Rice contains several MADS box genes. It has been demonstrated previously that one of these genes, OsMADS1 (for Oryza sativa MADS box gene1 ), is expressed preferentially in flowers and causes early flowering when ectopically expressed in tobacco plants. In this study, we demonstrated that ectopic expression of OsMADS1 in rice also results in early flowering. To further investigate the role of OsMADS1 during rice flower development, we generated transgenic rice plants expressing altered OsMADS1 genes that contain missense mutations in the MADS domain. There was no visible alteration in the transgenic plants during the vegetative stage. However, transgenic panicles typically exhibited phenotypic alterations, including spikelets consisting of elongated leafy paleae and lemmas that exhibit a feature of open hull, two pairs of leafy palea-like and lemma-like lodicules, a decrease in stamen number, and an increase in the number of carpels. In addition, some spikelets generated an additional floret from the same rachilla. These characteristics are very similar to those of leafy hull sterile1 ( lhs1 ). The map position of OsMADS1 is closely linked to that of lhs1 on chromosome 3. Examination of lhs1 revealed that it contains two missense mutations in the OsMADS1 MADS domain. A genetic complementation experiment showed that the 11.9-kb genomic DNA fragment containing the wild-type OsMADS1 gene rescued the mutant phenotypes. In addition, ectopic expression of the OsMADS1 gene isolated from the lhs1 line resulted in lhs1 -conferred phenotypes. These lines of evidence demonstrate that OsMADS1 is the lhs1 gene.
INTRODUCTIONIn response to floral induction, the inflorescence meristem becomes committed to flowering. LEAFY ( LFY ) and APE-TALA1 ( AP1 ) in Arabidopsis and FLORICAULA ( FLO ) and SQUAMOSA ( SQUA ) in Antirrhinum are responsible for promoting the specification of floral meristem identity (reviewed in Ma, 1994). The genes required for specifying the fate of floral organ primordia include AP1 , AP2 , AGAMOUS ( AG ), PISTILATA ( PI ), and AP3 in Arabidopsis and SQUA , PLENA ( PLE ), GLOBOSA ( GLO ), and DEFICIENS ( DEF ) in Antirrhinum (reviewed in Weigel and Meyerowitz, 1994). Excluding AP2 , these floral homeotic genes encode MADS box proteins that are highly conserved transcription factors in plants, animals, yeast, and fungi and that are regulated by the floral meristem identity gene LFY (Parcy et al., 1998;Wagner et al., 1999).Several other MADS box genes have more subtle functions associated with floral meristem and floral organ identity. Expression of AG-LIKE2 ( AGL2 ), AGL4 , and AGL9 of Arabidopsis begins after the onset of expression of floral meristem identity genes but before the activation of floral organ identity genes (Flanagan and Ma, 1994;Savidge et al., 1995;Mandel and Yanofsky, 1998). DEFH72 and DEFH200 of Antirrhinum appear to function in mediating interactions between the meristem and organ identity genes through direct interaction with PLE (Davies et al., 1996). FLORAL BINDING PROTEIN2 ( FBP2 ) o...