摘要
We have analyzed a lax mutant that exhibits altered panicle architecture in rice. The primary and secondary rachis-branches are normally initiated and each branch ends in a terminal spikelet, but all the lateral spikelets are absent and the terminal spikelet displays variegated structures in the mutant. An F2 population from the cross between the lax mutant and a japonica variety, W11, was constructed and analyzed. Using microsatellite and CAPS markers, the lax locus was mapped on the long arm of chromosome 1, co-segregated with a CAPS marker, LZ1, within an interval of 0.28 cM between a CAPS marker, HB2, and a microsatellite marker, MRG4389. RT-PCR analysis revealed that the expressions of the rice B-function MADS-box genes OsMADS2, OsMADS4, OsMADS16 and OsMADS3 were significantly reduced, whereas the expression of the rice A-function gene RAP1A was not altered.
We have analyzed a lax mutant that exhibits altered panicle architecture in rice. The primary and secondary rachis-branches are normally initiated and each branch ends in a terminal spikelet, but all the lateral spikelets are absent and the terminal spikelet displays variegated structures in the mutant. An F2 population from the cross between the lax mutant and a japonica variety, W11, was constructed and analyzed. Using microsatellite and CAPS markers, the lax locus was mapped on the long arm of chromosome 1, co-segregated with a CAPS marker, LZ1, within an interval of 0.28 cM between a CAPS marker, HB2, and a microsatellite marker, MRG4389. RT-PCR analysis revealed that the expressions of the rice B-function MADS-box genes OsMADS2, OsMADS4, OsMADS16 and OsMADS3 were significantly reduced, whereas the expression of the rice A-function gene RAP1A was not altered.
基金
This work was supported by the State High Technology Research and Development Project(Grant No.2001AA21108101).
