptible bulks were setup by pooling equal amount of DNA from five randomly selected plants of each disease response. A total of 72 random sequence decamer oligonucleotide primers were used for RAPD analysis. Primer OPBB 05 (5′-GGGCCGAACA-3′) generated OPBB 05 260 fragment in resistant parent and their bulks but not in the susceptible parent and their bulks. Co segregation analysis was performed in resistant and susceptible F2 individuals, it confirmed that OPBB 05 260 marker was tightly linked to mungbean yellow mosaic virus resistant gene in mungbean.
Keywords:mungbean  RAPD  bulk segregant analysis  MYMV
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号