Development of a SCAR marker linked with a MYMV resistance gene in mungbean ( V igna radiata L. W ilczek)
Vinod Janardan Dhole, Kandali Sreenivasulu Reddy
Abstract
Vinod Janardan Dhole, Kandali Sreenivasulu Reddy
Abstract
Abstract Yellow mosaic disease (YMD) caused by mungbean yellow mosaic virus (MYMV) is the most important disease of mungbean, causing great yield loss. The present investigation was carried out to study the inheritance and identify molecular markers linked with MYMV resistance gene by using F1, F2 and 167 F2 : 8 recombinant inbred lines (RILs) developed from the cross ‘TM‐99‐37’ (resistant) × Mulmarada (susceptible). The F1 was susceptible, F2 segregated in 3S:1R phenotypic ratio and RILs segregated in 1S:1R ratio in the field screening indicating that the MYMV resistance gene is governed by a single recessive gene. Of the 140 RAPD primers, 45 primers showing polymorphism in parents were screened using bulked segregant analysis. Three primers amplified specific polymorphic fragments viz. OPB‐07600, OPC‐061750 and OPB‐12820. The marker OPB‐07600 was more closely linked (6.8 cM) with a MYMV resistance gene as compared to OPC‐061750 (22.8 cM) and OPB‐12820 (25.2 cM). The resistance‐specific fragment OPB‐07600 was cloned, sequenced and converted into a sequence‐characterized amplified region (SCAR) marker and validated in twenty genotypes with different genetic backgrounds.
OpenAlex reports 34 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Abstract Yellow mosaic disease (YMD) caused by mungbean yellow mosaic virus (MYMV) is the most important disease of mungbean, causing great yield loss. The present investigation was carried out to study the inheritance and identify molecular markers linked with MYMV resistance gene by using F1, F2 and 167 F2 : 8 recombinant inbred lines (RILs) developed from the cross ‘TM‐99‐37’ (resistant) × Mulmarada (susceptible). The F1 was susceptible, F2 segregated in 3S:1R phenotypic ratio and RILs segregated in 1S:1R ratio in the field screening indicating that the MYMV resistance gene is governed by a single recessive gene. Of the 140 RAPD primers, 45 primers showing polymorphism in parents were screened using bulked segregant analysis. Three primers amplified specific polymorphic fragments viz. OPB‐07600, OPC‐061750 and OPB‐12820. The marker OPB‐07600 was more closely linked (6.8 cM) with a MYMV resistance gene as compared to OPC‐061750 (22.8 cM) and OPB‐12820 (25.2 cM). The resistance‐specific fragment OPB‐07600 was cloned, sequenced and converted into a sequence‐characterized amplified region (SCAR) marker and validated in twenty genotypes with different genetic backgrounds.
Key concepts: Biology, RAPD, Bulked segregant analysis, Vigna, Gene, Genotype, Genetic marker, Genetics