2011
DOI: 10.4238/vol10-3gmr1331
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Analysis of simple sequence repeat markers linked with blast disease resistance genes in a segregating population of rice (Oryza sativa)

Abstract: ABSTRACT. Among 120 simple sequence repeat (SSR) markers, 23 polymorphic markers were used to identify the segregation ratio in 320 individuals of an F 2 rice population derived from Pongsu Seribu 2, a resistant variety, and Mahsuri, a susceptible rice cultivar. For phenotypic study, the most virulent blast (Magnaporthe oryzae) pathotype, P7.2, was used in screening of F 2 population in order to understand the inheritance of blast resistance as well as linkage with SSR markers. Only 11 markers showed a good fi… Show more

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Cited by 43 publications
(38 citation statements)
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“…Plant material and crossing scheme BC 2 F 1 population derived from a cross between resistant rice variety, Pongsu Seribu 2, and the susceptible variety MR219 was genotyped with selected SSR markers tightly linked to blast resistance genes (Ashkani et al 2011). The general backcrossing steps were followed until BC 2 F 1 population.…”
Section: Methodsmentioning
confidence: 99%
“…Plant material and crossing scheme BC 2 F 1 population derived from a cross between resistant rice variety, Pongsu Seribu 2, and the susceptible variety MR219 was genotyped with selected SSR markers tightly linked to blast resistance genes (Ashkani et al 2011). The general backcrossing steps were followed until BC 2 F 1 population.…”
Section: Methodsmentioning
confidence: 99%
“…The gels were documented using Alpha Imager 1220 (Alpha Innotech, CA, USA). Microsatellite or Simple sequence repeat (SSR) markers were used for the rice lines selection (Temnykh et al, 2001;McCouch et al, 2002;Ashkani et al, 2011).…”
Section: Polymerase Chain Reaction (Pcr)mentioning
confidence: 99%
“…The four-leaf stage seedlings were placed in inoculation chambers and inoculated with a conidial suspension (5 x 10 4 conidia/ mL). The inoculated plants were kept in the chambers at 26°C with 95% relative humidity and darkness for 24 h. They were then transferred to the greenhouse (28°-30°C/day and 20°-22°C/ night) for disease incubation, at 100% relative humidity, by intermittently spraying water for 1-2 min every 2 h (Ashkani et al, 2011). Each line was inoculated in two independent experiments, and three replications were conducted for each experiment.…”
Section: Pathogen Inoculation and Disease Evaluationmentioning
confidence: 99%