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Genetic analysis of rolled leaf is important to rice ideotype breeding.To detect loci controlling rolled leaf of japonica restorer lines,SSR marker genotypes and phenotypes of flag leaf rolling index(LRI) were investigated in Xiushui 79(P1,a japonica rice variety),C Bao(P2,a japonica restorer line) and 254 recombinant inbred lines derived from the cross between P1 and P2,and in two environments.A genetic map of this cross was constructed,QTLs for LRI were detected and their interactions with environments were analyzed.Among 818 pairs of SSR primers,90 primers showed polymorphism between P1 and P2,and 12 markers showed highly significant correlation with LRI in both environments based on single marker regression analysis.The genetic map containing 74 information loci has a total distance of 744.6 cM,with an average of 10.1 cM between two adjacent loci.Three QTLs(qRL-1,qRL-7 and qRL-8-1) were detected with two softwares:WinQTLCart 2.5 and QTLNetwork2.0.qRL-8-1 was a new locus,accounting for 15.5% and 12.8% of phenotypic variations in the two environments,respectively.The phenotypic variation explained by additive effect was 6.6%.No interaction was found between qRL-8-1 genotype and environments.
Genetic analysis of rolled leaf is important to rice ideotype breeding. To detect loci controlled rolled leaf of japonica restorer lines, SSR marker genotypes and phenotypes of flag leaf rolling index (LRI) were investigated in Xiushui 79 (P1, a japonica rice variety) C Bao (P2, a japonica restorer line) and 254 recombinant inbred lines derived from the cross between P1 and P2, and in two environments. A genetic map of this cross was constructed, QTLs for LRI were detected and their interactions with environments were analyzed . Amm 818 pairs of SSR primers, 90 primers showed polymorphism between P1 and P2, and 12 markers showed highly significant correlation with LRI in both environments based on single marker regression analysis. The genetic map containing 74 information loci has a total distance of 744.6 cM , with an average of 10.1 cM between two adjacent loci.Three QTLs (qRL-1, qRL-7 and qRL-8-1) were detected with two softwares: WinQTLCart 2.5 and QTLNetwork2.0.qRL-8-1 was a new locus, accounting for 15.5% and 12.8% of phenotypic variations in the two environments, respectively. The phenotypic variation explained by additive effect was 6.6% .No interaction was found between qRL-8-1 genotype and environments.