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Two yield-enhancing genes (yld1.1 and yld2.1) are located on chromosomes 1 and 2 respectivelyin a weedy relative of cultivated rice, Oryza rufipogon. SSR markers RM9 and RM166 are closelylinked with the two loci respectively. Minghui63 (MH63) has been a widely used restorationline in hybrid rice production in China during the past two decades. The F1 of cross “MH63O.rufipogon” was backcrossed with MH63 generation by generation. RM9 and RM166 were used toselect the plants from the progeny of the backcross populations. The results were as follows:(1) In BC2F1 population, the percentage of the individuals which have RM9 and RM166 amplifiedbands simultaneously was 12.2%, while in the BC3F1 population, that was 16.3%. (2) Among 400individuals of BC3F1, four yield-promising plants were obtained, with yield being 30% more thanthat of MH63. (3) The products amplified by primer RM166 in O. rufipogon and MH63 weresequenced. It was found that the DNA fragment sequence amplified by RM166 from MH63 was 101 bpshorter than that from O. rufipogon. The 101bp sequence is a part of an intron of the PCNA(proliferating cell nuclear antigen) gene.
Two yield-enhancing genes (yld1.1 and yld2.1) are located on chromosomes 1 and 2 respectively in a weedy relative of cultivated rice, Oryza rufipogon. SSR markers RM9 and RM166 are closely linked with the two loci respectively. Minghui63 (MH63) has was a widely used restorationline in hybrid rice production in China during the past two decades. The F1 of cross “MH63O.rufipogon” was backcrossed with MH63 generation by. RM9 and RM166 were used toselect the plants from the progeny of the backcross populations. The results were as follows: (1) In BC2F1 population, the percentage of the individuals which have RM9 and RM166 amplified bands simultaneously was 12.2% while in the BC3F1 population, that was 16.3%. (2) Among 400 individuals of BC3F1, (3) The products amplified by primer RM166 in O. rufipogon and MH63 were sequenced. It was found that the DNA fragment sequence amplified by RM166 from MH 63 was 101 bp shorter than that from O. rufipogon. The 101 bp sequence is a part of an intron of the PCNA (proliferating cell nuclear antigen) gene.